Sensational Placodes: Neurogenesis in the Otic and Olfactory Systems

This is a copy of the final published version of a paper published via gold open access in Developmental Biology. This open access article is distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. a b s t r a c t For both the intricate morphogenetic layout of the sensory cells in the ear and the elegantly radial arrangement of the sensory neurons in the nose, numerous signaling molecules and genetic determinants are required in concert to generate these specialized neuronal populations that help connect us to our environment. In this review, we outline many of the proteins and pathways that play essential roles in the differentiation of otic and olfactory neurons and their integration into their non-neuronal support structures. In both cases, well-known signaling pathways together with region-specific factors transform thickened ectodermal placodes into complex sense organs containing numerous, diverse neuronal subtypes. Olfactory and otic placodes, in combination with migratory neural crest stem cells, generate highly specialized subtypes of neuronal cells that sense sound, position and movement in space, odors and pheromones throughout our lives. Introduction The vertebrate ear and nose share interesting similarities as well as important differences in their modes of sensation. Both sensory systems can detect a vast array of distinct environmental stimuli: the human nose can detect up to 400,000 different odors (Mori et al., 2006), while the inner ear can distinguish a wide range of sounds by amplitude, quality and frequency, and detect different vestibular stimuli (gravity, and linear and angular acceleration). However, the strategies employed by the nose and the inner ear differ significantly regarding the modes of transmission to the brain and discrimination between distinct inputs. Whereas olfactory sensory neurons (OSNs) are primary sensory receptor cells, with axons that project directly to the olfactory bulb, hair cells of the inner ear are secondary sensory receptor cells, lacking an axon. Hair cells convey sound and balance information to the brain indirectly via afferent auditory and vestibular neurons in the VIIIth ganglion (ganglion of the VIIIth (statoacoustic) cranial nerve) (Fig. 1A and B). For the purposes of this review, we will consider both otic neurons and sensory hair cells as neuronal cell types, and use the terms neurogenesis and sensorigenesis, respectively, to describe their generation. Otic and olfactory neurogenesis are highly similar processes, each …


Introduction
The vertebrate ear and nose share interesting similarities as well as important differences in their modes of sensation. Both sensory systems can detect a vast array of distinct environmental stimuli: the human nose can detect up to 400,000 different odors (Mori et al., 2006), while the inner ear can distinguish a wide range of sounds by amplitude, quality and frequency, and detect different vestibular stimuli (gravity, and linear and angular acceleration). However, the strategies employed by the nose and the inner ear differ significantly regarding the modes of transmission to the brain and discrimination between distinct inputs. Whereas olfactory sensory neurons (OSNs) are primary sensory receptor cells, with axons that project directly to the olfactory bulb, hair cells of the inner ear are secondary sensory receptor cells, lacking an axon. Hair cells convey sound and balance information to the brain indirectly via afferent auditory and vestibular neurons in the VIIIth ganglion (ganglion of the VIIIth (statoacoustic) cranial nerve) ( Fig. 1A and B). For the purposes of this review, we will consider both otic neurons and sensory hair cells as neuronal cell types, and use the terms neurogenesis and sensorigenesis, respectively, to describe their generation. Otic and olfactory neurogenesis are highly similar processes, each following a sequence of commitment to a neural fate, initiation of neurogenic divisions to generate neuronal precursors and differentiation via the expression of bHLH genes. In the olfactory system, sensory neurons are specialized to each detect a single odorant. In the mouse, for example, there are 1200 distinct odorant genes, with generally only one (or a few) expressed by each OSN, thus determining the cell's spectral response (Buck and Axel, 1991). No such receptor specificity exists in the inner ear hair cells. Instead, mechanical forces displace specialized stereociliary bundles such that deflection of the bundles opens ion channels that modulate the cells' membrane potential (Corey, 2009). In the ear, sensory epithelia responsible for detection of auditory and vestibular inputs are segregated into distinct compartments, and along the mammalian cochlea, differences in frequency sensitivity generate a tonotopic map that in turn is transmitted to the brain. Here, we review current knowledge of the process of development of the olfactory and otic systems, describing their common traits and highlighting their interesting differences, particularly with respect to neurogenesis. We also refer the reader to a number of previous excellent reviews (Fritzsch et al., 2006a(Fritzsch et al., , 2006b(Fritzsch et al., , 2010Kelley, 2006bKelley, , 2006aKelley, , 2009Sanchez-Calderon et al., 2007;Alsina et al., 2009;DeMaria and Ngai, 2010;Gokoffski et al., 2010;Treloar et al., 2010;Bazáes et al., 2013;Miyasaka et al., 2013;Rodriguez, 2013).

Origin of olfactory and otic placodes
In vertebrates, all peripheral sensory neurons arise from two specialized regions of ectoderm that form at the border of the neural plate: the cranial placodes and the neural crest. Placodes are regions of condensed ectoderm arising in the head region that give rise to both non-neural (lens and adenohypophyseal placodes) and neural structures. The neurogenic placodes include the olfactory, trigeminal, profundal, lateral line, otic and epibranchial placodes (Schlosser, 2010). Most neurogenic placodes give rise solely to sensory neurons and associated structures. By contrast, the olfactory and otic placodes give rise to both neural and nonneural structures in the nose and the inner ear, respectively. Moreover, throughout development, both organs undergo a series of cellular rearrangements that spatially distribute their emerging cell types in precise anatomical positions.
Development of the placode-derived sensory organs is a multistep process. It starts with subdivision of the embryonic ectoderm into epidermal ectoderm, neural ectoderm and the neural plate border region, as reviewed in Groves and LaBonne (in press) (this volume). While anterior placodal cells (e.g. olfactory, adenohypophyseal, and lens) express Six3, Pax6 and Otx2 and emerge in the late gastrula (Ahrens and Schlosser, 2005;Sjödal et al., 2007), posterior placodal cells (e.g. otic and epibranchial) express Irx3, Pax2 and Gbx2, and emerge later at the neurula stage in the lateral posterior neural border (reviewed in Schlosser (2006)). Thus, induction of olfactory and otic placodes occurs at different time points and locations in the early embryo. After induction, both olfactory and otic placodes invaginate (or cavitate in zebrafish), transforming from a thickened sheet of ectoderm into a pit and then an epithelial vesicle that is initially a single cell layer thick. Subsequently, the olfactory and otic epithelia transform into multilayered structures and undergo neurogenesis. The otic placode must undergo further extensive morphogenesis to give rise to the semicircular canal ducts and sensory chambers of the inner ear.

Early establishment of neural competence and a neurogenic domain
During placodal development, a critical first step is the delineation of neurogenic versus non-neurogenic domains in the emerging placode. Several models for placode induction and acquisition of neurogenic competence have been discussed in the literature. One possibility is that induced placodes are inherently neurogenic. Alternatively, there may be a more general neurogenic inductive event, followed by restriction or independent specification of neurogenic and non-neurogenic fates. Interestingly, regardless of the sequence of events, similar underlying molecular programs are involved in both the otic and olfactory placodes (Fig. 1C).

Olfactory
Olfactory placodal cells are specified at the gastrula stage (Hamburger and Hamilton stage 4 (HH4)). Explants isolated from the anterior border region give rise to cells of either lens or olfactory identity in distinct regions, while slightly later, at the neural fold stage (HH8), olfactory and lens placodal cells become spatially separated (Sjödal et al., 2007). Explants of presumptive olfactory tissue isolated from both gastrula and neurula stage embryos cultured in vitro give rise to neuronal cells of olfactory placodal identity which express markers for olfactory post-mitotic neurons (Sjödal et al., 2007;Maier and Gunhaga, 2009). This suggests that, once specified, presumptive olfactory placodal cells have neurogenic potential.
As development proceeds, presumptive olfactory placodal cells mature, and change in their responsiveness to BMP signaling. Whereas at early stages BMP induces prospective lens placodal character in olfactory placodal explants, at later stages, BMP signaling promotes respiratory epithelial non-neurogenic olfactory fates in chick and mouse (Sjödal et al., 2007;Maier et al., 2010). Fgf8 is expressed anteriorly, and is required for the emergence of sensory olfactory epithelial cells. FGF signals also act to restrict the range of BMP activity in the nasal epithelium, limiting the extent of the respiratory epithelium (Maier et al., 2010). Thus, BMP signaling at later stages is required for the emergence of the non-neurogenic olfactory domain, while FGF signaling is required to maintain the neurogenic region. Raldh3 expression overlaps with the Fgf8 expression domain, whereas Bmp4 is expressed posteriorly. This raises the interesting possibility that RA, FGF and BMP signaling act to subdivide the olfactory placode and regulate the coordinated emergence of neurons (Fig. 1C).
Hes1 homologs are expressed in the future olfactory domain, where they act as prepatterning genes that define the neurogenic region. In addition, they play a later role in neurogenesis in mouse, chick and zebrafish (Cau et al., 2000;Thisse and Thisse, 2005;Maier and Gunhaga, 2009). These data suggest conserved functions of Hes-like genes during olfactory development throughout vertebrates. In addition to Hes genes, mutation of Sox2 and its cofactor Oct1 affects nasal development upstream of Pax6 (Donner et al., 2007), suggesting a role for these factors in olfactory development.

Otic
The otic placode becomes subdivided into an anterior neurogenic and posterior non-neurogenic domain. The neurogenic domain gives rise to the neurons of the VIIIth ganglion (statoacoustic ganglion, vestibuloacoustic ganglion, or vestibular and spiral ganglia, depending on species). This domain is likely to overlap with a broad zone of sensory competence that gives rise to the sensory hair cells in chick and mouse (Satoh and Fekete, 2005;Raft et al., 2007), since macular hair cells derive from a common neurog1-positive precursor that also gives rise to neurons (see below). In the fish, sensory hair cells arise at both the anterior and posterior poles of the otic vesicle (Haddon and Lewis, 1996). Although both sensory hair cell and neuronal lineages share many common regulatory features, recent data in zebrafish indicate that competence to form the neuronal lineage precedes that to form the sensory lineage (Hans et al., 2013). Manipulations in dlx3b/4b or foxi1 reveal a role for these transcription factor genes in acquisition of sensory versus neuronal competence, respectively. This developmental decision occurs early, during induction of the otic-epibranchial precursor domain. In embryos carrying a homozygous deletion that removes dlx3b, dlx4b and sox9a genes (b380 mutants), almost all otic fates, including the sensory lineage, are lost. Nevertheless, expression of otic neuroblast markers (neurod, cdh6) persists. Conversely, mutation of foxi1 compromises otic neurogenesis, while sensory cells still form. Morpholino-mediated knockdown of foxi1 in b380 mutants results in the loss of both sensory and neuroblast fates in the ear (Hans et al., 2013). Thus, in zebrafish, otic neuronal competence is critically dependent on foxi1 function, while dlx3b/4b genes promote sensory competence. It still remains to be elucidated whether a similar mechanism occurs in other species.
Sox3 and Sox2 have been implicated in acquisition of neural (both sensory and neuronal) competence downstream of FGF signaling (Abelló et al., 2010). Disruption of Sox2 in mouse impairs formation of the sensory domain (Kiernan et al., 2005). Sox2 directly binds to the Atoh1 promoter and activates its expression (Kiernan et al., 2005;Neves et al., 2012), acting in a feed-forward loop with other bHLH factors, and in co-operation with Six1, upstream of Atoh1 (Ahmed et al., 2012;Neves et al., 2012). In addition, Sox2, possibly together with Sox3, drives neuronal differentiation in the chick ear (Neves et al., 2012) and may play a role in acquisition of otic sensory competence in the zebrafish (Sweet et al., 2011).
Tbx1, a T box transcription factor, acts to restrict the extent of the neurogenic domain in the otic vesicle: it is expressed in the non-neurogenic domain of the otic epithelium in mouse and zebrafish, and the neurogenic domain is expanded in Tbx1 mutants in both species (Raft et al., 2004;Radosevic et al., 2011). In zebrafish, Tbx1 acts through the Hairy/Enhancer of Split (Hes) gene her9, which is co-expressed with tbx1. Morpholino-mediated knockdown of her9 results in a similar expansion of the neurogenic domain (Radosevic et al., 2011). At least four additional Heslike genes are expressed in the otic placode and vesicle in zebrafish (Thisse and Thisse, 2005;Gajewski et al., 2006), raising the possibility that Hes-like genes also might be involved in neurogenic patterning.
Expression of Tbx1 in the ear is regulated by extrinsic signaling factors. The retinoic acid (RA) synthesizing enzyme gene Raldh2 is expressed in the mesoderm surrounding the otic placode and is required to specify Tbx1-positive cells in zebrafish, chick and mouse (Bok et al., 2011;Radosevic et al., 2011). It is likely that RA regulates Tbx1 expression directly during a narrow temporal window (Bok et al., 2011). By contrast, otic tbx1 expression is repressed in zebrafish embryos with over-active Hedgehog (Hh) signaling (Hammond et al., 2010), and is induced by Hh inhibition (Radosevic et al., 2011). Thus, RA and Hh signaling appear to play a role in positioning the boundary between neurogenic and nonneurogenic domains in the ear.
BMP signaling also affects gene expression (Lmx1b) in the nonneurogenic domain of the otic placode/vesicle/cup, but has no effect on Sox3 expression and neurogenic fate (Abelló et al., 2010). In chick, members of the Delta/Notch pathway are differentially expressed in the otic placode/cup: Delta1, Hes5 and Lunatic fringe are restricted to the neurogenic domain, while Serrate1 and Hairy1 are expressed in the non-neurogenic domain (Abelló et al., 2007). Notch inhibition in neurula stage chick embryos causes expansion of the non-neurogenic domain and overproduction of neural precursors in the remaining neurogenic region (Abelló et al., 2007). Thus, Notch signaling is required to restrict the nonneurogenic domain. In zebrafish mindbomb mutants, in which Notch signaling is disrupted, increased numbers of neuroblasts and sensory hair cells develop in the ear (Haddon et al., 1998;Haddon et al., 1999).
FGF genes are also expressed around the otic placode/vesicle and later in the otic vesicle itself. Like BMPs, FGFs play important roles at multiple steps of otic development. In both chick and zebrafish, otic Sox3 expression is dependent on FGF signaling (Nikaido et al., 2007;Sun et al., 2007;Abelló et al., 2010). In zebrafish embryos treated with the FGF inhibitor SU5402 after formation of the otic placode, expression of neurod in the developing otic ganglion is reduced, whereas ubiquitous overexpression of fgf3 at the 10 somite (early placode) stage results in the duplication of a neurod-expressing domain at the posterior of the ear (Hammond and Whitfield, 2011). Taken together, these results demonstrate both the requirement and sufficiency of FGF for early otic neurogenic development, in addition to its roles in the neuronal (Alsina et al., 2004;Vemaraju et al., 2012) and sensory lineages (Millimaki et al., 2007;Sweet et al., 2011) at later stages.
In conclusion, the same signaling pathways regulate the early patterning events that lead to the generation of neurogenic and non-neurogenic territories, with some similarities and some differences between the olfactory and otic placodes (Fig. 1C). In both systems, FGF signaling promotes neurogenic character, whereas BMP promotes non-neurogenic character. RA, on the other hand, acts as a positive regulator of neurogenic fate in the olfactory placode, but acts as a negative regulator of neurogenic fate in the otic placode.

Dual placode and neural crest contributions to otic and olfactory derivatives
The notion that placodes contribute exclusively to all cell types in mature sensory organs-with the known exceptions of peripheral glia of all sensory ganglia, and intermediate cells of the mammalian cochlea, which originate in the neural crest-has been challenged over the last few years. Recently, a neural crest contribution has been reported for both neuronal and nonneuronal components of the otic and olfactory systems (Dutton et al., 2009;Barraud et al., 2010;Forni et al., 2011;Freyer et al., 2011;Katoh et al., 2011;Saxena et al., 2013).
Occasional contribution of neural crest cells to the ear has been demonstrated in zebrafish embryos. Single-cell labeling of neural crest cells located at the level of rhombomere 4 revealed a small proportion of clones that contributed to the early otic vesicle, though most of these cells were lost by the third day of development (Dutton et al., 2009). Transgenic labeling studies in mouse, using driver lines expressing GFP in neuroepithelial cells, claim a more substantial neuroepithelial (and possibly neural crest) contribution to the inner ear and VIIIth ganglion (Freyer et al., 2011). However, these results remain controversial, given the recently raised problems with some of the Cre driver lines used for these studies (Lewis et al., 2013).
In zebrafish, a recent study provides support for the neural crest origin of microvillous sensory neurons within the olfactory epithelium using lineage analysis of early migrating neural crest cells via photoconversion (Saxena et al., 2013). Neural crest cells surround the olfactory capsule and a subpopulation intercalates into the olfactory epithelium, differentiating into microvillous neurons. Moreover, ablation of the neural crest caused a depletion of microvillous neurons in the nose but had only a minimal effect on the ciliated neurons, suggesting that placodal cells cannot compensate for the loss of neural crest-derived sensory neurons. Taken together, these studies indicate that neural crest cells may contribute to various lineages in the nose and inner ear of zebrafish. It is not clear whether this finding can be generalized to mammals; more detailed lineage studies are necessary to resolve this important question.
One additional cell type that is now considered to be a neural crest derivative in several species is the olfactory ensheathing cell. Olfactory ensheathing cells myelinate the olfactory nerve and are of great interest due to their clinical potential to promote axon regeneration in the CNS (Kawaja et al., 2009). Although it had been assumed that olfactory ensheathing cells derive from the olfactory placode (Couly and Le Douarin, 1985), fate mapping studies in chick and mouse recently have suggested that olfactory ensheathing cells are in fact neural crest-derived (Barraud et al., 2010;Forni et al., 2011;Katoh et al., 2011). In addition, cells of neural crest origin have been detected in the embryonic and postnatal olfactory epithelium, where they may contribute to horizontal basal cells, globose basal cells, sustentacular cells and Bowman glands/ducts (Katoh et al., 2011). Forni and colleagues (Forni et al., 2011) detected a similar range of neural crest-derived cell types as well as olfactory marker protein (OMP)-positive olfactory sensory neurons and a neural crest contribution to the vomeronasal organ. As mentioned above, the issues with many of the Cre lines used in the experiments mean that further confirmation will be required for these results.
In the chick ear, cochleo-vestibular glia derive from neural crest cells (D'Amico-Martel and Noden, 1983;Hemond and Morest, 1991) and develop in tandem with the otic sensory neurons to guide their projection to the CNS (Sandell et al., 2014).

Neurogenesis in the olfactory and otic placodes
In the olfactory system, neurogenesis occurs throughout life such that there is a steady-state production of OSNs to replace damaged neurons. Two phases of olfactory neurogenesis have been described . First, primary neurogenesis occurs in the invaginating placode, establishing the basic structures of the olfactory epithelium and giving rise to a number of migratory neuronal cell populations that move to the olfactory bulb (Valverde et al., 1993;Drapkin and Silverman, 1999;Fornaro et al., 2003;Kawauchi et al., 2004;Maier and Gunhaga, 2009;Miller et al., 2010). Primary neurogenesis starts at approximately E10 in mouse and HH14 in chick Maier and Gunhaga, 2009) (Fig. 2G). A second wave of neurogenesis, termed established neurogenesis, occurs in the maturing pseudo-stratified epithelium (Fig. 2H). Here, stem cells give rise to transit amplifying neuronal progenitors, which in turn form immature neuronal precursors and finally give rise to OSNs (Calof et al., 2002).
Otic neurogenesis begins at the otic placode stage and proceeds until late stages of otic development ( Fig. 2A-F and N). The duration of otic neurogenesis has not fully been determined, but in chick, neurogenesis proceeds at least until E6 (Bell et al., 2008). From E9 in mouse and 17 hours post fertilization (hpf) in zebrafish, neuroblasts begin to delaminate from the otic vesicle, migrate away and coalesce anteriorly to the otic vesicle to form the VIIIth ganglion (Carney and Silver, 1983;Haddon and Lewis, 1996;Vemaraju et al., 2012). In zebrafish, otic neuroblast specification and delamination peaks at around 24 hpf but continues until 42 hpf (Haddon and Lewis, 1996;Vemaraju et al., 2012). Proliferation continues in neuroblasts from the statoacoustic ganglia in a series of transit-amplifying divisions that expand the pool of neuronal progenitors . In contrast to olfactory neurogenesis, no otic neurogenesis during adulthood has been reported in mammals to date.

Intrinsic factors regulating neurogenesis
As cells progress from neural progenitor to mature neuron, distinct sets of transcription factors are expressed at different developmental times. Members of the Sox-B1-type SRY transcription factor family (Sox2) and of the bHLH transcription factor family (Neurog1) are expressed in most neurogenic tissues, including the otic and olfactory placodes ( Fig. 2N and O).

Intrinsic factors regulating olfactory neurogenesis
During murine olfactory development, Sox2 is expressed throughout the prospective neuroepithelium of the invaginating placode from E10.5 onwards, in a pattern similar to Hes1/Hes5 Schematic drawing comparing the prospective neurogenic region in the otic placode from a 14 somite stage (ss) zebrafish embryo and a 14ss chick embryo. In the zebrafish, the sensory marker atoh1b is already expressed at 14ss (Millimaki et al., 2007), slightly ahead of the neurogenic marker neurog1 at 16ss (Radosevic et al., 2011). By contrast, in the chick, expression of ngn1 appears before the expression of sensory markers.  (Cau et al., 2000;Kawauchi et al., 2005). Sox2 is co-expressed with Fgf8 at the rim of the invaginating placode. In Fgf8 null mutant mice, these Sox2-expressing cells undergo apoptosis, and neurogenesis fails to occur . Later (from E11.5 onwards), Sox2 expression in the olfactory epithelium appears graded (high medial, low lateral). Some Sox2-positive cells coexpress Ascl1 and mainly reside in the medial olfactory epithelium, where they divide rapidly (Tucker et al., 2010). Elevation of Sox2 expression in lateral olfactory epithelium, where it is normally low, enhances neurogenesis. Thus, Sox2 functions as a dosedependent regulator of precursor state in the olfactory epithelium. In the adult olfactory epithelium, Pax6 and Sox2 are expressed in basal cells and are upregulated before Ascl1 expression after damage (Shetty et al., 2005;Guo et al., 2010) (Fig. 2O).
During olfactory epithelial development, Hes genes have been implicated as pre-patterning genes that define the neurogenic domain within the olfactory placode at early stages (Cau et al., 2000;Maier and Gunhaga, 2009). Later, they control the number of neural progenitors by negatively regulating neurogenesis (Cau et al., 2000). Ascl1 is expressed in both the developing and established olfactory epithelium and is a marker for transient amplifying neuronal progenitors (DeHamer et al., 1994;Gordon et al., 1995;Cau et al., 2000;Calof et al., 2002;Beites et al., 2005). Loss of Ascl1 function leads to a severe reduction of OSNs in the olfactory epithelium (Guillemot et al., 1993). Ascl1 acts upstream of Neurogenin1 (Neurog1) and NeuroD in the OSN lineage and is required to initiate OSN differentiation (Cau et al., 1997). In the absence of Ascl1 function, progenitor cells fail to differentiate and levels of both proliferation and apoptosis in the olfactory epithelium increase, with surplus proliferating cells expressing markers of both neuronal progenitors (Ascl1 3 0 UTR) and supporting cells (Steel) . Ascl1-positive cells mature into Neurog1-expressing neurons. Accordingly, olfactory neuron differentiation is blocked in Neurog1 null mutant mice (Cau et al., 2002). The Forkhead family member Foxg1 is expressed in the developing mouse olfactory placode in a pattern similar to Sox2 (Duggan et al., 2008). Foxg1-positive cells are located basally in the olfactory epithelium, and both mice and zebrafish lacking Foxg1 have impaired differentiation of OSNs (Duggan et al., 2008;Kawauchi et al., 2009).
NeuroD is expressed late in Neurog1-positive progenitors when they start differentiating (Cau et al., 1997). After birth, NeuroDpositive cells in mice co-express Runx1 (Theriault et al., 2005), which may act at the transition between immature neuronal precursor and OSN. Runx1 is sufficient to expand the mitotic population in vitro (Theriault et al., 2005), making it a possible co-ordinator of proliferation and differentiation during olfactory neuron development. The LIM-homeobox gene Lhx2 is expressed in both progenitor cells and olfactory neurons (Hirota and Mombaerts, 2004;Kolterud et al., 2004). In Lhx2 null mutant mice, both Ascl1-positive and Neurog1-positive neuronal progenitors are normally distributed, but the expression of Neurod1 and apoptosis markers is increased and expression of late differentiation markers is reduced (Hirota and Mombaerts, 2004;Kolterud et al., 2004).

Intrinsic factors regulating otic neurogenesis
The inner ear expresses members of the atonal family. Neurog1 is the earliest determination factor for the domain of neuronal precursors (Adam et al., 1998;Ma et al., 1998;Andermann et al., 2002). From this region, neuronal precursors are singled out by Notch-mediated lateral inhibition (Adam et al., 1998;Haddon et al., 1998). Cells expressing high levels of Neurog1/Delta1 become neuronal precursors, retaining expression of Sox2/3 and activating Hes5 expression in their neighbors. High levels of Neurog1 or Delta1 activate other bHLH genes such as NeuroD4/ NeuroM followed by NeuroD1 (Adam et al., 1998;Kim et al., 2001;Bell et al., 2008). NeuroD1 has been shown to be essential for neuroblast delamination and survival (Kim et al., 2001) (Fig. 2N).
In the mouse, neuroblasts emigrate from a small domain of the otic vesicle that includes precursors of the utricular and saccular macula (Raft et al., 2007). Interestingly, neuroblasts exiting the epibranchial placodal epithelium in chick do not express characteristic epithelial-to-mesenchymal transition (EMT) markers such as Snail2, nor do they adopt a mesenchymal phenotype (Graham et al., 2007). It remains to be seen if this is a general feature of all placodal neurogenesis; however, the snail2 gene is expressed in the neurogenic region of the zebrafish otic vesicle (Whitfield et al., 2002). Once they have migrated to the site of the VIIIth ganglion, otic neuroblasts express transcription factors such as Islet1 or POU4f1 Radde-Gallwitz et al., 2004), together with the survival factor IGF1 (Camarero et al., 2001). In mouse, neuronal subtype identity (cochlear versus vestibular) correlates with the expression of the zinc finger transcription factor Gata3, which is initially expressed throughout the otic epithelium but becomes largely restricted to auditory neurons (Karis et al., 2001;Lawoko-Kerali et al., 2004;Jones and Warchol, 2009;Lu et al., 2011). Neurons are still generated in Gata3 mutant mice, but a severe reduction in sensory cochlear neurons has been reported (Karis et al., 2001;Duncan and Fritzsch, 2013). The transcription factors Lmx1a and Tlx3 have been implicated in the regulation of vestibular neuron development. Lmx1a is co-expressed with Gata3 in neurogenic regions of the otic vesicle. Mice with disrupted Lmx1a (dreher mutants) have increased numbers of vestibular neurons; Tlx3 is upregulated, but Gata3 is not affected (Koo et al., 2009). Tlx3 is only expressed in vestibular neurons (Koo et al., 2009;Lu et al., 2011), but its precise function is currently unknown. Other factors, such as birth date, position and further signaling may determine whether the neurons innervate auditory or vestibular cells (Bell et al., 2008;Sapède and Pujades, 2010).

Intrinsic factors regulating otic sensorigenesis
Sensory hair cells are produced from sensory stem cells that express Sox2. The shared expression of Sox2 in the neurogenic and sensory stem cells may indicate a putative common progenitor for both hair cells and neurons. However, in chick, data indicate that otic neurons share common progenitors only with hair cells of the utricular macula (Satoh and Fekete, 2005). In mice, cell lineage tracing experiments using the Neurog1 reporter transgenic mouse further support the interpretation that not all hair cells derive from a common progenitor with the neurons. Only hair cells of the utricular and saccular maculae derive from a progenitor expressing Neurog1 at early time points (Raft et al., 2007). Similarly, in zebrafish, a common progenitor giving rise to both sensory neurons and hair cells of the posterior macula has only been described in the posterior domain of the placode (Sapède et al., 2012). Choice of neuronal or sensory fate by the daughter cells of such a common progenitor might depend on the balance between the proneural factors Neurog1 and Atoh1, which cross-regulate each other (Raft et al., 2007). Although the signals that promote the extinction of Neurog1 expression together with an increase of Atoh1 are still not well defined, Notch and BMP4 signaling pathways are likely to be key mediators of this process (Cole et al., 2000;Daudet and Lewis, 2005;Pujades et al., 2006;Kamaid et al., 2010;Jeon et al., 2011) (Fig. 2N).
Activation of the proneural gene Atoh1 is indicative of sensory hair cell differentiation. Loss of Atoh1 in mice or zebrafish results in loss of hair cells; conversely, its over-expression results in ectopic hair cell formation (Bermingham et al., 1999 Liu et al., 2012;Xu et al., 2012;Yang et al., 2012). In chick, sensorigenesis (marked by the expression of Atoh1) lags behind neurogenesis (marked by the expression of Neurog1) by several days (Adam et al., 1998;Pujades et al., 2006). However, in zebrafish, atoh1 expression precedes neurog1 expression (Millimaki et al., 2007;Radosevic et al., 2011). Conditional deletion of Atoh1 function at later stages of cochlear development revealed additional roles in hair cell survival and stereocilia bundle formation (Cai et al., 2013;Chonko et al., 2013). Interestingly, loss of Atoh1 leads not only to a loss of hair cells but also supporting cells (Bermingham et al., 1999;Chen et al., 2002;Driver et al., 2013).
In contrast to its role during neurogenesis, Notch signaling has a dual function in sensorigenesis; it initially promotes a broad sensory fate by a lateral induction mechanism mediated by Jagged1 (Kiernan et al., 2001;Kiernan et al., 2006) and secondly selects hair cells from support cells in a classical lateral inhibition mechanism mediated by Delta1 (Haddon et al., 1998;Lanford et al., 1999;Daudet and Lewis, 2005;Daudet et al., 2007); reviewed in Neves et al. (2013).

Extrinsic factors regulating neurogenesis
Extrinsic signaling molecules control the transition between the stem cell precursor and differentiated fate choice outlined above, together with the acquisition of new expression domains of intrinsic transcriptional regulators. In addition, extrinsic signaling events impact on proliferation, cell survival, cell death and-at later stages of olfactory neurogenesis-cell position in the epithelium.

Extrinsic factors regulating olfactory neurogenesis
During early olfactory development, FGF, BMP, RA and Notch signaling have all been implicated in the regulation of neurogenesis in the invaginating olfactory pit in mouse and chick Maier et al., 2010Maier et al., , 2011Paschaki et al., 2013). These pathways are also implicated in the regulation of olfactory neurogenesis at later stages, both during the embryonic phase of established neurogenesis and postnatally.
At early stages, Fgf8 is expressed in the rim of the invaginating olfactory placode, where it defines a morphogenetic center that is crucial for neurogenesis, cell proliferation and morphogenesis Maier, 2009;Maier et al., 2010). In the absence of FGF signaling, the olfactory pit fails to invaginate in both mouse and chick Maier et al., 2010), and the remaining cells are of respiratory olfactory character (Maier et al., 2010). In part, FGF acts to counteract posteriorly emanating BMP signaling, as pSmad1/5/8 levels are raised in the absence of FGF signaling both in vitro and in vivo (Maier et al., 2010). In mouse, Fgf18 starts to be expressed in the olfactory epithelium from around E12.5  while Fgf2 is expressed in the olfactory epithelium after birth (Hsu et al., 2001;Kawauchi et al., 2004). Addition of FGF2 to sensory epithelial cell cultures derived from late embryonic or mature olfactory epithelium stimulates transient amplifying cell division and the maintenance of stem cells (DeHamer et al., 1994).
In chick, Bmp4 expression starts approximately in the middle of the olfactory pit and reaches all the way posteriorly (Maier, 2009). At these early stages, BMP signaling is critical for the development of the respiratory epithelium, but cells in the sensory part of the olfactory pit express scattered pSmad1/5/8, indicating that BMP signaling is active in prospective sensory cells (Maier, 2009). Loss of BMP signaling in vitro in a chick explant assay blocks primary neurogenesis and cells are Hes5-positive (Maier et al., 2010); Notch signaling, in turn, is required to maintain Hes5-positive progenitor cells in the olfactory epithelium (Maier et al., 2011). The BMP inhibitor Noggin strongly inhibits the formation of neuronal colonies in sensory epithelium dissected from E14.5 to E16.5 (Shou et al., 2000), while BMP ligands show both inhibitory and stimulatory effects on later neurogenesis (Shou et al., 1999(Shou et al., , 2000. Another TGFβ family member expressed in the olfactory epithelium is GDF11 (Nakashima et al., 1999), which plays a role in the established phase of olfactory neurogenesis. Exogenous GDF11, as well as lack of the GDF11 inhibitor Follistatin, decrease proliferation of progenitor cells, thus negatively impacting on neurogenesis (Wu et al., 2003). Conversely, GDF11 null mutant mice have increased numbers of proliferating Neurog1-positive precursors, which ultimately give rise to OSNs. Nevertheless, loss of GDF11 is not sufficient to rescue the phenotype in Follistatin null mutant mice fully, suggesting that additional mechanisms are in place to account for the decrease in neuron numbers (Gokoffski et al., 2011). Both Sox2-positive and Ascl1-positive cells are increased in the olfactory epithelium of ActivinβB null mice (Wu et al., 2003;Gokoffski et al., 2011), affecting the cell fate decision between glial and neuronal lineages (Gokoffski et al., 2011). Taken together, these results suggest that TGFβ signaling is crucial for feedback regulation of progenitor cell populations and fate choices in the olfactory epithelium.
RA emanating from the Raldh3-expressing anterolateral rim of the olfactory pit has been implicated in olfactory epithelium patterning and/or differentiation (LaMantia et al., 2000;Bhasin et al., 2003;Paschaki et al., 2013). In the absence of RA signaling, Pax6-positive cells are reduced in the olfactory epithelium while elevated levels of RA suppress neurite outgrowth in vitro (Paschaki et al., 2013). RA production in the olfactory epithelium persists during late embryonic development into adulthood. In adult mice, all three retinoic acid-producing enzymes (Raldh1, 2 and 3) are expressed in the olfactory epithelium (Niederreither et al., 2002;Peluso et al., 2012). Raldh3 expression is detected in a small population of basal cells in the ventral and lateral epithelium; gain-and loss-of-function data support the idea that RA signaling is involved in maintenance of the epithelium and OSN regeneration after injury (Peluso et al., 2012).

Extrinsic factors regulating otic neurogenesis
Several studies suggest a role for FGF signaling in otic neurogenesis in different species (Mansour et al., 1993;Hossain et al., 1996;Adamska et al., 2000;Pirvola et al., 2000;Adamska et al., 2001;Léger and Brand, 2002;Alsina et al., 2004;Millimaki et al., 2007) but analysis has been complicated due to overall defects in inner ear development. In zebrafish, fgf3 and fgf8 are expressed in and around the anterior otic vesicle and moderate levels of FGF signaling are required for neuroblast specification (Vemaraju et al., 2012). Mature neurons in the VIIIth ganglion start to express fgf5, with ongoing FGF signaling in the VIIIth ganglion serving two functions: firstly to delay differentiation of precursor cells, thus controlling precursor cell maintenance and the production of mature neurons, and secondly to terminate neuroblast specification when a sufficient number of fgf5-positive cells has accumulated (Vemaraju et al., 2012). In mammals, ongoing expression of Fgf10 (Pirvola et al., 2000) might have similar functions in regulating the balance between transit amplifying neuroblasts and differentiating neurons. Thus differential FGF signaling regulates distinct phases of otic neurogenesis.
Sensory cells secrete nerve chemoattractant molecules that influence axon routing. Some of the candidates for exerting a chemoattractant function in the inner ear are the neurotrophins, BDNF and NT3. Both are expressed in sensory patches, while VIIIth ganglion neurons express TrkB and TrkC receptors for BDNF and NT3, respectively (Fariñas et al., 2001). Ectopic expression of BDNF causes rerouting of axons (Tessarollo et al., 2004). In addition, VIIIth ganglion neurons express neuropilin/plexin receptor complexes while the otocyst expresses the repellent semaphorin3A. This prevents the sensory afferent axons from innervating inappropriate locations (Gu et al., 2003;Katayama et al., 2013). Recently, the EphB2 and EphA4 receptors have been shown to regulate the segregation of axonal entries at the brainstem in a cell-autonomous manner (Allen-Sharpley et al., 2013).

Extrinsic factors regulating otic sensorigenesis
Several signaling pathways have been implicated in hair cell formation in the inner ear. Shh is expressed in the developing spiral ganglion and has been shown to inhibit hair cell formation in cochlear explants (Driver et al., 2008;Liu et al., 2010). Shh signaling from the spiral ganglion regulates the time point at which hair cell precursors exit the cell cycle and differentiate (Bok et al., 2013;Tateya et al., 2013). In zebrafish, Shh signaling is required for the formation of hair cells from the saccular macula (Sapède and Pujades, 2010). Together with studies that show a requirement for Shh signaling in the development of auditory structures from the ventral otocyst, this has led to the speculation that Shh signaling was recruited during inner ear evolution to direct the formation of a second sensory patch with distinct auditory function (Riccomagno et al., 2002;Bok et al., 2005;Sapède and Pujades, 2010).
Wnt signaling is implicated at many stages of otic development. The Wnt pathway components are expressed in the chick basilar papilla (Sienknecht and Fekete, 2008) and ectopic activation of the canonical Wnt pathway leads to the formation of ectopic hair cells in chick non-sensory regions (Stevens et al., 2003). Using in vitro and in vivo approaches, a role for Wnt signaling in regulating sensory precursor cell proliferation and hair cell differentiation in the basilar papilla has been suggested (Jacques et al., in press). A similar role has been observed for hair cells in the zebrafish lateral line (Jacques et al., in press).
Both Notch and BMP4 signaling pathways have been implicated in sensory hair cell development (Cole et al., 2000;Daudet and Lewis, 2005;Pujades et al., 2006;Kamaid et al., 2010;Jeon et al., 2011). Expression of Bmp4 marks all the emerging pro-sensory regions in mouse and most in zebrafish (Wu and Oh, 1996;Morsli et al., 1998;Cole et al., 2000;Mowbray et al., 2001). In vitro treatment of the chick otocyst with BMP4 leads to a decrease in the number of Atoh1-positive cells, while treatment with the BMP antagonist Noggin leads to an increase (Pujades et al., 2006). Increased BMP activity upregulates the expression of Id1-3, and the forced expression of Id1-3 is sufficient to reduce Atoh1 expression and to prevent hair cell differentiation (Kamaid et al., 2010).

Neuronal cell types and differentiation in the olfactory and otic systems
The final outcome of neurogenesis in the ear and the nose is a wide variety of neurons and mechanosensory cells, exquisitely tailored for the detection of different sensory inputs. These differ significantly between the olfactory and otic placodes and are described below, and summarized in Fig. 3.

Olfactory sensory neurons
The olfactory epithelium acquires a layered morphology and is populated by three broad classes of OSNs: ciliated, microvillous, and crypt neurons, with the first two being the dominant subtypes and the third present only in some species, including teleosts ( Fig. 3D-H). OSNs can differ within subtypes, and, to a significant extent, across species. In general, the basally located ciliated sensory neurons, the most well-characterized of the OSNs, are responsible for volatile odorant detection, whereas the more apically located (and/or separately located in the vomeronasal organ) microvillous sensory neurons detect pheromones, nucleotides, amino acids and other molecules, depending on the species (Buck, 2000;Sato and Suzuki, 2001;Hansen and Zielinski, 2005). The crypt cells are located at the apical surface and have both microvilli and cilia (Hansen and Zeiske, 1998). Recent work in zebrafish has described the unusual relative homogeneity of these cells, wherein they all express an identical olfactory receptor and target a single glomerulus (Gayoso et al., 2012;Oka et al., 2012;Ahuja et al., 2013).
In addition to OSNs, populations of migratory neuronal cells leave the olfactory placode/pit and move towards the forebrain. Collectively, the heterogeneous populations of migratory cells and the extending OSN axons are termed the "migratory mass". A first wave of migratory neuronal cells (GnRH-negative) is seen directly after onset of neuronal differentiation in the olfactory placode, before OSN axons have emerged from the olfactory placode: these early migratory cells are thought to play a role in establishing a scaffold for the extension of OSN axons slightly later (Croucher and Tickle, 1989;De Carlos et al., 1995;Maier and Gunhaga, 2009) (Fig. 2J). Later migratory cell populations along the forming olfactory nerve include the GnRH-positive neuronal cells that migrate along the olfactory nerve to the hypothalamus and the nervus terminalis (Schwanzel-Fukuda and Pfaff, 1989;Wray et al., 1989aWray et al., , 1989b; (reviewed in Cariboni et al. (2007)), the olfactory ensheathing glia, OMP-positive cells and acetylcholine esterasepositive cells (De Carlos et al., 1995;Miller et al., 2010). Neuroactivity in the olfactory system is modulated both in the olfactory bulb and the olfactory epithelium. The best-described modulatory pathway is via the terminal nerve and GnRH, but other neuropeptides are also present (reviewed in Whitlock (2004), Kawai et al. (2009)).
In mice, the picture is further complicated by the presence of a variety of different microvillous cells in the main olfactory epithelium that may or may not be neuronal in nature. It has been suggested that secondary sensory and/or non-neuronal microvillous cells, possibly in co-operation with ciliated neurons, are involved in chemosensation. Various subtypes and possible roles have been identified to date in multiple publications, often with conflicting conclusions (Rowley et al., 1989;Asan and Drenckhahn, 2005;Elsaesser et al., 2005;Elsaesser and Paysan, 2007;Hansen and Finger, 2008;Lin et al., 2008;Hegg et al., 2010;Ogura et al., 2011). As such, more work is required to determine comprehensively how many subtypes of microvillous cells exist in the mammalian olfactory epithelium, whether any of these have direct neuronal sensory roles, and what proportion have secondary sensory properties as opposed to solely supporting roles. These microvillous cells are reminiscent of the integrated ciliated/microvillous architecture seen in teleosts, and add further to the debate regarding the presence and mechanisms of pheromone-sensing/ vomeronasal OSNs in humans.

Otic sensory hair cells
Hair cells are the sensory unit of the inner ear. The hair cell bundle is composed of actin-rich stereocilia (a type of microvilli) that are linked to each other by a series of connecting links (tip links, top connectors and ankle links). Protein constituents of the tip link include Protocadherin15, Cadherin23 and Harmonin, which together act to transduce the mechanical force to the anion mechanotransducer channel (reviewed in Schwander et al. (2010), Richardson et al. (2011), Kazmierczak and Müller (2012)). The hair bundle is polarized in the plane of the epithelium, with the kinocilium positioned on one side of the hair bundle, nearest the tallest stereocilia, and connected to it by kinociliary links. This arrangement gives the hair cell its directional sensitivity, with maximum stimulation occurring when the stereociliary bundle is deflected in the direction of the kinocilium. Examples of polarity patterns in the zebrafish ear are shown in Fig. 3A.
In amniotes, the exquisite spatial organization of hair cells along the auditory epithelium is critical for the discrimination of auditory stimuli at different frequencies. This is particularly advanced in the mammalian cochlea, where orderly rows of hair cells are organized in a tonotopic array in the organ of Corti. One row of inner hair cells and three rows of outer hair cells run along the cochlear duct from the base (high frequency detection) to the apex (low frequency detection) (reviewed in Raphael and Altschuler (2003) ; Fig. 3C). Vibration of the basilar membrane, amplified by the outer hair cells, determines a specific position where sound vibration peaks (reviewed in Dallos et al. (2006), Dallos (2008)). It is the inner hair cells that convert this sound energy into an electrical signal: mechanical stimulation of the inner hair cells by their movement relative to the tectorial membrane results in depolarization and stimulation of afferent neurons of the spiral ganglion. In general, short stereociliary bundles are associated with high frequency detection, while long stereociliary bundles are associated with low frequency detection.
Birds have two types of hair cells in the basilar papilla, tall and short hair cells (Fischer, 1994). The tall hair cells are the equivalent of the inner hair cells in mammals, and are innervated by both afferent and efferent fibers. The short hair cells, by contrast, have no afferent innervation at all, but receive efferent input. It is possible that they have a modulatory role, but no evidence exits to date for this (reviewed in Köppl( 2011)). A similar pattern is observed in the basilar papilla of lizards (Chiappe et al., 2007;Manley, 2011).
Distinct signals mediate differentiation of the lateral outer hair cell compartment versus the medial inner hair cell compartment of the developing cochlea, with evidence implicating Emx2, Delta-Notch and FGF signaling in this process. For example, Emx2 null mutant mice have about 60% fewer hair cells than their wild-type littermates; the remaining hair cells label positive for Myo7 and Fgf8, two inner hair cell markers. Outer hair cells are completely lost, leading to the idea that Emx2 may regulate the balance between proliferation and differentiation in hair cell progenitors (Holley et al., 2010). Conditional loss of Jag1 in the cochlea shifts the balance between outer and inner hair cells in favor of inner hair cells, consistent with the interpretation that Jag1 expands the prosensory state in the sensory epithelium via lateral induction; in addition, it regulates cell cycle exit via the expression of p27 Kip1 (Brooker et al., 2006;Kiernan et al., 2006). FGF signaling is also important for hair cell development; Fgf20 is required in the lateral part of the cochlea, and Fgf20 null mice are deaf and lack outer hair cells (Huh et al., 2012). After conditional loss of Fgfr1, hair cell precursors are reduced and preferentially differentiate into inner hair cells and pillar cells (Pirvola et al., 2002).
Mutations in Srrm4 (Deol, 1981;Whitlon et al., 1996;Nakano et al., 2012) and in a 'self-terminating' conditional Atoh1 allele  both predominantly lose inner hair cells. It has been proposed that Srrm4 might act downstream of Atoh1 in a feedback loop (Nakano et al., 2012). At later developmental stages, Atoh1 is expressed in inner hair cells earlier and at higher levels compared to outer hair cells and recent evidence indicates that prolonged expression is required for the correct hair cell differentiation, and that inner hair cells critically depend on Atoh1 for maintenance .

Neurons of the VIIIth ganglion
Different types of afferent ganglion neurons innervate the sensory hair cells of the vestibular and auditory systems. In the vestibular system, afferent fibers ending in both bouton-and calyx-type synapses are found, depending on the species (Wersäll, 1956;Goldberg et al., 1990) (Fig. 3B). In mammals, most afferents are dimorphic, terminating in both bouton and calyceal endings, and contacting both Type I and Type II vestibular hair cells Lysakowski et al., 1995). In the auditory system of mammals, there are two types of spiral ganglion cells, Type 1 and Type 2, both of which have bouton-type endings. Type 1 spiral ganglion cells contact inner hair cells and are large, bipolar cells that make up 90-95% of all the neurons in the spiral ganglion, in line with inner hair cells being the sensory receptor in the cochlea. Inner hair cells contact afferent endings from Type 1 ganglion cells at specialized ribbon synapses. Type 2 spiral ganglion cells contact outer hair cells and are small, bipolar or pseudomonopolar, and are less myelinated than Type 1 ganglion cells. Ribbon synapses with Type 2 cells occur, but only in the apical turn of the cochlea (reviewed in Raphael and Altschuler (2003), Nayagam et al. (2011), Bulankina and Moser (2012)).

Neurodegeneration and regeneration
The sensory cells in the inner ear and nose in mammals differ greatly in their regenerative potential. The OSNs of the nose are routinely replaced throughout life. The average life span of a murine OSN is 90 days (Mackay-Sim and Kittel, 1991), but these cells may survive up to a year (Hinds et al., 1984). By contrast, no epithelial maintenance has been described for the hair cells of the cochlea of mammals, though hair cell addition and repair occurs in lower vertebrates (reviewed in , Rubel et al.(2013)).
Whereas the OSNs are exposed to the outside world and regularly damaged, the hair cells of the inner ear are in a relatively protected environment. Nevertheless, sensory hair cells of the ear are lost through aging, and are also sensitive to damage from both noise and chemical exposure. Examples of hair cell-damaging drugs (ototoxins) include the aminoglycoside antibiotics, which are effective in the treatment of life-threatening infections, but can leave a patient deaf as a result. In mammals, lost auditory hair cells are not replaced; the reasons for this lack of regenerative potential are not fully understood. Often, once hair cells are damaged, the neurons of the VIIIth ganglion lose afferents and also undergo cell death with time (Webster and Webster, 1981;Schuknecht and Gacek, 1993).

Regeneration in the adult olfactory system
The loss of the sense of smell-anosmia-can significantly impair quality of life and is often associated with trauma or neurodegenerative disease such as Parkinson's or Alzheimer's disease, in addition to normal aging (Doty et al., 1984;Doty, 2012). This sensory deterioration is all the more striking given the well-documented self-renewal of the olfactory epithelium throughout adulthood in healthy individuals. OSNs have the remarkable ability to regenerate in adult organisms, including in humans, and the basally located and horizontal basal cells are thought to be the predominant and likely sole source of all cell types in the regenerating olfactory epithelium post-injury (Graziadei and Graziadei, 1979;Leung et al., 2007;Iwai et  2008; Bermingham-McDonogh and Reh, 2011). Intriguingly, a recent study in mice using P0-Cre-based fate mapping has suggested that as the olfactory epithelium matures, placode-derived basal cells are slowly replaced by neural crest-derived basal cells (Suzuki et al., 2013). As the use of Cre-based fate mapping of neural crest is often fraught with non-neural crest-specific labeling, confirmatory studies will be needed to determine the validity of this striking finding.
The transcription factor p63 has been implicated in maintenance of the horizontal basal cell population in the adult olfactory epithelium, and both expression and mutant studies suggest that its down-regulation may play an important role in the differentiation of these cells in adults (Fletcher et al., 2011;Packard et al., 2011). In addition, retinoic acid signaling is critical for progenitor cell maintenance as well as for neurogenesis in the olfactory epithelium (Peluso et al., 2012;Paschaki et al., 2013). Indicating possible crosstalk between varied cell types, a report by Jia and colleagues suggests that inositol triphosphate receptor subtype 3-and neurotrophic factor neuropeptide Y-expressing microvillous cells play an essential role in olfactory neuron regeneration postsimulated injury (Jia et al., 2013).
After damage, supporting cells in the basilar papilla re-enter the cell cycle and eventually differentiate into supporting cells and hair cells in both neonatal chicken and adult birds (Corwin and Cotanche, 1988;Ryals and Rubel, 1988;Hashino et al., 1992;Raphael, 1992;Stone and Cotanche, 1994;Warchol and Corwin, 1996;Stone et al., 1999). In addition, there is direct transdifferentiation of supporting cells and subsequent compensatory proliferation in amphibian sacculi and avian basilar papillae in response to damage (Adler and Raphael, 1996;Baird et al., 1996;Adler et al., 1997;Steyger et al., 1997;Baird et al., 2000;Roberson et al., 2004). Accordingly, Atoh1a is expressed in supporting cells shortly after hair cell damage (Cafaro et al., 2007;Lewis et al., 2012). Whereas direct transdifferentiation occurs within a matter of hours, it takes days for hair cells to arise from mitotic division of supporting cells, which eventually comprise 50-70% of the regenerated hair cells (Roberson et al., 2004;Cafaro et al., 2007). These data suggest that direct transdifferentiation is a fast way to replace hair cells, while cell cycle re-entry is slower, but better suited to replace large numbers of hair cells (Stone and Cotanche, 2007). Similarly, in the lateral line of fish and amphibians, supporting cells have been shown to replace damaged hair cells (Balak et al., 1990;Ma et al., 2008) and hair cell regeneration by both transdifferentiation and proliferation has been suggested in the adult zebrafish inner ear (Schuck and Smith, 2009;Sun et al., 2011;Liang et al., 2012).
In birds, regenerative proliferation is likely to depend on chromatin modification, as inhibitors of histone deacetylation have been shown to prevent cell cycle entry and thus diminish regenerative proliferation (Slattery et al., 2009). In addition, screens to identify transcription factors expressed differentially during avian hair cell regeneration have shed light on potential signaling pathways involved in regeneration (Hawkins et al., 2007) and their role in regenerative proliferation (Alvarado et al., 2011).
Two major differences have emerged between supporting cells in the basilar papilla in birds and their counterparts in the mammalian cochlea. After damage in birds, but not mammals (Shailam et al., 1999;Batts et al., 2009), Atoh1 expression is detectable in actively dividing supporting cells in the basilar papilla (Cafaro et al., 2007). Misexpression of Atoh1 in the inner ear of developing or mature mammals induces hair cell characteristics in these cells (Zheng and Gao, 2000;Kawamoto et al., 2003;Shou et al., 2003;Izumikawa et al., 2005;Staecker et al., 2007), but this potential is lost with age (Kelly et al., 2012;Liu et al., 2012). Thus regulatory events upstream of Atoh1 or modifications on the level of the Atoh1 promoter/chromatin structure may have altered mammalian otic sensory epithelia.
Another striking observation is that mammalian supporting cells have a decreased capacity for shape change (Forge, 1985;Cotanche, 1987). In the basilar papilla in birds, cell shape changes occur before cell cycle re-entry and cells adopt mature shapes once they differentiate into hair cells or support cells (Corwin and Cotanche, 1988;Marsh et al., 1990). This ability to undergo shape changes may be a requirement for regeneration. As mammalian supporting cells age, thick F-actin/E-cadherin belts are established in the apical junctions between supporting cells (Burns et al., 2008;Collado et al., 2011). By contrast, the supporting cells in chick, bony and cartilaginous fish, amphibians and turtles all have thin actin belts similar to those developing and neonate mice . However, it is currently unclear if this is permissive for regeneration or simply an interesting correlation. To date, the best approach for hair cell regeneration in zebrafish, and to a lesser extent in adult mammalian sensory epithelia, relies on Notch inhibition (Ma et al., 2008;Lin et al., 2011b;Mizutari et al., 2013).
Re-innervation has been reported in several damage models, but is not necessarily correlated with functional recovery and depends on the severity of the induced damage (Johnsson and Hawkins, 1972;Terayama et al., 1977;Terayama et al., 1979;Webster and Webster, 1982;Bohne and Harding, 1992;Strominger et al., 1995;Lawner et al., 1997). In mouse and guinea pig models of neuronal hearing loss, no evidence for regenerated fibers and newly formed synapses was found (Kujawa and Liberman, 2009;Lin et al., 2011a;Yuan et al., in press). Re-innervation (Martinez-Monedero et al., 2006) and synapse regeneration has recently been reported in a rat and mouse in vitro model (Wang and Green, 2011;Tong et al., 2013) and addition of Neurotrophin-3, BDNF or block of the repulsive guidance molecule RGMa increased synapse formation (Wang and Green, 2011;Brugeaud et al., 2013;Tong et al., 2013). Many advances have been made in trying to replace lost auditory neurons. Both inner ear cells and cells from other sources have successfully been stimulated in vitro to differentiate into neuronal cells (Li et al., 2003;Oshima et al., 2007) and to innervate hair cells in vitro Shi et al., 2007;Martinez-Monedero et al., 2008;Matsumoto et al., 2008) and in vivo (Hu et al., 2005;Okano et al., 2005;Corrales et al., 2006;Coleman et al., 2007). Most promisingly, some functional recovery has been reported in a deafened gerbil model following transplantation of human embryonic stem cellderived auditory neurons .

Conclusion
Continued assembly of the molecular cascades responsible for neurogenesis in the olfactory and otic systems has yielded regulatory networks that are increasingly elaborate in scope and complexity. Knowledge and understanding of such networks is already driving forward progress towards the development of cellbased therapies for sensory disorders such as deafness. The recapitulation of otic development in three-dimensional culture from mouse embryonic stem cells, for example, is an exciting step forward (Koehler et al., 2013). Likewise, in the olfactory system, recognition of the regenerative potential of the neural crestderived olfactory ensheathing glia has implications for the development of patient-based cell therapies for sensory and other disorders (Barraud et al., 2010).
More work remains to understand and reconcile the differences in otic and olfactory neurogenesis across various model systems. In addition, there is still much to learn about the timing and cellular interactions that allow system-wide organ development to proceed smoothly and precisely. A critical next step is to integrate our knowledge of signaling cascades with the complex, fourdimensional physical morphogenesis that occurs in the developing ear and nose during both development and regeneration. For example, our knowledge of mRNA expression and secreted protein gradients has grown rapidly, but these datasets often contain most of their information in just two dimensions. With the advent of increasingly powerful imaging technologies, it has become feasible to visualize protein expression, movement and interactions in vivo in the context of the cell-cell interactions that underlie organ morphogenesis and growth. Going forward, it will be exciting to map well-described molecular information onto this 'developing' spatiotemporal map of otic and olfactory morphogenesis more robustly and thus gain new, powerful insights into development and regeneration. Such four-dimensional mapping holds the promise of providing information useful for therapeutic purposes in the human ear and nose. Importantly, a greater general knowledge of neurogenesis will aid in promoting neuronal regeneration and repair both within and outside the otic and olfactory systems.