Mouse kidney development

The kidneys play a critical homeostatic role in the regulation of body fluid composition and excretion of waste products. Here I review our understanding of how the three different vertebrate kidney types (pronephros, mesonephros, and metanephros) arise during mouse development with a more comprehensive focus on the molecular regulation of metanephros formation. A detailed understanding of the genetic hierarchies governing renal development will provide insights into the pathogenesis of kidney disorders, advance efforts to direct pluripotent stem cells into therapeutically useful renal lineages in vitro, and further our understanding of renal regenerative pathways that occur in vivo. 1. Overview of kidney structure and embryonic development The kidneys are bilateral organs that regulate the composition and volume of the body fluids, and eliminate metabolic waste products. The filtering unit of the kidney is the nephron, which has a characteristic segmental organization. The glomerulus at the proximal end of the nephron filters the blood and passes the filtrate to a tubular epithelium that modifies it before delivering the urine to the collecting duct for disposal (see Figure 1). Mammalian renal development differs from that of most other organs in that it proceeds through a series of three successive phases, each marked by the formation of a more complex pair of kidneys. These kidneys, which are called the pronephros, mesonephros, and metanephros, develop in a cranial (anterior)-to-caudal (posterior) progression from stripes of mesodermal cells, called the intermediate mesoderm, that extend from the heart region to the tailbud of the embryo (see Figure 2). In amniotes (birds, mammals, and reptiles) the pronephros and the mesonephros are generally transient embryonic kidneys that subsequently degenerate and have little or no functionality. The metanephros, which persists as the definitive adult kidney, is characterized by an extensively branched collecting duct system and a large number of nephrons (∼11,000 in the mouse and 300,000–1 million in humans (Nyengaard and Bendtsen, 1992; Yuan et al., 2002). Structurally, the mammalian metanephros comprises an inner medullary region (containing collecting ducts and long loops of Henle—the nephron segment involved in urine concentration), an outer medullary region (containing short Loops of Henle and collecting ducts), and a cortical region (containing all other domains of the nephron; Figure 1). This gross structure is important for the functionality of the metanephric kidney as it establishes an osmotic gradient between the cortex and medulla that drives the extraction of water from the urine (Fenton and Knepper, 2007).


Overview of kidney structure and embryonic development
The kidneys are bilateral organs that regulate the composition and volume of the body fluids, and eliminate metabolic waste products.The filtering unit of the kidney is the nephron, which has a characteristic segmental organization.The glomerulus at the proximal end of the nephron filters the blood and passes the filtrate to a tubular epithelium that modifies it before delivering the urine to the collecting duct for disposal (see Figure 1).Mammalian renal development differs from that of most other organs in that it proceeds through a series of three successive phases, each marked by the formation of a more complex pair of kidneys.These kidneys, which are called the pronephros, mesonephros, and metanephros, develop in a cranial (anterior)-to-caudal (posterior) progression from stripes of mesodermal cells, called the intermediate mesoderm, that extend from the heart region to the tailbud of the embryo (see Figure 2).In amniotes (birds, mammals, and reptiles) the pronephros and the mesonephros are generally transient embryonic kidneys that subsequently degenerate and have little or no functionality.The metanephros, which persists as the definitive adult kidney, is characterized by an extensively branched collecting duct system and a large number of nephrons (∼11,000 in the mouse and 300,000-1 million in humans (Nyengaard and Bendtsen, 1992;Yuan et al., 2002).Structurally, the mammalian metanephros comprises an inner medullary region (containing collecting ducts and long loops of Henle-the nephron segment involved in urine concentration), an outer medullary region (containing short Loops of Henle and collecting ducts), and a cortical region (containing all other domains of the nephron; Figure 1).This gross structure is important for the functionality of the metanephric kidney as it establishes an osmotic gradient between the cortex and medulla that drives the extraction of water from the urine (Fenton and Knepper, 2007).Mouse kidney development begins with the formation of the pronephric duct (also known as the nephric or Wolffian duct; Figure 3).The nephric duct arises from the cranial portion of the intermediate mesoderm and grows caudally down the trunk to fuse with the urogenital sinus (ventral portion of the cloaca) at E11 (Hoar, 1976).As it migrates, the nephric duct induces the formation of mesonephric nephrons from the adjacent intermediate mesoderm (known as the nephrogenic cord or nephrogenic mesenchyme).Metanephros development is initiated at E10.5 at the caudal end of the nephric duct level with the hindlimb (27-28 th somite).Glial-derived growth factor (GDNF), secreted from a unique population of nephrogenic cells called the metanephric mesenchyme, induces an outgrowth from the nephric duct called the ureteric bud (UB) that then invades the metanephric mesenchyme (see Figure 3).The UB forms a T-shaped bifurcation at E11.5, and then undergoes ∼11 cycles of branching and elongation to generate the metanephric collecting duct system (Cebrian et al., 2004).During this process, each UB tip is surrounded by a cap of metanephric mesenchyme, a subset of which give rise to nephron progenitors that proliferate, differentiate into glomerular and tubular epithelial cells, and fuse with the collecting duct.Early studies demonstrated that reciprocal and inductive signaling between the UB and the metanephric mesenchyme are essential for initiating and maintaining the cycles of UB branching and nephron induction that underlie the formation of the metanephros (Grobstein, 1955;Grobstein, 1956).

Structure and function of the nephron
The glomerulus is the most proximal component of the nephron and comprises a capillary tuft surrounded by highly specialized epithelial cells called podocytes (Quaggin and Kreidberg, 2008).Podocytes have a unique morphology that is characterized by several large primary projections, each of which is branched into smaller secondary extensions that branch again into a 'comb-like' array of 'foot processes'.The foot processes from neighboring podocytes interdigitate, generating a series of narrow slits that are bridged by the slit diaphragm-a 'protein zipper' created by interactions between integral membrane proteins originating from adjacent foot processes.The foot processes are anchored to a specialized basal lamina, called the glomerular basement membrane (GBM), which also serves to separate the podocytes from the underlying endothelium.The endothelial cells of the glomerular capillary tuft are fenestrated, thus providing plasma solutes access to the GBM and slit diaphragm.Together, the fenestrated endothelium, GBM, and slit-diaphrgam make up the glomerular filter and function to retain high molecular weight proteins and blood cells in the circulation while allowing small molecules such as water, sugars, and electrolytes to enter the nephron (Quaggin and Kreidberg, 2008).
Once the filtrate has passed through the glomerular filter it encounters the first (proximal) portion of the tubule (see Figure 1).The proximal tubule is responsible for reabsorbing the majority of the filtrate, as it comprises metabolically useful solutes (Ullrich et al., 1963).The intermediate and the distal segments of the tubule further fine-tune the composition of the filtrate and play an important role in regulating potassium, calcium, and magnesium homeostasis, as well as water absorption.To achieve these functions, each segment of the tubule has a distinct cellular morphology and expresses unique sets of solute transporters.Finally, the modified filtrate flows into the collecting duct, which in the case of the metanephric kidney, acts as the final regulator of electrolyte balance and water absorption (Hebert et al., 2001).Mouse kidney development begins at E8.5 with the formation of the nephric duct primordium (blue) from the nephrogenic cord (yellow).Rostral nephric duct precursors are lost by apoptosis while caudal cells persist and grow towards the cloaca.As it extends down the trunk the nephric duct induces the formation of mesonephric tubules in the adjacent nephrogenic cord.Only the rostral mesonephric tubules become joined to the nephric duct.At E10.5, an outgrowth called the ureteric bud forms from the nephric duct near the cloaca.The ureteric bud grows into a specialized population of nephrogenic cord cells (red) called the metanephric mesenchyme.Reciprocal inductive interactions between the ureteric bud and the metanephric mesenchyme lead to repeated branching of the ureteric bud and the formation of metanephric nephrons from the metanephric mesenchyme (not shown).

The intermediate mesoderm
The mesoderm, together with the other two embryonic germ layers (ectoderm and endoderm), form during gastrulation.In general, gastrulation is characterized by the movement of an initially multi-potent population of epiblast cells into the interior of the embryo.In mammals, this occurs via the primitive streak, a furrow at the future caudal (posterior) end of the embryo where migrating epiblast cells undergo ingression (Gilbert, 2006).Once these cells have traversed the primitive streak they adopt either a mesodermal or endodermal fate and then become restricted to specific cell types within these lineages.This 'patterning' is best understood in fish and amphibian embryos, where signaling centers on opposite sides of the embryo (dorsal and ventral poles) release secreted factors, such as signaling stembook.orgmolecules like the Bone Morphogenetic Proteins (BMPs) and their antagonists (reviewed by (De Robertis and Kuroda, 2004).It is hypothesized that 'dorsal versus ventral' interactions, as well as positive and negative feedback loops occurring within each signaling center, establish morphogenic gradients across the gastrulating embryo.Particular mesodermal cell fates are thought to be induced, or 'specified', in response to high, medium, or low concentrations of these morphogens.Ultimately, dorsal-ventral patterning results in the mesoderm being subdivided into at least four major populations: (1) notochord (a transient 'embryonic backbone'), (2) paraxial mesoderm (future somites ie progenitors of certain muscles and other connective tissues), (3) intermediate mesoderm (the precursor to the kidneys), and (4) lateral plate mesoderm (includes progenitors of the heart, blood, and vascular cells (see Figure 2).
Perturbations in dorsal or ventral signaling pathways alter the proportions of these mesodermal populations within the embryo.'Dorsalized' embryos have expanded notochord and paraxial mesoderm at the expense of intermediate and lateral plate mesoderm.Whereas 'ventralized' embryos have increased lateral plate and intermediate mesoderm at the expense of paraxial mesoderm and notochord.BMPs are potent ventralizing factors and there is considerable evidence from studies in Xenopus, zebrafish, and chicken to indicate that BMPs act during gastrulation to determine the size and location of the intermediate mesoderm along the medial-lateral axis of the embryo (James and Schultheiss, 2005;Kishimoto et al., 1997;Neave et al., 1997;Nguyen et al., 1998;Xu et al., 1999).BMPs are also needed after gastrulation to induce/maintain the expression of early acting pro-renal genes in the pronephros and to regulate various aspects of metanephric development (Bracken et al., 2008;Obara-Ishihara et al., 1999).

The pronephros and formation of the nephric duct
The mouse pronephros arises from the portion of the intermediate mesoderm that is level with presumptive somites 5-8 at E8.0 (Bouchard et al., 2000;Vetter and Gibley, 1966).In this region, precursors of the pronephric duct separate away from the intermediate mesoderm and form a short longitudinal rod of cells that then grows caudally.These cells undergo a mesenchymal-to-epithelial transition and form the epithelial tube of the pronephric duct (also known as the nephric duct).At the same time, ∼3 small condensations of mesenchymal cells that may represent pronephric nephron precursors arise from the nephrogenic cord.However, these clusters do not differentiate further and pronephros development is aborted (Vetter and Gibley, 1966).The nephric duct degenerates by apoptosis soon after forming but persists in more caudal positions of the trunk where it is required for the formation of the mesonephric and metanephric kidneys (Pietila and Vainio, 2005;Pole et al., 2002).

Molecular regulation of nephric duct formation
Early regulators of nephric duct development include the functionally redundant paired-box homeotic transcription factors Pax2 and Pax8, the zinc finger transcription factor Gata3, and the LIM class homeodomain transcription factor Lhx1 (previously known as Lim1).
Pax2 and Pax8 are co-expressed in nephric duct precursors at E8.5, although neither gene is dependent upon the other for their initial activation (Bouchard et al., 2002;Torres et al., 1995).Pax2 and Pax8 transcripts persist in the nephric duct as it extends caudally (and later in the metanephric collecting duct) and also appear in the nephrogenic mesenchyme of the mesonephros and metanephros where they play a role in nephron formation (see Section 6 below; Kobayashi et al., 2007;Narlis et al., 2007;Plachov et al., 1990;Torres et al., 1995).Pax8 mutants do not display renal defects, whereas in Pax2-deficient mice, the nephric duct forms but does not reach the urogenital sinus and degenerates (Mansouri et al., 1998;Torres et al., 1995).In Pax2/8 double mutants, there are no morphological signs of nephric duct formation and an absence of expression of the nephric duct markers Ret, Lhx1, and Gata3 (Bouchard et al., 2002;Grote et al., 2006).As a result of failed nephric duct formation, no kidney types arise in the double mutants and the intermediate mesoderm undergoes apoptosis at E9.5 (Bouchard et al., 2002).These results indicate that Pax2 and Pax8 act redundantly at an early stage of renal development to commit intermediate mesoderm to the nephric duct lineage.This is not the sole function of Pax2 and Pax8 and other studies have identified additional roles including the formation of mesonephric and metanephric nephrons, UB outgrowth and branching during metanephros development, and anti-apoptotic activities in the metanephric mesenchyme, collecting duct, and nephrons (see Section 6 below for details).
Gata3 is expressed in nephric duct precursors starting at E8.5 and is a putative direct target of Pax2 and Pax8 (Grote et al., 2006).Targeted inactivation of Gata3 causes wayward growth of the nephric duct down the trunk and a loss of Ret expression.This defect leads to reduced mesonephric nephron formation and an absence of the metanephros due to a failure of the nephric duct to complete its extension to the urogenital sinus (Grote et al., 2006).These findings implicate Gata3 as a key regulator of guidance molecules that control nephric duct extension.Although

Mouse kidney development
Ret regulates chemotaxis in some cell types (see below), Ret null embryos do not display defects in nephric duct extension (Schuchardt et al., 1994) therefore other Gata3 targets must exist.
Lhx1 is initially expressed in the intermediate mesoderm and lateral plate mesoderm at E7.5 and E8.5 but becomes restricted to the nephric duct primordium by E9.5 (Barnes et al., 1994;Fujii et al., 1994;Kobayashi et al., 2005;Tsang et al., 2000).Conventional as well as conditional gene targeting approaches have shown that Lhx1 is required for the nephric duct to extend completely down the trunk and fuse with the urogenital sinus.The nephric duct undergoes necrotic degeneration, in Lhx1 mutants possibly contributing to, or causing, the extension defect.Therefore, Lhx1 plays an important role in nephric duct survival.These defects lead to corresponding abnormalities in the formation of the mesonephric and metanephric kidneys with the most severe phenotype being metanephric agenesis (Kobayashi et al., 2005;Pedersen et al., 2005;Shawlot and Behringer, 1995).Direct targets of Lhx1 in the nephric duct are not known and Pax2 expression is not dependent on Lhx1 function (Kobayashi et al., 2005;Pedersen et al., 2005;Tsang et al., 2000).Transcripts for E-cadherin and Wnt9b (implicated in mesonephric and metanephric nephron induction, see below) are reduced in Lhx1 mutants but it is not clear if this is secondary to cell death (Pedersen et al., 2005).Lhx1 is also expressed in nascent nephrons during mesonephric and metanephric kidney development and like Pax2/8, is required at multiple steps of kidney development.

The Mesonephros
The mouse mesonephros consists of up to ∼18 pairs of tubules that extend from the level of somite 10 to 17 and are divided into distinct cranial and caudal sets (Sainio, 2003;Vetter and Gibley, 1966).The nephrons of the cranial set develop rudimentary glomeruli, are frequently branched, and join with the nephric duct at 4-6 sites.Based on the observation that the cranial nephrons appear to be in continuous contact with the nephric duct during their development it has been suggested that the cranial set may form directly from the nephric duct, perhaps as outgrowths (Sainio et al., 1997).However, data from chicken and mouse studies indicate that the duct only contributes cells to a short connecting segment (Brenner-Anantharam et al., 2007;Croisille et al., 1976;Mugford et al., 2008).In contrast, the caudal pairs, which make up the bulk of the mesonephros, are comprised of primitive unbranched tubules that do not connect to the nephric duct and derive from the nephrogenic cord (see Figure 2).These tubules first appear as condensations of nephrogenic cord cells level with somites 8-9 at E9.0 (Vetter and Gibley, 1966).These cells undergo a mesenchymal-to-epithelial transition, initially forming a 'renal vesicle' and then elongating into a 'S-shaped body' (Smith and Mackay, 1991).The mesonephros begins degenerating at E14.5 and within 24 hours almost all of the tubules undergo apoptosis and disappear in a caudal to cranial direction (Sainio et al., 1997;Smith and Mackay, 1991).In females, all of the tubules are lost, whereas in males some of the cranial tubules remain intact, contributing to the epididymal ducts of the testis (Vetter and Gibley, 1966).
The molecular regulation of mouse mesonephros development has received little attention, presumably because of the limited functionality and transient existence of the organ.Classical experiments in chick embryos have demonstrated that microsurgical disruption of nephric duct extension results in a failure of mesonephric nephron formation in the adjacent nephrogenic cord (Boyden, 1927;Waddington, 1938).Thus, it has long been suspected that nephron-inducing signals emanate from the nephric duct as it migrates to the cloaca, resulting in the formation of mesonephric nephrons in a craniocaudal sequence.The gene responsible for nephron induction was recently identified as Wnt9b, encoding a member of the Wnt family of secreted signaling molecules that is expressed by the nephric duct during mouse mesonephric and metanephric development (Carroll et al., 2005).Wnt9b mutants also lack metanephric nephrons (see below), suggesting that similar nephron-inducing programs underlie nephron formation in both mesonephric and metanephric kidneys.In support of this, the transcription factors Pax2, Wilms' tumor suppressor1 (Wt1), Foxc1, and Six1, which are involved in metanephros formation (see below), are also involved in mesonephric nephron formation (Note: Wt1 and Six1 are reported to be only required for the formation of the caudal set of nephrons, however the cranial tubules seen in these mutants may actually represent arrested nephric duct outgrowths; (Kobayashi et al., 2007;Mugford et al., 2008;Sainio et al., 1997;Torres et al., 1995).

The Metanephros
Our understanding of the developmental pathways underlying metanephros formation has advanced significantly over the last two decades.The metanephric mesenchyme expresses a large number of regulatory genes, including the transcriptional regulators Pax2, Wt1, Eya1, Six1, Six2, Osr1, and Hox11.These factors function as regulators of the formation, proliferation, and survival of the metanephric mesenchyme and/or as upstream activators of Gdnf.

Specification of the metanephric mesenchyme
The nephric duct is not required for the initial specification of the metanephric mesenchyme as in the Gata3 knockout mouse, Pax2-expressing metanephric mesenchyme is still found despite failure of the nephric duct to migrate to this region of the embryo (Grote et al., 2006).Early key factors that have been identified as being necessary for the formation of a morphologically distinct region of metanephric mesenchyme are the transcriptional regulators Eya1, Six1/Six4, and Odd1.
6.1.1.Eyes-absent-1 (Eya) and Sine-Oculis (Six) Eya1, a homolog of Drosophila eyes absent, encodes a transcriptional co-activator that can complex with other transcription factors to induce the expression of target genes (Jemc and Rebay, 2007).At E8.5, Eya1 is expressed in the nephrogenic cord caudal to the mesonephros but gets progressively restricted until it is only expressed by the metanephric mesenchyme at E11.5 (Sajithlal et al., 2005).Eya1-deficient embryos do not form a morphologically distinct population of metanephric mesenchyme or a UB at E10.5 (Xu et al., 1999).Eya1 null embryos display an early loss of Gdnf expression in the nephrogenic cord (from E9.5 onwards).This defect is not caused by a failure in the formation of the intermediate mesoderm, as normal expression of Wt1 and Pax2 is observed in the nephrogenic cord at E9.5 (Sajithlal et al., 2005;Xu et al., 1999).At E10.5, transcripts for Pax2 and Six2 are absent in the metanephric region of Eya1 null embryos, suggesting that the metanephric mesenchyme fails to be specified in the mutants.In addition, significant apoptosis in the metanephric region is also observed in the mutants at this stage (Sajithlal et al., 2005;Xu et al., 1999).Although an absence of metanephric mesenchyme marker expression could be secondary to cell loss, a more recent analysis of Eya1 hypomorphic mutants has provided further evidence to support an early role for Eya1 during metanephric mesenchyme differentiation.Eya1 hypomorphs with ∼20% of normal Eya1 protein levels initially develop both the metanephric mesenchyme and a UB, although further UB outgrowth and branching is defective (Sajithlal et al., 2005).Expression of Pax2, Six1, and Gdnf in the metanephric mesenchyme is reduced in the hypomorphs at E10.5, suggesting that Eya1 is required to induce or maintain the expression of these genes.Taken together, these results suggest that Eya1 acts during the early stages of metanephric kidney development to convert nephrogenic cord cells into metanephric mesenchyme, at least in part, by regulating the expression of Pax2, Six1, Six2, and Gdnf.
Eya1 has no apparent DNA-binding activity and is translocated from the cytoplasm to the nucleus by binding to the Six (sine oculis) homeobox transcription factors (Ohto et al., 1999).Candidate Six proteins involved in renal development include Six1, Six2, and Six4, which show overlapping expression patterns in the nephrogenic cord and metanephric mesenchyme (Kobayashi et al., 2007;Li et al., 2003;Oliver et al., 1995;Xu et al., 2003).Functionally, the Six proteins may share similar or redundant activities.Consistent with this, no single knock-out of a Six gene recapitulates the severity of the Eya1 null phenotype.In Six1 null embryos, the metanephric mesenchyme is specified, as determined by morphology and the expression of Wt1 and Eya1, but its size is reduced (Li et al., 2003).Expression of the metanephric mesenchyme markers Sall1, Pax2, and Six2 are severely reduced in the mutants, although differing degrees of down-regulation have been reported (Kobayashi et al., 2007;Li et al., 2003;Sajithlal et al., 2005;Xu et al., 2003).Gdnf is normally expressed in the metanephric mesenchyme of Six1 mutants, although its overall expression domain is smaller given the reduced size of the metanephric mesenchyme (Xu et al., 2003).The UB initially forms at E10.5 in Six1 mutants but often fails to invade the metanephric mesenchyme, perhaps due to a reduced local concentration of Gdnf caused by the smaller mass of metanephric mesenchyme (Yu et al., 2004).As a result, apoptosis of the metanephric mesenchyme ensues at E11.5 and renal agenesis is seen in the majority of Six1-null newborns (Kobayashi et al., 2007;Xu et al., 2003).
Six2 null embryos do not show defects in the initial specification of the metanephric mesenchyme or UB outgrowth, despite expression of Six2 in the metanephric mesenchyme at E10 and the finding that Six2 can activate Gdnf expression (Brodbeck et al., 2004;Self et al., 2006).However, later abnormalities in early nephron formation are found at E11.5 (see below).Six1/Six2 double mutants have not yet been reported.Six4-deficient mice are viable and fertile and exhibit no major developmental defects (Ozaki et al., 2001).A recent analysis of Six1/Six4-deficient embryos has demonstrated clear functional redundancy between the Six1 and Six4 proteins with loss of both genes leading to a more severe metanephric phenotype than that of Six1-deficient mutants (Kobayashi et al., 2007).A morphologically distinct region of metanephric mesenchyme is missing in Six1/Six4 double mutants and there is an absence of Pax2, Sall1, and Gdnf expression in the metanephric region.In addition, Pax8, which functions redundantly with Pax2 (see above), is transiently expressed in the metanephric mesenchyme at E10.0 and while it is normally expressed in Six1-deficient embryos, it is absent in the Six1/Six4 double mutants.Nephrogenic cells appear to still be present in the Six1/Six4 mutants based on the expression of Wt1, Six1, and Osr1 (Kobayashi et al., 2007).No apoptosis in the metanephric region was observed at E10.5, although it presumably occurs at least as early as E11.5 based on the Six1 phenotype (see above).The UB fails to form in Six1/Six4 mutants and renal agenesis is seen in all of the newborns.

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Overall, the phenotype of Six1/Six4 mutants is similar to that of Eya1 mutants, strongly suggesting that Six1 and Six4 interact redundantly with Eya1 to activate expression of metanephric regulators such as Pax2/8, Six2, Sall1, and Gdnf.Whether Eya1/Six complexes directly activate the expression of these genes is not clear, although chromatin immunoprecipitation experiments have shown that Eya1 and Six1 are present on Gdnf regulatory sequences (Li et al., 2003).
Eya1 can interact with other transcription factors and a recent study has implicated an Eya1-Pax2-Hox11 complex as a direct activator of Six2 as well as Gdnf (Gong et al., 2007;Mugford et al., 2008).Consistent with this, targeted inactivation of all three Hox11 paralogs causes a significant reduction in Six2 and Gdnf expression in the metanephric mesenchyme at E10.5 (Wellik et al., 2002).However, expression of Pax2 is normal in Hox11 triple mutants whereas it is absent in Six1/Six4 double mutants, suggesting that a Hox11-Eya1-Pax2 complex may act later in development, perhaps after an Eya1/Six1/4 complex has upregulated Pax2 and Sall1 in the metanephric mesenchyme (see Figure 4).The ability of Eya1 to interact in multiple complexes and to induce the expression of genes encoding transcription factors it physically associates with, make it difficult to place Eya1 in a simple linear pathway.

Odd-skipped related-1
Odd-skipped related-1 (Odd1) encodes a zinc-finger transcription factor related to the Drosophila pair rule gene odd skipped (Coulter et al., 1990).Odd1 is one of the earliest molecular markers of the intermediate mesoderm in the mouse embryo and is first activated in these cells shortly after they migrate from the primitive streak at the midgastrula stage (Wang et al., 2005).At E8.5-9.5, Odd1 transcripts are found throughout the intermediate mesoderm/nephrogenic cord and in the metanephric mesenchyme but not the UB at E10.5 (James et al., 2006;So and Danielian, 1999;Wang et al., 2005).In Odd1 null embryos, neither the UB nor a morphologically distinct population of metanephric mesenchyme can be detected and renal agenesis occurs in mutants that survive to late gestation (Wang et al., 2005).Consistent with this, Odd1 mutants completely lack Eya1 and Pax2 in the metanephric region at E9.5 (James et al., 2006).Wt1 expression levels are reduced in the Odd1 mutants, but Wt1 protein can still be detected in the metanephric region.High levels of apoptosis are evident in the mutant metanephric mesenchyme at E10.5, consistent with the downregulation of Eya1 (see above; James et al., 2006;Wang et al., 2005).At E11.5, transcripts for Six2, Gdnf, and Sall1 cannot be detected, also possibly due to the absence of Eya1, however cell loss by apoptosis may contribute to the failure to detect markers of the metanephric mesenchyme.Odd1 mutants also display nephric duct defects that are characterized by discontinuous expression of Ret, Lhx1, Pax2, posterior truncations, and a smaller nephric duct diameter (James et al., 2006;Wang et al., 2005).The cause of these abnormalities has not been examined but may be due to increased nephric duct cell death, perhaps indirectly resulting from the loss of the adjacent nephrogenic cord (given that Odd1 transcripts are not found in the migrating nephric duct; James et al., 2006).Interestingly, the duct defects are more severe on the left side of the embryo, suggesting that pathways that establish left-right patterning may interact with Odd1 (Wang et al., 2005).
The direct targets of Odd1 during kidney development are not known and current evidence indicates that Odd family members act as transcriptional repressors (Goldstein et al., 2005;Tena et al., 2007).Thus, the effects of Odd1 on renal genes such as Eya1 and Pax2 may be mediated indirectly via the inhibition of a repressor of these genes.Taken together, these findings place Odd1 as one of the earliest acting genes involved in metanephros formation and suggest that Odd1 acts upstream Eya1, Pax2, and Wt1 in the nephrogenic cord to promote metanephric mesenchyme formation and survival (see Figure 4 and Figure 5).

Paired-box transcription factor (Pax) 2 and Pax8
Pax2 is expressed in the nephrogenic cord in the metanephric region at E9.5 and then in the metanephric mesenchyme at E10.0.Transcripts for Pax2 are also found in the nephric duct (as described above) and in the UB as it invades the metanephric mesenchyme (Brophy et al., 2001;Torres et al., 1995).In Pax2 mutants, the nephric duct does not reach the cloaca, expression of Ret is lost, and the duct starts degenerating by E12.5.As a result, the UB never forms and metanephric development does not occur (Torres et al., 1995).The metanephric mesenchyme can be morphologically distinguished in Pax2 mutants and expresses Eya1, Six1, Six2 (albeit weakly) and Sall1, indicating that Pax2 is not required for the initial specification of the metanephric mesenchyme from the nephrogenic cord (Torres et al., 1995;Xu et al., 2003).However, the transient expression of Pax8 in the metanephric mesenchyme at E10.0 may mask an earlier role for Pax2 and Pax8 in the formation of the metanephric mesenchyme (Kobayashi et al., 2007).Transcripts for Gdnf

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Mouse kidney development are reduced in the Pax2-deficient metanephric mesenchyme, consistent with Pax2 participating in a transcriptional complex with Eya1 and Hox11 proteins on Gdnf regulatory sequences (see above; (Sajithlal et al., 2005).

Glial-derived neurotrophic factor
Gdnf is expressed broadly throughout the nephrogenic cord at E9.5 but becomes restricted to the region of the metanephric mesenchyme by E10.5 (Grieshammer et al., 2004;Hellmich et al., 1996;Pichel et al., 1996;Sanchez et al., 1996).GDNF signals through the Ret tyrosine kinase receptor, which is expressed by the nephric duct, together with a membrane-tethered GFRa1 co-receptor (Baloh et al., 1997;Pachnis et al., 1993;Sainio et al., 1997).GDNF signaling also requires cell surface heparan sulphate glycosaminoglycans that bind to GDNF and may play a role in ligand presentation to the receptor (Bullock et al., 1998;Davies et al., 2003;Rider, 2003;Tanaka et al., 2002).GDNF binding to the Ret receptor leads to activation of the phosphatidyl inositol 3-kinase and extracellular signal-related kinase (ERK) signaling pathways and promotes chemotaxis and proliferation in a range of cells (Fisher et al., 2001;Hu et al., 1999;Natarajan et al., 2002;Tang et al., 2002;Tang et al., 1998;Watanabe and Costantini, 2004;Young et al., 2001).The majority of mouse embryos deficient in Gdnf, Ret, or Gfra1 fail to form a UB, although the observation that a UB forms in a fraction of the mutants indicates that additional UB inducing signals must also exist (Cacalano et al., 1998;Maeshima et al., 2007;Moore et al., 1996;Pichel et al., 1996;Sanchez et al., 1996).
Various studies using GDNF-soaked beads and transgenic overexpression of Gdnf have demonstrated the importance of localizing GDNF-Ret signaling so as to prevent the formation of ectopic UBs (Brophy et al., 2001;Sainio et al., 1997).The maintenance and/or activation of Gdnf expression in the metanephric mesenchyme are dependent upon a host of regulatory factors including transcription factors (Eya1, Six1, Sall1, Pax2, Hox11 proteins), secreted factors (Gdf11, Nephronectin) and FGF signaling (see above and below for details).Inhibitors of Gdnf expression include Foxc1, a forkhead transcription factor, and the Robo2/Slit2 receptor/ligand pair best known for their chemorepellent role during neuron and axon migration (Andrews et al., 2007).In embryos deficient in Foxc1 there is an abnormal maintenance of Gdnf (and Eya1) in more anterior portions of the nephrogenic cord and a corresponding induction of ectopic UB from portions of the nephric duct just anterior to the normal site of UB formation (Kume et al., 2000).Similar phenotypes of expanded Gdnf expression and supernumerary UBs are seen in Slit2 and Robo2 mutants (Grieshammer et al., 2004).Slit2 is expressed in the nephric duct and weakly in the metanephric mesenchyme, with higher levels in the nephrogenic cord anterior the Gdnf expression domain.Robo2 is highly expressed in the nephrogenic cord but weakly in the region of the nephric duct where the UB forms.Thus, the expression patterns of Slit2 and Robo2 are consistent with either a role in restricting Gdnf expression or possibly a more general role in restricting the size of the metanephric mesenchyme.The downstream targets of Slit2-Robo2 signaling in the nephrogenic cord are unknown but do not appear to be mediated via alterations in the expression domains of Foxc1 or Eya1 (Grieshammer et al., 2004).

Fibroblast growth factors
The first indication that signaling via the FGF receptors (FGFRs) was important for early metanephric development came from the study of a transgenic line that expressed a secreted dominant negative FGF receptor that could inhibit multiple FGFs (Celli et al., 1998).Half of the mutant transgenic embryos at E18.5 displayed renal agenesis or small malformed kidneys.A more definitive requirement of FGF signaling for UB outgrowth came from the conditional inactivation of Fgfr1 and Fgfr2 (Poladia et al., 2006).These FGF receptors are expressed in both the metanephric mesenchyme and UB at E10.5 and E11.5.While single deletion of Fgfr1 or Fgfr2 from the metanephric mesenchyme does not result in any kidney abnormalities, loss of both receptors causes renal agenesis (Poladia et al., 2006).The UB initially forms normally in the double mutants at E10.5 but it does not elongate further or branch and undergoes apoptosis by E11.5.Interestingly, Fgfr1/2 mutants occasionally develop two UBs, suggesting that FGF signaling in the metanephric mesenchyme is also needed to prevent ectopic UB outgrowth.The metanephric mesenchyme is greatly reduced in Fgfr1/2 mutants and appears hypo-proliferative and apoptotic at E10.5.Despite this, Gdnf is still expressed at this stage, consistent with the initial formation of the UB in the mutants.Subsequently, Gdnf levels are lost at E11.5 suggesting that a failure to maintain Gdnf expression is the underlying cause for the arrested UB outgrowth phenotype.The Fgfr1/2 deficient metanephric mesenchyme, albeit reduced in size, expresses Eya1, Six1, and Wt1 at E10.5.However, transcripts for Pax2, Six2, and Sall1 are absent in the mutants at this stage, indicating that FGF signaling lies upstream of these transcription factors.The FGF ligand/s responsible for activating FGFR1 or FGFR2 in the metanephric mesenchyme are not known and no single Fgf knockout has recapitulated the Fgfr1/r2-deficient renal phenotype, presumably due to redundancy.

Sall1
The Sall gene family in mammals includes four members (Sall1-4) that encode homologues of the Drosophila homeotic gene Spalt, a multi-zinc finger transcription factor that acts as both a repressor and an activator (Nishinakamura and Osafune, 2006).Of these Sall1 plays a clear role in the development of the metanephros.Transcripts for Sall1 are found in the metanephric mesenchyme at E10.5, prior to UB formation.In Sall1-null embryos, the metanephric mesenchyme can be morphologically distinguished, although it is reduced in size, and expresses a number of molecular markers such as Pax2, WT1, and Eya1.The UB forms in Sall1-deficient embryos but it does not complete its outgrowth into the metanephric mesenchyme and renal agenesis occurs in a high percentage of the newborns (Nishinakamura et al., 2001).As with other mutants that show failed UB invasion, expression of Gdnf is initially normal in Sall1 mutants at E10.5 but is lost by E11.5.Similarly, increased apoptosis of the metanephric mesenchyme, a hallmark of failed UB outgrowth, is evident in Sall1 mutants at E11.5.Sall1/Sall4 compound heterozygotes have also been reported to display a renal agenesis phenotype, however the expression pattern of Sall4 in the metanephros has not been described and the details of this genetic interaction are unclear (Sakaki-Yumoto et al., 2006).
Expression of Sall1 is absent in Six1 mutants suggesting that Sall1 may be a target of an Eya1-Six1-containing transcriptional complex (see Figure 4).Consistent with this, analysis of the human SALL1 promoter identified Six1 binding sites and demonstrated synergistic activation of the promoter in vitro following Six1 and Eya1 transfection (Chai et al., 2006).Sall1 and Six1 mutants have common renal defects including reduced size of the metanephric mesenchyme and failed UB invasion (Li et al., 2003;Xu et al., 2003).Sall1 expression is also lost in Fgfr1/2 conditional mutants (see above), indicating that both FGF signaling and an Eya1-Six1 complex is necessary for Sall1 expression in the metanephric mesenchyme.

Growth/differentiation factor 11
A loss of Gdnf expression in the metanephric mesenchyme is seen at E11.5 in mutants defective in Growth/differentiation factor 11 (Gdf11), encoding a member of the TGF-β/BMP superfamily.Gdf11 is expressed in the nephric duct, UB, and the metanephric mesenchyme at E10.5 (Esquela and Lee, 2003).The majority of Gdf11 mutants show bilateral renal agenesis resulting from an absence of UB outgrowth, presumably due to the loss of Gdnf expression in the metanephric mesenchyme.Thus, GDF11 is implicated as an upstream inducer of Gdnf expression.However, earlier stages were not examined in the Gdf11 mutants and it is not known if Gdnf is initially expressed at E10.5 but then is not maintained in the metanephric mesenchyme at later stages.Maintenance of Gdnf expression in the metanephric mesenchyme after E10.5 depends upon UB invasion of the metanephric mesenchyme and most likely the establishment of a GDNF-Ret positive feedback loop (see below).Therefore, the reduced expression of Gdnf in Gdf11 mutants could be a secondary consequence of failed UB invasion.
GDF11 can signal via complexes of the Activin type 2b receptor (Acvr2b) and the ALK5 type 1 receptor, and consistent with this, renal agenesis is seen in Alk5 +/− ; Acvr2b −/− mutants (Andersson et al., 2006).GDF11 signaling via Alk5/Acvr2b has also been implicated in anterior-posterior patterning of the embryonic axis (upstream of the Hox genes) and the hindlimbs and metanephric mesenchyme are posteriorly displaced in the mutants (Andersson et al., 2006;McPherron et al., 1999).Whether axial patterning abnormalities are involved in the UB outgrowth defect is not known but the metanephric mesenchyme appears to form normally based on its morphological appearance, expression of markers such Eya1 and Pax2, and its ability to undergo nephrogenesis in vitro (Esquela and Lee, 2003).The nephric duct from Gdf11 mutants can be induced in culture to form UB outgrowths in response to exogenous GDNF, consistent with the notion that the primary defect is a loss of Gdnf expression in the metanephric mesenchyme.Interestingly, in these experiments it was found that the Gdf11 mutant nephric duct is hypersensitive to GDNF, thus raising the possibility that GDF11 may function to antagonize inhibitors of UB outgrowth (see below).

Nephronectin and α8β1 integrin
Gdnf expression in the metanephric mesenchyme is transiently dependent on the extracellular matrix (ECM) protein Nephronectin (Npnt) and the cell adhesion receptor subunit α8 integrin (Itga8; Brandenberger et al., 2001;Linton et al., 2007).The α8 integrin subunit forms a dimeric cell surface receptor complex with β1 integrin (α8β1) and binds a number of ECM proteins including Nephronectin.Transcripts for Itga8 are found throughout the nephrogenic cord as well as the metanephric mesenchyme, while Npnt is expressed by the UB (Brandenberger et al., 2001;Muller et al., 1997).The renal phenotypes of Npnt and Itga8 null mutants are very similar; the UB initially forms but its invasion into the adjacent metanephric mesenchyme is delayed (Linton et al., 2007;Muller et al., 1997).Although some recovery in UB growth and branching subsequently occurs, this is not sufficient to prevent a high frequency of kidney agenesis stembook.orgoccurring in the newborn mutants.This defect is correlated with a transient down-regulation of Gdnf transcripts in the metanephric mesenchyme at E11.5, followed by restored expression at E13.5, and normal levels of Gdnf regulators such as Eya1, Pax2, Six2, and Gdf11 (Linton et al., 2007).The penetrance of the Itga8 mutant kidney phenotype can be made more or less severe by genetically modulating the level of GDNF-Ret signaling in vivo, supporting the hypothesis that a transient reduction in Gdnf expression underlies the cause of the kidney agenesis phenotype (Linton et al., 2007).

Wilms' Tumor Suppressor-1
The Wilms' tumor suppressor-1 gene (Wt1) encodes a zinc finger transcription factor and mRNA splicing co-factor.WT1 is considered a potential regulator of GDNF signaling, although the details of how WT1 interacts with the GDNF pathway remain obscure.Wt1 is initially expressed throughout the nephrogenic cord as early as E9.0 and is maintained weakly in the metanephric mesenchyme prior to UB outgrowth at E10.5 (Armstrong et al., 1993;Pellegrini et al., 1997).The UB fails to form in Wt1 null mutants and the metanephric mesenchyme, which appears morphologically normal and expresses Pax2 and Six2, undergoes apoptosis at E11.5 and is lost by E12.0 (Donovan et al., 1999;Kreidberg et al., 1993).Although this phenotype resembles loss of GDNF signaling, transcripts for Gdnf are still detectable in the metanephric mesenchyme of Wt1 mutant embryos (Donovan et al., 1999).This finding led to the suggestion that GDNF protein levels may be reduced or absent in Wt1 mutants or alternatively Wt1 may be needed to boost Gdnf expression levels above a critical threshold needed for UB outgrowth (Donovan et al., 1999;Gao et al., 2005).A more recent study suggests that Wt1 may act upstream of vascular endothelial growth factor-a (Vegfa) to stimulate angioblasts to release an, as-of-yet unidentified, factor that induces Pax2 and Gdnf expression.WT1 is likely to play multiple roles during metanephros development as classic tissue recombinant experiments have also shown that Wt1 mutant metanephric mesenchyme can not be induced to undergo nephrogenesis (Donovan et al., 1999;Kreidberg et al., 1993).

Sprouty1
Supernumerary UB buds that are not associated with alterations in the Gdnf expression domain are seen in embryos deficient in Sprouty1 (Spry1; Basson et al., 2005).Sprouty genes encode cytoplasmic membrane-associated inhibitors of receptor tyrosine kinase signaling (Mason et al., 2006).Spry1 is expressed in both the nephric duct and the metanephric mesenchyme, however, conditional inactivation of Spry1 in the nephric duct results in a similar phenotype to the conventional null mutant (Basson et al., 2005).Therefore, Spry1 function is required in the nephric duct to prevent ectopic UB formation, most likely by preventing excessive GDNF-Ret signaling.In support of this role, reducing the level of GDNF in Spry1 null embryos by inactivating one Gdnf allele rescued the kidney defects in 75% of the compound mutants.Expression of Spry1 in the nephric duct was upregulated in response to GDNF-soaked beads and reduced in Ret mutant embryos, consistent with the observation that Sprouty genes are often upregulated by the same pathways that they inhibit (Basson et al., 2005;Mason et al., 2006).Based on these findings, Spry1 likely forms part of a GDNF-Ret negative feedback loop that lowers the sensitivity of the nephric duct to GDNF and helps ensure that only a single UB is induced during metanephros development (see Figure 5).

Bone morphogenetic protein 4 and gremlin1
BMP4 has also been implicated as a negative regulator of UB outgrowth.BMP4 is expressed in stromal cells enveloping the nephric duct prior to the outgrowth of the UB (Dudley and Robertson, 1997).Although Bmp4 null embryos die during early development, heterozygotes frequently display an ectopic UB (Miyazaki et al., 2000;Miyazaki et al., 2003;Winnier et al., 1995).Organ culture studies have revealed that BMP4 can block the ability of GDNF to induce ectopic budding from the nephric duct (Brophy et al., 2001).BMP4 activity can be inhibited following binding to the secreted BMP antagonist encoded by Gremlin1 (Grem1), which is expressed in an overlapping expression domain with Bmp4 during the early stages of UB outgrowth (Hsu et al., 1998;Michos et al., 2007;Michos et al., 2004).Grem1-deficient embryos show arrested UB outgrowth and the majority of animals are born without metanephric kidneys.These defects are rescued following inactivation of one copy of the Bmp4 gene, consistent with the Grem1 null phenotype being caused by excessive BMP4 signaling (Michos et al., 2007;Michos et al., 2004).Expression of Gdnf in the Grem1 mutant metanephric mesenchyme is initially normal but is downregulated progressively and lost by E11.75.While these observations suggest that locally inhibiting BMP4 signaling around the nascent UB is needed to maintain Gdnf expression, treatment of isolated metanephric mesenchyme with either BMP4 or Grem1 does not alter Gdnf expression.An elevated number of cells positive for phosphorylated Smad1/5/8 proteins, which mediate canonical BMP signaling, were found in the metanephric mesenchyme of Grem1 mutants (Michos et al., 2007).However, the importance of this is unclear as inactivation of Smad4, encoding the common Smad co-factor, in

stembook.org
Mouse kidney development the metanephric mesenchyme does not affect UB outgrowth (Oxburgh et al., 2004).Thus, the mechanism-of-action by which BMP4 inhibits UB outgrowth and whether the nephric duct or metanephric mesenchyme is the target tissue that responds to BMP4 remain unclear.

Survival, proliferation, and condensation of the metanephric mesenchyme
The UB invades the metanephric blastema at E11 and induces the condensation of a subset of metanephric mesenchyme cells around the duct tip.These cells, known as 'induced mesenchyme' or 'cap mesenchyme', form a layer 4-5 cells thick that are morphologically distinguishable from the more peripheral 'uninduced' mesenchyme.Cap mesenchyme cells express a range of transcription factors, including Pax2, Eya1, Six2, Wt1, Sall1, many of which are initially activated in the metanephric mesenchyme, as well as secreted molecules such as GDNF and BMP7 (see Figure 5).The cap mesenchyme is essential for inducing UB branching as well as providing a source of progenitor cells that differentiate into nephrons (see below).Therefore, the formation and preservation of these cells is critical for metanephros formation.
At least three signals are needed to induce and maintain the cap mesenchyme.First, a survival signal must prevent the metanephric mesenchyme from executing a default apoptotic pathway (Coles et al., 1993;Grobstein, 1955;Koseki, 1993;Weller et al., 1991).Failure to induce survival of the metanephric mesenchyme results in programmed cell death and kidney agenesis.This phenotype is seen in mutants that fail to form a UB outgrowth or when the metanephric mesenchyme is physically separated from the UB in vitro (Koseki et al., 1992).Second, the cap mesenchyme must be induced to proliferate in order to ensure that new UB tips acquire a sufficient number of cells to maintain subsequent rounds of branching and nephron formation.In this regard, the cap mesenchyme is considered to represent a pool of self-renewing progenitor cells.A recent fate mapping study has shown that Six2-expressing cap mesenchyme cells display a tremendous capacity for expansion and are able to increase their number by 15-fold in 8 days (Kobayashi et al., 2008).Third, a signal promotes the condensation/recruitment of metanephric mesenchyme around the UB tip.This signal is poorly understood but appears to depend on Smad4, encoding an intracellular mediator of TGFβ/BMP signaling, as conditional inactivation of Smad4 in the metanephric mesenchyme results in the cap mesenchyme failing to efficiently coalesce around the UB tips (Oxburgh et al., 2004).The transcriptional regulation of survival, anti-apoptotic, and condensation factors in the UB is not well understood but may be downstream of the Emx2 homeobox transcription factor that is expressed by the UB.Emx2 mutant embryos show normal UB outgrowth but the metanephric mesenchyme fails to proliferate or condense around the UB tips followed by the degeneration of the metanephric mesenchyme and UB by E13 (Miyamoto et al., 1997).
Members of the Wnt, FGF, and BMP families of secreted factors, as well as Pax2 and Pax8, have been implicated as anti-apoptotic and/or pro-growth factors for the metanephric mesenchyme, and likely act in a partially redundant fashion (Barasch et al., 1997;Dudley et al., 1999;Dudley and Robertson, 1997;Grieshammer et al., 2005;Luo et al., 1995;Narlis et al., 2007;Oxburgh et al., 2005;Perantoni et al., 1995;Poladia et al., 2006;Schmidt-Ott et al., 2007).There is a clear in vivo requirement for BMP7 to function as an anti-apoptotic factor for the metanephric mesenchyme.Bmp7 is expressed in the UB and cap mesenchyme and while the initial stages of UB outgrowth and branching occur normally in Bmp7 mutants, the metanephric mesenchyme starts undergoing apoptosis at E13.5 and is lost by E16.5 (Dudley et al., 1999;Dudley and Robertson, 1997;Luo et al., 1995;Lyons et al., 1995).As a result, Bmp7 deficient embryos exhibit a depletion of the cap mesenchyme, premature termination of kidney development, and reduced UB branching.Explant experiments further support a role for BMP7 as a survival factor for the cap mesenchyme and also suggest that it may help maintain these cells in an undifferentiated state (Dudley et al., 1999)).These effects are probably shared by other Bmps expressed in the kidney, such as Bmp2 and Bmp4, as a gene 'knock-in' approach demonstrated that Bmp4 could fully substitute for Bmp7 (Oxburgh et al., 2005).

Glial-derived neurotrophic factor (GDNF)
In addition to promoting UB outgrowth, GDNF-Ret signaling also plays a central role in subsequent UB branching, probably by stimulating the cell migration and proliferation that characterizes the UB tip (Costantini and Shakya, 2006).Following UB invasion of the metanephric mesenchyme, Gdnf becomes expressed in the cap mesenchyme surrounding each UB tip (Hellmich et al., 1996;Sainio et al., 1997).This restricted expression pattern is not essential for GDNF function, as transgenic expression of Gdnf throughout the ureteric epithelium of Gdnf-null mutants does not significantly alter UB branching (Shakya et al., 2005).Expression of Ret becomes localized to the UB tips and maintenance of this expression pattern is dependent upon retinoic acid signaling, consistent with earlier observations linking vitamin A/retinol deficiency with renal malformations (Batourina et al., 2001;Mendelsohn et al., 1999;Wilson and Warkany, 1948).Based on the expression of retinoic acid receptors, retinoic acid is not thought to signal directly to the UB but is instead hypothesized to stimulate the release of an unknown Ret-inducing factor from surrounding stromal cells (Batourina et al., 2001;Dolle et al., 1990;Mendelsohn et al., 1999).Whether this factor stimulates Ret expression in the UB or acts via the metanephric mesenchyme is not known.The localization of Ret to the UB tip is important for branching morphogenesis as misexpression of c-ret throughout the ureteric epithelia has been shown to inhibit UB growth and branching in transgenic mice, possibly by acting as a 'sink' for GDNF (Srinivas et al., 1999).
Ret is a downstream target of GDNF signaling and forms part of a positive feedback loop (see Figure 5).Another component of this auto-regulatory loop is Wnt11, which is dependent upon GDNF signaling for its UB tip-specific expression pattern and which contributes to the maintenance of Gdnf expression in the adjacent cap mesenchyme (Kispert et al., 1996;Majumdar et al., 2003;Pepicelli et al., 1997).However, the branching defect in Wnt11 mutant embryos is relatively mild, most likely because Gdnf expression levels are only slightly reduced.Expression of Wnt11 is downregulated in the UB tips of Pax2/Pax8 compound heterozygotes, which also show a reduced UB branching phenotype, suggesting that the stimulatory effects of GDNF on Wnt11 may be mediated via the Pax2/8 transcription factors (Narlis et al., 2007).Wnt11 can signal via the non-canonical planar cell polarity pathway, which has been implicated as a modulator of cell shape and migration, therefore, in addition to participating in a GDNF positive feedback loop, Wnt11 may also act in a pathway parallel to the GDNF-Ret axis (Tada et al., 2002).
Sprouty1 also plays a role in regulating UB branching in response to GDNF-Ret signaling.Spry1 is expressed in the ureteric tree and at a much lower level in the cap mesenchyme.In conventional Spry1 mutants and in conditional mutants lacking Spry1 in the UB-derived epithelium, the UB displays increased budding/branching with significantly larger ureteric trunks and dilated UB tips (Basson et al., 2006).These defects were associated with ectopic expression of Wnt11 in the connecting segments and increased expression of Gdnf in the cap mesenchyme.These results are consistent with the ureteric epithelium in Spry1 mutants being hypersensitive to GDNF, leading to ectopic Wnt11 expression, and a corresponding upregulation of Gdnf in the mesenchyme.The increased level of GDNF-Ret signaling at the UB tip is then hypothesized to be the primary cause of the observed branching defects in Spry1 mutants.

Wnts
Wnt signaling via the canonical β-catenin pathway has been implicated in UB branching (Bridgewater et al., 2008;Maretto et al., 2003;Moriyama et al., 2007).Studies with transgenic reporter mice have demonstrated that βcatenin-induced genes are active in the UB during branching morphogenesis (Maretto et al., 2003;Moriyama et al., 2007).UB-specific inactivation of β-catenin arrests branching at E12.5 resulting in renal aplasia or renal dysplasia (Bridgewater et al., 2008).In addition, this phenotype is associated with reduced expression of Gdnf and Ret in the cap mesenchyme and UB tip, respectively.A number of Wnts capable of signaling through the canonical β-catenin pathway are expressed in the developing metanephros, including Wnt6, Wnt7b, and Wnt9b in the collecting duct system, and Wnt4 in early nephron precursors (Merkel et al., 2007).Of these, loss of Wnt4 or Wnt9b leads to a disruption in UB branching after the T-stage, with the Wnt9b mutant phenotype being more severe than the Wnt4 mutant phenotype (Carroll et al., 2005;Stark et al., 1994).The observation that a branching defect occurs following loss of Wnt4, which is expressed in the renal vesicle below the UB tip, suggests a feedback mechanism in which nephrons induced in response to branching use Wnt4 to promote further UB branching (see Figure 5).In Wnt9b mutant embryos, expression of Wnt11 and Gdnf is downregulated prior to the morphological appearance of the branching defect (Carroll et al., 2005).However, given the reciprocal nature of interactions occurring between the cap mesenchyme and the UB tip and the existence of a GDNF-Ret auto-regulatory loop, it is not known if the cellular target of Wnt9b activity is the cap mesenchyme or the UB.
The identities of the genes regulated by Wnt signaling in the UB are still being elucidated.An analysis of kidneys deficient in β-catenin in the UB has identified Emx2 as a possible early Wnt target (Bridgewater et al., 2008).In addition to the metanephric mesenchyme survival phenotype mentioned above, Emx2 mutants exhibit decreased expression of Lhx1 and Ret in the UB (Miyamoto et al., 1997).UB-specific deletion of Lhx1 also causes reduced Ret expression and reduced UB branching, leading to the hypothesis that a β-catenin-Emx2-Lhx1-Ret pathway may be involved in maintaining Ret expression during UB branching (Bridgewater et al., 2008;Kobayashi et al., 2005).

Fibroblast growth factors
In vitro studies have demonstrated that transient addition of multiple FGFs to kidney organ cultures increases UB growth and branching (Qiao et al., 2001;Qiao et al., 1999).Corroborating in vivo evidence that FGFs participate in UB stembook.orgbranching comes from the genetic manipulation of Fgfr2.UB-specific deletion of Fgfr2 results in small metanephroi with long, thin ureteric trunks and fewer UB tips (Zhao et al., 2004).Similar, but less severe, growth and branching phenotypes are seen in mutants singly deficient in Fgf7, Fgf10, and Fgfr2IIIb (the main receptor isoform for FGF7 and FGF10 (Ohuchi et al., 2000;Qiao et al., 1999;Revest et al., 2001).

Bone Morphogenetic Proteins
BMP signaling plays a role in UB branching.Transcripts for the closely related genes Bmp2 and Bmp4 are found in the mesenchyme surrounding the tips of the branching UB and stromal cells surrounding the nephric duct and the stalk of the UB outgrowth (future ureter), respectively (Dudley and Robertson, 1997).Organ culture experiments have shown that BMP4 can inhibit UB branching directly and at least part of this effect is due to an antagonism of GDNF signaling (Brophy et al., 2001;Bush et al., 2004;Cain and Bertram, 2006;Martinez et al., 2002;Miyazaki et al., 2000;Raatikainen-Ahokas et al., 2000).UB-specific expression of a constitutively active Alk3 transgene, encoding the BMP receptor type IA, results in decreased branching (Hu et al., 2003).UB-specific loss of Alk3 causes a biphasic branching defect that is characterized by an early increase in branching followed by a decrease that results in an overall reduction in UB tip number (Hartwig et al., 2008).These findings suggest that ALK3 signaling normally functions to limit UB branching during early stages of branching morphogenesis.The later branching defect caused by Alk3 deficiency is postulated to be secondary to the early abnormal branching pattern.No alterations in the rates of cell proliferation or apoptosis were found in the Alk3 mutants and nor were there any qualitative differences in the expression levels of Gdnf, Ret, Wnt11 at E11.5 compared to wild-type kidneys (Hartwig et al., 2008).Thus, the downstream targets mediating the effects of Alk3 signaling on UB branching are unclear.Surprisingly, UB-specific deletion of Smad4 has no effect on UB branching, indicating that BMPs must exert their effects via a Smad4-independent pathway (Oxburgh et al., 2004).

Stromal cells
In addition to the UB and the cap mesenchyme, renal stromal cells have been identified as an important source of metanephric regulatory signals, such as the production of retinoic acid as described above.Traditionally, these cells been assumed to arise from the uninduced metanephric mesenchyme but more recent evidence suggests that they may derive from cells surrounding the metanephric mesenchyme (Cullen-McEwen et al., 2005).By E14, stromal cells can be seen in three major layers: the capsular stroma, consisting of a single continuous layer of flattened cells at the outside edge of the kidney, cortical stroma, surrounding the cap mesenchyme and UB tips towards the periphery, and the medullary stroma (Cullen-McEwen et al., 2005).
Cortical and capsular stromal cells express the Foxd1 transcription factor and inactivation of this gene reduces UB branching and causes disorganized and delayed nephron formation (Hatini et al., 1996;Levinson et al., 2005).Associated with this phenotype is an expansion of the cap mesenchyme, suggesting that the stroma plays an important role in controlling the rate of cap mesenchyme differentiation and/or self-renewal.A more recent analysis of Foxd1 mutants has revealed that the maturation of the kidney capsule is abnormal and instead of forming a single homogenous layer of cells, a thicker layer that fails to express capsule markers is formed.Included in the mutant capsule are ectopic Bmp4-expressing cells that are hypothesized to inappropriately signal to the cap mesenchyme and UB tips leading to delayed and disorganized nephron formation and reduced UB branching (Levinson et al., 2005).These findings highlight the importance of the stromal cells in establishing a signaling environment that is conducive to normal metanephric growth and development.
Cap mesenchyme and branching defects similar to that seen in Foxd1 mutants are also seen in embryos defective in the Pbx1 and Pod1 transcription factors, however the epistatic relationships between these genes and Foxd1 is not clear (Quaggin et al., 1999;Schnabel et al., 2003).

Metanephric nephron development
Nephron formation begins at E11.5 with the appearance of small clusters of mesenchymal cells on either side of the unbranched UB tip.These pre-tubular aggregates initially consist of 4-6 cells that are contiguous with the cap mesenchyme but undergo rapid proliferation to form a cluster of approximately 30 cells (Bard et al., 2001).Lineage labeling experiments both in vitro and in vivo have confirmed that the cap mesenchyme gives rise to all of the epithelial segments of the nephron (podocytes through to the distal tubule; Boyle et al., 2008;Herzlinger et al., 1992;Kobayashi et al., 2008;Osafune et al., 2006).Following UB branching and growth, the pre-tubular aggregates become located beneath the UB tips (known as the proximal side).Similar to the morphogenesis seen for mesonephric nephrons, the pre-tubular aggregates undergo a mesenchymal-to-epithelial transition to form renal vesicles at E12.5 and then proliferate to give rise to comma-and S-shaped bodies that fuse with the collecting duct epithelium (see Figure 6).
Based on restricted gene expression patterns, the S-shaped body can be subdivided into podocyte progenitors and the precursors of the proximal and distal tubule segments, although definitive lineage labeling experiments have not yet been done (Dressler, 2006).The cells that make up the cleft at the proximal end of the S-shaped body (farthest away from the collecting duct) express Wt1 and mature into podocytes.These cells also produce VEGF and attract angioblasts that contribute to the formation of the glomerulus (Eremina et al., 2003).As proliferation of the nascent nephron continues, the proximal and distal tubule segments become convoluted while the region between them grows down into the medullary zone to form the Loop of Henle (Neiss, 1982).Nephrons located in superficial or midcortical regions of the kidney possess short loops of Henle that turn within the cortex or outer medulla zone.More deeply located nephrons (juxtamedullary nephrons) have long loops of Henle that descend into the inner medulla region (Hebert et al., 2001).In addition to the loop of Henle, metanephric nephrons are also distinguished from other nephron types by the macula densa, a population of salt-and fluid-sensing cells in the lining of the distal tubule (see Figure 1).These cells make contact with the parent glomerulus of the nephron and form part of a tubuloglomerular feedback system that couples distal nephron flow with glomerular filtration rate and ensures that the flow through the nephron is tightly controlled (Castrop, 2007).

Molecular mechanisms of metanephric nephron formation
Gene targeting experiments identified Wnt9b and Wnt4 as being necessary for pre-tubular aggregate formation and renal vesicle formation, respectively (Carroll et al., 2005;Kispert et al., 1998;Stark et al., 1994).Wnt9b is expressed throughout the UB-derived collecting duct system (excluding the UB tips) and is considered the primary UB-derived paracrine signal that induces the formation of pre-tubular aggregate cells from the cap mesenchyme (Carroll et al., 2005).Despite the widespread expression pattern of Wnt9b throughout the collecting system only a small subset of cap mesenchyme cells activate a nephrogenic program, thus indicating that additional regulatory molecules must limit the action of Wnt9b.One such factor is Six2, which is expressed by the cap mesenchyme and functions to suppress the ectopic formation of pre-tubular aggregates on the distal side of the UB tip (Kobayashi et al., 2008;Self et al., 2006).Ectopic nephron induction does not occur in compound mutants defective in both Six2 and Wnt9b, consistent with Six2 acting as a suppressor of the nephron-inducing activity of Wnt9b (Kobayashi et al., 2008).However, the nature of the Six2-mediated repression of nephrogenesis and whether it acts directly on Wnt signaling is not known.
Wnt4 is expressed by the pre-tubular aggregates and is postulated to work in an autocrine manner to propagate the initial Wnt signal and complete the transition to the renal vesicle stage.Both Wnt9b and Wnt4 signal via the canonical β-catenin pathway but may use different receptors and act in a linear pathway as Wnt9b is unable to induce nephrogenesis in Wnt4 mutant mesenchyme in vitro (Park et al., 2007).Gain-of-functon studies examining the effect of sustained β-catenin signaling in the metanephric mesenchyme suggest that although Wnt signaling is essential during the early phases of the nephrogenic program, it must be attenuated at later stages in order for nephron progenitors to undergo a mesenchymal-to-epithelial transition (Kuure et al., 2007;Park et al., 2007;Schmidt-Ott et al., 2007).

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A number of studies have begun unraveling the epistatic interactions between Wnt signaling and functionally important nephrogenic genes.Although the circuitry is likely to be more complex, current data suggest that Wnt9b initially activates the expression of Wnt4, Fgf8, and Pax8 in the pre-tubular aggregate, and then Wnt4 maintains the expression of these genes and induces Lhx1 (perhaps in conjunction with FGF8; Grieshammer et al., 2005;Kobayashi et al., 2005;Stark et al., 1994).Lhx1 transcripts are significantly downregulated in Pax2/Pax8 compound heterozygotes (consistent with similar observations found in the nephric duct; see section 4), whereas expression of Wnt4 and Fgf8 are unaffected (Narlis et al., 2007).These data suggest that Pax2 and Pax8 may act downstream of Wnt4 to induce/maintain Lhx1 expression in the pre-tubular aggregate and renal vesicle.In addition, Pax2 and Pax8 are required for nephron survival (Narlis et al., 2007).Conditional inactivation of Lhx1 in the cap mesenchyme has demonstrated a requirement of Lhx1 for the progression of the renal vesicle to the comma-shaped body stage (Kobayashi et al., 2005;Potter et al., 2007).Interestingly, expression of the secreted Wnt antagonist Dkk1 is down-regulated in the renal vesicles of Lhx1 mutants raising the possibility that a Wnt4-Pax2/8-Lhx-Dkk1 pathway may provide the negative feedback loop needed to attenuate Wnt signaling following the initial activation of the nephrogenic program (Potter et al., 2007).
Little is known about the mechanisms responsible for generating the segmentation pattern of the nephron.Current data suggest that proximo-distal patterning begins very early during nephrogenesis as transcripts for Brn1/Pou3f3, encoding a POU domain transcription factor required for distal tubule formation, are restricted to a subset of renal vesicle cells closest to the UB epithelium (Nakai et al., 2003).This localized expression domain is absent in conditional Lhx1 mutants, leading to the suggestion that Lhx1 may act upstream of Brn1/Pou3f3 to establish an early proximo-distal pattern in the renal vesicle (Kobayashi et al., 2005).Interestingly, Pax2/Pax8 compound heterozygotes also display a loss or reduction of the distal tubule segment, consistent with Pax2/8 acting upstream of Lhx1 (Narlis et al., 2007).Both Pax2/8 and Lhx1 are initially expressed throughout the renal vesicle therefore it is not clear how expression of Brn1/Pou3f3 is restricted to presumptive distal progenitors.From early observations, it was hypothesized that the proximo-distal patterning of the nascent nephron occurred in response to signals emanating from the UB (Saxén, 1987).Whether either a Wnt4 or Wnt9b gradient provides such a signal remains to be determined.
There is good evidence to indicate that the Notch signaling pathway is involved in proximo-distal patterning where it appears to act between the renal vesicle and S-shaped body stages to promote the formation of podocytes, proximal tubules, and the loop of Henle (Cheng et al., 2007;Cheng et al., 2003;Wang et al., 2003).At present the downstream transcriptional targets of Notch in the metanephric nephron are not known.Work in Xenopus suggests that one of the members of the Hey family of transcription factors, which are known targets of Notch, may mediate the effects of Notch signaling in the pronephros (Taelman et al., 2006).However, a role for Hey orthologues in metanephric nephron patterning has yet to be demonstrated.In addition to Notch, the RA pathway has been implicated in proximo-distal nephron patterning of the zebrafish pronephric nephron (Wingert et al., 2007).Whether RA is involved in metanephric nephron patterning, in addition to its effects on UB branching, is unknown.

Concluding remarks
Kidney development in amniotes is unique with respect to the other organs in that three separate kidney types arise during embryogenesis.From an evolutionary perspective, the acquisition of additional kidney structures is thought to have occurred during the transition of a freshwater protovertebrate to a dry terrestrial environment (Smith, 1959).The pronephric kidney in lower vertebrates with freshwater larvae, such as Xenopus and zebrafish, plays a critical role in water excretion and prevents the embryo from dying an early death by edema.As the animal grows, additional renal function is necessary in order to cope with the added demands on waste excretion and fluid homeostasis.Therefore, the mesonephric kidney may have evolved in response to greater body mass and associated factors such as increased blood pressure (Vize et al., 1997).The metanephric kidney, with its unique water conserving ability, was the adaptation that allowed amniotes to live and breed on dry land.
In mammals, the embryo is protected from osmotic challenges coming from the external environment by virtue of in utero development, while the problem of waste excretion is ameliorated by the allantois and placenta.Thus, the mammalian embryo has a reduced requirement for the pronephric and mesonephric kidneys and in the case of the mouse these have regressed to rudimentary structures that are short-lived.The (pro)nephric duct has been retained, as the metanephric kidney is dependent upon it as the source of the ureteric epithelium, while some of the mesonephric tubules are co-opted in males for the epididymal ducts of the testis.
Each kidney type is comprised of similar cell types and performs common renal functions.It is not surprising then, that the genes involved in the formation of one kidney type are re-employed in the others.This means that the study of gene function in one kidney type, such as the use of Xenopus and Zebrafish to examine genetic hierarchies

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Mouse kidney development involved in pronephros development, is likely to yield information that is useful to all kidney types.Ultimately however, a detailed understanding of metanephric kidney development can only come from the study of these genes in mammals.In the past, analyzing the function of murine genes central to the development of all kidney types was hampered by early nephric duct defects preventing an assessment of gene function in the metanephros.This has now been largely overcome by employing Cre-Lox technology and the generation of nephric duct-and metanephric mesenchyme-restricted Cre recombinase lines.As additional lines are made, it should be possible to inactivate genes in smaller, lineage-restricted populations of cells, thus providing the level of precision and temporal control needed to unravel the complex epistatic relationships currently hindering the field.A number of renal genes have been implicated in human disease, including PAX2 (renal-coloboma syndrome), WT1 (Wilms' tumor and urogenital disorders), SIX1 and EYA1 (branchio-oto-renal syndrome), GATA3 (HDR syndrome), and SALL1 (Townes-Brocks syndrome; (Dressler, 2006).Thus, a greater understanding of their role during metanephric kidney development will provide a molecular basis for the pathogenesis of these diseases and may lead to new therapeutic or preventative treatments.
Knowledge of embryonic kidney development will also form the foundation for developing stem cell-based strategies to treat renal disease.Some of these approaches are based on the directed differentiation of embryonic stem (ES) or other multipotent cells into kidney cells using cocktails of growth factors followed by transplantation into embryonic or adult kidneys (Bruce et al., 2007;Kim and Dressler, 2005;Kobayashi et al., 2005;Schuldiner et al., 2000;Vigneau et al., 2007).At present, this approach has yielded limited success but will likely improve with a better understanding of the genetic hierarchies governing the formation of the different kidney types.For example, in order to make metanephric mesenchyme from pluripotent stem cells it may be necessary to first convert these cells into Pax2/8 + and Odd1 + intermediate mesoderm and then direct them into a metanephric mesenchyme fate by inducing factors such Eya1, Six2, and Hox11.Recent studies in vivo have shown that ectopic expression of Hox11 in cranial portions of the nephrogenic cord, where it is not normally expressed, is sufficient to induce Six2 expression and transform mesonephric nephrons into more metanephric-like nephrons (Mugford et al., 2008).Thus, the activation of single regulatory factors in stem cell-derived intermediate mesoderm may be sufficient to initiate metanephric mesenchyme formation in vitro.It is unreasonable to hope for the generation of a complete kidney in vitro, however specific cell types, such as the cap mesenchyme, may have therapeutic potential.In the mouse, the cap mesenchyme is lost at postnatal day 3 and nephrogenesis ceases abruptly.In contrast, the UB still expresses Wnt9b at this time and retains the ability to induce nephrons and promote embryonic metanephric mesenchyme survival in vitro (Hartman et al., 2007).Although it is not known how long the nephron-inducing activity of the postnatal UB lasts, it raises the possibility that the transplantation of ES-cell derived cap mesenchyme into newborn or adult kidneys could lead to a restoration of nephrogenesis and a potential therapy for renal defects and disease.
The ability to differentiate pluripotent stem cells into renal cells in vitro will also be useful for studying kidney disease in humans.The recent discovery that somatic cells can be converted into ES-like cells, called induced pluripotent stem cells (iPS) now makes it relatively easy to create a multitude of disease-specific iPS lines (Park et al., 2008;Yamanaka, 2008).Being able to create specific renal cell lineages, such as proximal and distal tubular epithelial cells and podocytes, from patients with renal disorders will provide valuable in vitro tools to dissect the pathogenesis of diseases such as glomerulopathies and polycystic kidney disease.
One of the limitations of using pluripotent stem cell-derived tissues for cell-based therapies is the risk of teratoma formation (Little, 2006).Hence, there is an ongoing search for a resident renal stem cell that would comprise a more therapeutically tractable population to target.The mammalian kidney is known to possess a limited ability to repair the tubular epithelium of damaged nephrons (Humphreys and Bonventre, 2007).Whether this repair is mediated by the dedifferentiation and proliferation of surviving epithelial cells or whether a resident renal stem cell is involved has become the subject of recent investigation.Although candidate renal stem cells have been found in the renal papilla, tubular epithelium, and the urinary pole of the glomerulus, in vivo genetic lineage-labeling and serial transplantation experiments are needed in order to confirm their stem cell properties (Gupta et al., 2006;Lazzeri et al., 2007;Maeshima, 2007;Maeshima et al., 2006;Oliver et al., 2004;Sagrinati et al., 2006).A recent fate-mapping analysis of ischemiareperfusion injured kidneys showed that surviving tubular epithelial cells are the predominant source of the regenerated tissue (Humphreys et al., 2008).While this experiment rules out an extra-tubular source of renal stem cells, it does not exclude the possibility that a resident epithelial progenitor/stem cell is responsible for the repair.Alternatively, each epithelial cell in the nephron may possess an inherent ability to dedifferentiate, proliferate, and re-differentiate into an epithelial cell following damage.There is some evidence to suggest that re-differentiating epithelial cells express embryonic renal genes such as Pax2 (Villanueva et al., 2006).This suggests that tubular regeneration may recapitulate aspects of renal development.If so, then the study of embryonic kidney development may provide insights into the mechanism of renal repair following acute kidney injury.

Mouse kidney development
In summary, elucidating the molecular basis of kidney development will increase our understanding of renal birth defects and disease, provide a foundation for directing the differentiation of pluripotent stem cells into clinically useful renal cells, and further our knowledge of epithelial repair following kidney injury.While there is still much to be learnt in each of these arenas, there is clearly much to be gained.

Figure 2 .
Figure 2. Location of the intermediate mesoderm/nephrogenic cord.Schematic representation of a mouse embryo at E9.5 (left) and a cross-section through the trunk (right) showing the position of the intermediate mesoderm/nephrogenic cord.

Figure 3 .
Figure 3. Overview of kidney development.Mouse kidney development begins at E8.5 with the formation of the nephric duct primordium (blue) from the nephrogenic cord (yellow).Rostral nephric duct precursors are lost by apoptosis while caudal cells persist and grow towards the cloaca.As it extends down the trunk the nephric duct induces the formation of mesonephric tubules in the adjacent nephrogenic cord.Only the rostral mesonephric tubules become joined to the nephric duct.At E10.5, an outgrowth called the ureteric bud forms from the nephric duct near the cloaca.The ureteric bud grows into a specialized population of nephrogenic cord cells (red) called the metanephric mesenchyme.Reciprocal inductive interactions between the ureteric bud and the metanephric mesenchyme lead to repeated branching of the ureteric bud and the formation of metanephric nephrons from the metanephric mesenchyme (not shown).

Figure 4 .
Figure 4.A model of potential epistatic interactions occurring between early-acting transcription factors in the nephrogenic cord at the level of the presumptive metanephros.

Figure 5 .
Figure 5. Key molecular pathways involved in early metanephric kidney development.At E10.5, the metanephric mesenchyme (red) comprises a unique subpopulation of the nephrogenic cord (yellow).Expression of the Glial-derived neurotrophic factor (Gdnf) is resticted to the metanephric mesenchyme by the actions of transcriptional activators, secreted factors, and inhibitors.GDNF binds the Ret receptor and promotes the formation of the ureteric bud, an outgrowth from the nephric duct (blue).Ret initially depends upon the Gata3 transcription factor for its expression in the nephric duct.Spry1 acts as an intracellular inhibitor of the Ret signal transduction pathway.BMP4 inhibits GDNF signaling and is in turn inhibited by the Grem1 binding protein.At 11.5, the ureteric bud has branched, forming a T-shaped structure.Each ureteric bud tip is surrounded by a cap of condensed metanephric mesenchyme.Reciprocal signaling between the cap mesenchyme and ureteric bud, as well as signals coming from stromal cells (red), maintain expression of Ret in the bud tips and Gdnf in the cap mesenchyme.Nephrons are derived from cap mesenchyme cells that form pretubular aggregates and then renal vesicles on either side of each ureteric bud tip.Wnt9b and Wnt4 induce nephron formation and are necessary for maintaining ureteric bud branching.The Six2 transcription factor prevents ectopic nephron formation.BMP7 promotes survival of the cap mesenchyme.Not all genes implicated in metanephros formation are shown for clarity (see text for further details).Green arrows indicate the ligand-receptor interaction between GDNF and Ret.Black arrows indicate the epistasis between genes but in most cases it is not known if the interactions are direct.T-shaped symbols indicate inhibitory interactions.

Figure 6 .
Figure 6.Metanephric nephron formation.Nephrons arise from pretubular aggregates, a subpopulation of the cap mesenchyme, in response to Wnt9b.Early molecular markers of pretubular aggregates are Pax8, Fgf8, and Wnt4.Wnt4 maintains the expression of these genes, induces Lhx1, and converts the pretubular aggregate into an epithelial vesicle.The renal vesicle displays polarized expression of the Brn1/Pou3f3 transcription factor gene in presumptive distal nephron precursors.Growth of the renal vesicle leads to the stereotypical formation of comma-and S-shaped bodies.Notch2 signaling is necessary for the specification of proximal nephron fates (podocytes and proximal tubule).Angioblasts invade the proximal cleft of the S-shaped body and contribute to the glomerular capillary.The distal portion of the S-shaped body fuses with the collecting duct.