Endothelial Progenitor Cells and Vascular Alterations in Alzheimer’s Disease
Antía Custodia1 
Alberto Ouro1* 
Daniel Romaus-Sanjurjo1 
Juan Manuel Pías-Peleteiro1 
Helga E. de Vries2 
José Castillo3 
Tomás Sobrino1*
- 1NeuroAging Group (NEURAL), Clinical Neurosciences Research Laboratory (LINC), Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain
- 2Neuroimmunology Research Group, Department of Molecular Cell Biology and Immunology, Amsterdam Neuroscience, Amsterdam UMC, Amsterdam, Netherlands
- 3Neuroimaging and Biotechnology Laboratory (NOBEL), Clinical Neurosciences Research Laboratory (LINC), Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain
Alzheimer’s disease (AD) is a neurodegenerative disease representing the most common type of dementia worldwide. The early diagnosis of AD is very difficult to achieve due to its complexity and the practically unknown etiology. Therefore, this is one of the greatest challenges in the field in order to develop an accurate therapy. Within the different etiological hypotheses proposed for AD, we will focus on the two-hit vascular hypothesis and vascular alterations occurring in the disease. According to this hypothesis, the accumulation of β-amyloid protein in the brain starts as a consequence of damage in the cerebral vasculature. Given that there are several vascular and angiogenic alterations in AD, and that endothelial progenitor cells (EPCs) play a key role in endothelial repair processes, the study of EPCs in AD may be relevant to the disease etiology and perhaps a biomarker and/or therapeutic target. This review focuses on the involvement of endothelial dysfunction in the onset and progression of AD with special emphasis on EPCs as a biomarker and potential therapeutic target.
Introduction
Alzheimer’s disease (AD) is the main neurodegenerative disease leading to dementia and cognitive impairment. According to World Alzheimer Report 2019: Attitudes to dementia there are 50 million people with dementia (two-thirds with AD), with an expected increase of more than 152 million patients by the year 2050 (International, 2019).
Alzheimer’s disease can be classified according to its onset. Early-onset AD, which is mostly caused by autosomal dominant mutations; and late-onset AD, which accounts for most cases and whose etiology remains unclear. The most studied mutations responsible for autosomal dominant AD occur in the β-amyloid (Aβ) precursor protein (APP), presenilin 1 (PS1), and presenilin 2 (PS2) genes. However, those mutations collectively represent less than 1% of total cases. Late-onset AD is diagnosed from the age of 65 onward, and it has a multifactorial cause in which both environmental and genetic risk factors are involved (Giri et al., 2017). Among, different vascular-associated genetic risk factors, those corresponding to ε4 allele of APOE (APOE ε4), phatidylinositol binding clathrin assembly protein (PICALM), clusterin (CLU) or sortilin related receptor-1 (SORL1) genes have been identified in AD (Sweeney et al., 2019). From all of them, APOEε4 is the most studied. Curiously, all affect Aβ clearance across the blood-brain barrier (BBB) (Sweeney et al., 2019).
Due to the symptomatic complexity of the disease and its similarity with other types of dementia, an accurate premortem diagnosis of AD is particularly challenging. Regrettably, the definitive diagnosis is made by postmortem brain tissue histological tests. Currently, techniques such as magnetic resonance imaging (MRI) (Wolz et al., 2011; Bron et al., 2017), positron emission tomography (PET) (Salmon et al., 1994; Ding et al., 2019), and detection of biomarkers released into the cerebrospinal fluid (CSF) (Blennow et al., 2001; Khoonsari et al., 2019), are only able to detect AD patients in late stages of the disease. Furthermore, different techniques have been recently developed to detect mild cognitive impairment (MCI) biomarkers (a stage prior to AD), including the analysis of hippocampal BBB leakage by dynamic contrast-enhanced MRI Ktrans values (Montagne et al., 2015, 2020; Nation et al., 2019) and the analysis of platelet-derived growth factor receptor-β (sPDGFRβ) levels in CSF, a marker of pericyte damage (Montagne et al., 2015; Nation et al., 2019). However, none of these techniques became the gold standard in clinical practice for the early diagnosis of AD.
Currently, there are different hypotheses about the AD onset:
(a) β-amyloid deposit and hyperphosphorylated tau protein hypothesis: AD is originated from the presence of extraneuronal amyloid plaques formed by amyloid fibers composed of Aβ protein, and intraneuronal neurofibrillary tangles (NFTs), that are mainly formed by paired helical filaments (PHF) of the hyperphosphorylated tau protein (Gallardo and Holtzman, 2019; Paroni et al., 2019; Arnsten et al., 2021).
(b) Cholinergic hypothesis: the cause of AD is due to alterations of the cholinergic system. In AD there are modifications in cholinergic transport, acetylcholine release, expression of cholinergic receptors, reduction of acetylcholine transferase activity, and loss of cholinergic neurons. These events are relevant for AD since the cholinergic system is closely related to memory (Mufson et al., 2008; Hampel et al., 2018).
(c) Two-hit vascular hypothesis: a damage in cerebral vasculature (hit one) induces the accumulation of Aβ in the brain (hit two) (Zlokovic, 2011). (See below section “Two-hit vascular hypothesis” for more information.) Several studies support the early appearance of vascular alterations in AD (Sweeney et al., 2018; Apátiga-Pérez et al., 2021; Hussain et al., 2021; Kurz et al., 2021). In this scenario, endothelial progenitor cells (EPCs) appear as a possible therapeutic target by considering their involvement in the maintenance of vasculature.
For all the aforementioned, this mini-review is focused on vascular and angiogenic alterations in AD, besides the potential key role of EPCs on the AD’s etiology, and their potential as a therapeutic biomarker.
Evidence of Vascular Alterations in Alzheimer’s Disease
The alteration and dysfunction of the cerebral vasculature is an important component of AD pathophysiology (Figure 1A shows a healthy capillary and Figure 1B shows an AD capillary). Hence, this process could contribute to the appearance and progression of the disease as well as promote neurodegeneration, inflammation, Aβ accumulation, and tau phosphorylation (Sagare et al., 2012). Several findings acquired by neuroimaging techniques, analysis of postmortem brain samples, and CSF biomarkers detection support a vascular dysfunction in AD (Montagne et al., 2017; Sweeney et al., 2018).
Figure 1. (A) Healthy capillary; the BBB has tight junctions between endothelial cells, pericytes enveloping endothelial cells, astrocytes, and normal blood flow. (B) AD capillary; Main vascular alterations occurring in AD: (1) the rupture and dysfunction of the BBB increase the permeability of different cells and molecules; (2) the accumulation of erythrocytes in the parenchyma generates neurotoxic products (Fe2+) that damage brain cells through the production of ROS; (3) the extravasation and consequent accumulation of neurotoxic molecules induces neurodegeneration and vascular damage; (4) oligemia induces a reduction in nutrient and oxygen supply, (5) generating hypoxic zones increases Aβ production and tau phosphorylation; (6) Aβ flow through the BBB is impaired due to a lower expression of LRP-1 and a higher expression of RAGE, leading to Aβ accumulation in the brain parenchyma; (7) blood vessels release a large amount of proinflammatory mediators (NO, TNFα, and IL-6) that together with (8) the extravasation of immune system cells generate inflammation. All together finally generate neuronal damage. ROS, reactive oxygen species; Ig, immunoglobulins; BBB, blood-brain barrier; Aβ, amyloid β protein; LRP-1, low-density lipoprotein receptor-related protein 1, RAGE, receptor for advanced glycation end products; NO, nitric oxide; TNF-α, tumor necrosis factor-alpha; IL-6, interleukin-6, HIF-1α, hypoxia-induced factor 1α; MAPK, mitogen-activated protein kinase. (C) Role of EPCs in vascular maintenance/repair e-EPCs participate in vasculogenesis and/or angiogenesis in a paracrine manner through the release of proangiogenic factors. L-EPCs participate by directly differentiating into mature endothelial cells. Created with BioRender.com.
Neuroimaging studies using 18F-fluorodeoxyglucose (FDG)-PET linked alterations in glucose transport to MCI and early AD. This was determined through a reduction in glucose transporter-1 (GLUT-1) in the BBB (Minoshima et al., 1997; Bailly et al., 2015; Nelson et al., 2016). P-glycoprotein (P-gp) is a membrane protein found in the endothelial cells of the BBB. Of interest, its principal function is to eliminate xenobiotics from cerebral parenchyma to the blood, although, it can also transport Aβ (Gil-Martins et al., 2020). Importantly, 11C-verapamil-PET studies described the dysfunction of P-gp in AD and MCI patients (Van Assema et al., 2012; Deo et al., 2014). Additionally, MRI approaches showed that early AD patients present BBB leakage in the gray matter and cortex, which is associated with cognitive impairment and a decreased cerebral blood flow in gray matter (Van De Haar et al., 2016a,b). Interestingly, the hippocampal BBB leakage occurs before suffering brain atrophy or dementia in MCI patients and APOEε4 carriers, in addition, it is regardless of Aβ and tau changes (Montagne et al., 2015, 2020; Nation et al., 2019). MRI also revealed the presence of microbleeds in the central nervous system in 45–78 and 25% of patients at the initial stages of AD (before developing dementia) or with MCI, respectively (Brundel et al., 2012; Uetani et al., 2013; Yates et al., 2014). These results agree with the hypothesis of an early endothelial dysfunction underlying the onset of AD.
Blood-brain barrier permeability was also determined in postmortem tissue (Figure 1B), where the leakage of certain substances (e.g., fibrinogen, fibrin, thrombin, plasmin, albumin, or immunoglobulins) from capillaries and the subsequent accumulation in the parenchyma was detected (Wisniewski and Kozlowski, 1982; Grammas et al., 2006; Ryu and McLarnon, 2009; Sengillo et al., 2013). Additionally, the extravasation of erythrocytes, peripheral macrophages, and neutrophils has been observed (Fiala et al., 2002; Cullen et al., 2005; Zenaro et al., 2015). Electron microscopy and immunostaining techniques have determined the degeneration of pericytes, considered key cells in the maintenance of the BBB (Baloyannis and Baloyannis, 2012; Sengillo et al., 2013). In this regard, an increase in sPDGFRβ levels, a marker of pericyte damage, was found in the CSF of both AD and MCI patients (Montagne et al., 2015; Miners et al., 2019; Nation et al., 2019). Elevated levels of sPDGFRβ correlate with the CSF/plasma albumin ratio and the levels of fibrinogen in CSF, both are markers of BBB leakage (Miners et al., 2019; Nation et al., 2019). In this sense, the existence of endothelial degeneration in AD patients and reduction in the length of the capillaries has been confirmed, as well as the reduced expression of tight junction proteins in capillaries (Baloyannis and Baloyannis, 2012; Halliday et al., 2016). Remarkably, several molecular changes have been also observed in the cerebral endothelium of AD patients, such as low expression of low-density lipoprotein receptor-related protein 1 (LRP-1) and GLUT-1 (Mooradian et al., 1997; Donahue et al., 2006), which validate previous neuroimaging studies. Curiously, LRP-1 removes Aβ from the brain in conjunction with P-gp (Storck et al., 2018). Moreover, other molecular changes including increased levels of the receptor for advanced glycation end products (RAGE) have been reported (Donahue et al., 2006). Interestingly, RAGE induces the uptake of circulatory Aβ to the cerebral parenchyma (Donahue et al., 2006). Cyclophilin A (CypA) and matrix metalloproteinase-9 (MMP-9) are also overexpressed, leading to the degradation of the BBB tight junctions (Halliday et al., 2016). APOEε4 increases the damage of the BBB by the activation of the cyclophilin-A-MMP-9 pathway (Bell et al., 2012; Halliday et al., 2013). Accordingly, APOEε4 carriers have elevated levels of CypA, MMP9, and sPDGFRβ in the CSF (Montagne et al., 2020). In microvessels isolated from AD brains higher levels of inflammatory mediators were determined, such as nitric oxide (NO), tumor necrosis factor-alpha (TNF-α), and interleukin-6, and 8 (IL-6 and IL-8), MMPs, prostaglandins, and leukocyte adhesion molecules, compared with healthy controls (Dorheim et al., 1994; Grammas and Ovase, 2001; Thirumangalakudi et al., 2006). Interestingly, some of these molecules are implicated in angiogenesis (Grammas and Ovase, 2001; Grammas et al., 2006).
Alterations in angiogenesis also occur in AD (Steinman et al., 2021). Vascular dysregulation leads to a lack of oxygen in the brain (hypoxia), which eventually induces an up-regulation of pro-angiogenic proteins in brain vessels, such as vascular endothelial growth factor (VEGF), thrombin, or hypoxia-induced factor 1α (HIF-1α), among others (Grammas et al., 2006; Thirumangalakudi et al., 2006). Despite the increase in pro-angiogenic factors, there is no evidence of increased vascularization. Indeed, it has been shown that vascular density decreases (Baloyannis and Baloyannis, 2012). Although the causes underlying abnormal angiogenesis are not clear, in vitro and in vivo studies revealed that the Aβ peptide has anti-angiogenic effects (Paris et al., 2004). Accordingly, brain endothelial cells from AD patients have low levels of vascular-restricted mesenchyme homeobox 2 gene (MEOX-2). MEOX-2 acts as a regulator for the proliferation of vascular cells. Low levels of the mentioned gene in AD generate aberrant angiogenesis that results in a decrease in cerebral microcirculation. In animal models, MEOX-2 deletion reduces LRP-1 levels, leading to decreased Aβ efflux from the brain parenchyma to the blood, among other vascular alterations (Wu et al., 2005). Importantly, a hypoxic environment suppresses the expression of MEOX-2 (Xia S. et al., 2012).
In summary, there is a large amount of evidence, from multiple approaches, that support the existence of a neurovascular component in the onset of AD. Remarkably, this vascular dysfunction starts before developing atrophy and/or dementia and continuous in later stages. Based on this evidence, the two-hit vascular hypothesis was proposed (Zlokovic, 2011).
Two-Hit Vascular Hypothesis
Zlokovic (2005) suggested that neurovascular dysfunction contributes to the cognitive decline and neurodegeneration associated to AD. Later, his group proposed the two-hit vascular hypothesis, where damage in cerebral vasculature (hit one) induces the accumulation of Aβ in the brain (hit two) (Zlokovic, 2011).
The damage in the cerebral vasculature (hit one) can be caused by either several vascular risk factors (such as hypertension, diabetes, hypercholesterolemia, or smoking, among others), or by genetic risk factors like APOEε4. The cerebral vasculature undergoes several outcomes during the injury (Figure 1B). Accordingly, the cerebral blood flow is reduced (oligemia), leading to hypoxia in some areas, and the subsequent release of reactive oxygen species (ROS) that promote cellular damage by oxidative stress (Carvalho et al., 2009), as well as inducing the expression of HIF-1α. In addition, HIF-1α. increases the expression and activity of β-secretase and the activity of γ-secretase. Therefore, this raises the amyloidogenic pathway and ultimately Aβ production (Zhang et al., 2007; Li et al., 2009). There is also a dysfunction in the BBB, leading to an increase in the permeability of toxic molecules and their accumulation in the brain parenchyma (mentioned in the previous section). Some of these molecules cause neurodegeneration and further increase the damage to the cerebral vasculature (Chen and Strickland, 1997; Mhatre et al., 2004; Paul et al., 2007; Chen et al., 2010). Moreover, the presence of erythrocytes in the parenchyma generates neurotoxic products, such as iron, leading to an increase of ROS and therefore, brain damage (Regan and Guo, 1998).
Finally, the cerebrovascular dysfunction triggers inflammation, defective Aβ clearance in the brain, and increased influx of peripheral Aβ through BBB (Figure 1B). Likewise, tau hyperphosphorylation is also promoted by these harmful processes leading to the formation of NFTs (Busciglio et al., 1995; Gordon-Krajcer et al., 2007; Fang et al., 2010; Koike et al., 2010; Lee D. et al., 2010). All these events result in the accumulation of Aβ and tau in the brain tissue and Aβ around cerebral blood vessels (hit two) (Sagare et al., 2012; Nelson et al., 2016; Sweeney et al., 2018). In fact, it has recently been described that insoluble vascular amyloid deposits could induce BBB disruption (Soto-Rojas et al., 2021). In summary, the two-hit vascular hypothesis suggests that the accumulation and hyperphosphorylation of tau are secondary to a vascular lesion and/or a lesion generated by Aβ (Grammas, 2011; Zlokovic, 2011). Moreover, there is a feedback between the cerebrovascular dysfunction and inflammation, since each one can induce the other (Clapp et al., 2004; Theofilis et al., 2021). Indeed, one of the risk factors for AD is chronic inflammation (Tao et al., 2018).
Overall, these events promote synaptic dysfunction, neuronal damage, neurodegenerative change, and finally neuronal death, thus generating dementia (Chen and Strickland, 1997; Regan and Guo, 1998; Grammas et al., 2000; Mhatre et al., 2004; Carvalho et al., 2009; Chen et al., 2010; Feuillette et al., 2010; Tian et al., 2013; Pereira et al., 2021).
Endothelial Progenitor Cells and Their Potential Role in Alzheimer’s Disease
Since angiogenesis and the integrity of the BBB are both crucial for the development of AD, and EPCs are essentials in endothelial repair processes, it is tempting to propose that EPCs may have a key role in this disease. In recent years, our group has described that EPCs are involved in other neurovascular diseases such as stroke and migraine (Sobrino et al., 2007, 2011, 2012a,b; Rodríguez-Osorio et al., 2012; Rodríguez et al., 2016; Pías-Peleteiro et al., 2017).
Endothelial progenitor cells constitute a subtype of cells present in the blood that derive mostly from the bone marrow. These cells exhibit characteristics of both endothelial and stem cells since they can differentiate into mature endothelial cells and self-renew, respectively (Hristov et al., 2003; Yoder, 2012). Three surface markers are characteristics of EPCs: CD34, VEGF receptor 2 (VEGFR-2), and CD133. CD34 is a marker expressed by hematopoietic stem cells and certain types of mature endothelial cells. VEGFR-2 is a specific receptor of VEGF and is expressed in endothelial cells and uncommitted stem cells. CD133 is an early marker of hematopoietic stem cells (Hristov et al., 2003). EPCs participate in the maintenance of the endothelium by acting as a cellular reservoir for the replacement of dysfunctional endothelial cells or by releasing angiogenic growth factors (Figure 1C; Hristov et al., 2003; Lee et al., 2009; Malinovskaya et al., 2016). There are two different types of EPCs: (a) early-outgrowth EPCs (e-EPCs), circulatory angiogenic cells, or colony-forming unit endothelial cells (CFU-EC) which participate in both the process of network formation and the repair of injured endothelial cells in a paracrine way by secreting different angiogenic factors; and (b) late-outgrowth EPCs (l-EPCs), endothelial outgrowth cells, or endothelial colony-forming cells, which improve angiogenesis by differentiating into mature endothelial cells (Hur et al., 2004; Bauman et al., 2018). In addition to their functionality, both types of EPCs can be recognized by characterization in vitro. Whereas e-EPCs appear after a few days in culture and form colonies with spindle-shaped cells around them, l-EPCs appear after 2–3 weeks in culture and present a cobblestone shape (Hur et al., 2004).
The number of EPCs has been proposed as a possible surrogate marker of vascular function, and low EPCs counts are associated with higher cardiovascular risk (Hill et al., 2009; Bitterli et al., 2016; Hayek et al., 2016). These cells have also been implicated in the maintenance of cerebral endothelial vasoreactivity in healthy subjects (Chung et al., 2015). EPCs may have an important role in different nervous system diseases. For example, EPCs attach to the endothelium and promote the formation of new vessels after an ischemia and/or hypoxia event. Consequently, EPCs induce and modulate vasculogenesis and angiogenesis in those hypoxic areas, as well as stimulate re-endothelialization of injured vessels (Yoder, 2012). Indeed, high EPCs levels have been associated with a good functional and neurological prognosis, besides a reduction of the infarct growth in patients with ischemic stroke (Sobrino et al., 2007). In addition, the EPCs percentage in blood was associated with serum levels of VEGF, stromal cell-derived factor-1α and, active MMP-9 (Sobrino et al., 2012b). Interestingly, patients treated with statins had larger EPCs levels and, therefore, a better outcome (Sobrino et al., 2012a). This relationship has also been established in intracerebral hemorrhage (ICH) patients (Sobrino et al., 2011; Pías-Peleteiro et al., 2017). Notably, ICH patients who presented the Pro72 single-nucleotide polymorphism in the tumoral protein 53 (Tp53) gene had higher levels of circulating EPCs, EPCs-mobilizing cytokines, and, eventually, better functional outcome (Rodríguez et al., 2016). These factors were related to greater neovascularization. Likewise, a reduced number of EPCs has been shown in patients with migraines, especially during attacks (Rodríguez-Osorio et al., 2012). Recently, a relationship has been observed between the elevated levels of EPCs and cerebral small vessel disease burden, which is a risk factor for the development of AD (Kapoor et al., 2021). Curiously, sickle cell anemia (SCA) patients, a monogenic disease that affect erythrocyte membranes, present a high risk to develop a small vessels disease such as ischemic, hemorrhagic, and silent strokes (Ito et al., 2020). Newly, genetic alterations in l-EPCs of genes involved in angiogenesis, coagulation, inflammation, apoptosis, and cell adhesion have been observed in SCA patients that suffered a stroke (Ito et al., 2020). Therefore, EPCs seem to be involved in cerebrovascular diseases.
Several studies have analyzed the number of circulating EPCs in AD patients and their ability to form CFU-EC colonies (Table 1). However, there are discrepancies in these results. Lee and co-workers determined that AD patients did not present significant differences in the number of circulating EPCs compared with subjects without AD who present cardiovascular risk factors. Despite that, AD patients had a significant reduction in CFU-EC colony formation, and this decrease was correlated with a greater cognitive impairment (Lee et al., 2009). In accordance with some of these findings, other works concluded that there are no significant differences in the number of circulating EPCs in AD patients and controls (Breining et al., 2016; Haiyuan et al., 2020). However, EPCs from moderate and severe AD showed functional alterations in culture, such as reduced adhesion and migration capacity, compared to mild AD and controls (Haiyuan et al., 2020). Conversely, a clinical study indicated that AD patients had a reduced number of circulating EPCs compared with control subjects and that a lower number of EPCs correlates with greater cognitive impairment (Kong et al., 2011). The discrepancies in these studies may be due to the age of the subjects since the number of circulating EPCs decrease with age (Jie et al., 2009; Xia W. H. et al., 2012). In this regard, Breining et al. (2016) and Haiyuan et al. (2020) analyzed data from older subjects than Lee et al. (2009) and Kong et al. (2011). As a result, the physiological decrease in the number of EPCs with aging may mask the results. Furthermore, the difference in the results could also be due to the different inclusion and exclusion criteria used in the studies besides the likely existence of underlying diseases. Moreover, none of the studies differentiated between APOEε4 carriers, and both APOEε4 carriers and low levels of EPCs are considered cardiovascular risk factors (Hill et al., 2009; Mahley, 2016). Although the number of circulating EPCs is controversial, several studies reported functional alterations in EPCs (Lee et al., 2009; Haiyuan et al., 2020). In concordance with these results, another study in AD patients observed that e-EPCs presented reduced chemotaxis, and paracrine angiogenic properties, increased senescence; and altered gene expression (most of them related to physiological cellular processes) (Lee S. T. et al., 2010). Other factors involved in the pathogenesis of AD such as Aβ1–42 accumulation may also influence the functionality of e-EPCs. High concentrations of Aβ1–42 induce apoptosis, with AD-derived e-EPCs being more susceptible (Lee S. T. et al., 2010). Moreover, aging leads to functional alterations in e-EPCs that correlate with endothelial dysfunction (Heiss et al., 2005). Therefore, although the results are compromised, all the aforementioned studies analyzing EPCs in culture observe functional alterations of these cells in AD regardless of their circulating number.
Table 1. Summary of relevant preclinical and clinical studies on association between EPCs and AD.
Circulating progenitor cells (CPCs) are cells involved in tissue maintenance and repair (Sidney et al., 2014). Different authors have described CD34 as a marker for this cell lineage (Sidney et al., 2014). Within CPCs, different subpopulations of cells can be determined not only by the different markers expressed on their plasma membrane but also by the ability to differentiate into one or more mature cell types. EPCs represent one of these subpopulations (Sidney et al., 2014). Therefore, we have included different studies relating CPCs and AD in this mini-review, which shows some discrepancies in the results (Table 1). For example, there is a significant increase in circulating CD34+/CD133+ and CD34+ progenitor cells in moderate-severe AD compared to healthy subjects (Stellos et al., 2010) and CD34+ cells in early AD (Bigalke et al., 2011). In contrast, another study reported a reduction in the levels of CD34+ cells in early AD, and the number of these cells was inversely correlated with Aβ1–42 levels and Aβ42/40 ratio in CSF (Maler et al., 2006). Moreover, the number of CD34+ and CD34+/CD133+ cells in AD patients was inversely correlated with cognitive function and age (Stellos et al., 2010). Contrary, another study found that in patients with coronary artery disease, lower numbers of CPCs are associated with cognitive impairment (Moazzami et al., 2020). Regarding cognitive impairment, patients with MCI present reduced levels of circulating EPCs as well as CD34+/CD133+ and CD34+ progenitor cells (Nation et al., 2018). Concerning CD34+ cells, a lower number of these cells was associated with worse memory, lower posterior cingulate gyrus cortical thickness, and bilateral hippocampal hyperperfusion (Nation et al., 2018). However, the reduced number of studies and their controversial results highlight the need of further studies in order to reach more conclusive results about EPCs and CPCs in the onset and progression of AD.
Additionally to the analysis of the number of EPCs in AD, the therapeutic potential of these cells has also been suggested in different animal models (Table 1). For instance, e-EPCs were injected intravenously into repeated scopolamine (SCO)-induced cognitive impairment rats, an experimental model that replicates biomarkers of AD (Safar et al., 2016). As a result, there was an improvement in learning and memory; besides attenuation of Aβ plaque deposition, suppression of Aβ and p-tau levels, and reversal of neurotransmitter aberrations. L-EPCs were also injected intravenously in APP/PS1 transgenic mice, exhibiting an enhanced penetration of exogenous EPCs into the brain compared to controls (Yuan et al., 2016). Subsequently, using the same transgenic mice model, l-EPCs were injected directly into the hippocampus (Zhang et al., 2018). The transplantation of EPCs up-regulated tight junction proteins (such as zonula occludens-1, occludin and, claudin-5) in the BBB, increasing microvessels density and promoting angiogenesis in the hippocampus and cortex. The EPCs also exerted an anti-apoptotic effect promoting neuronal survival in the hippocampus. In addition, a reduction in the area and intensity of Aβ plaques in the hippocampus and cerebral cortex was observed. Moreover, learning and memory were significantly improved in AD mice (APP/PS1) after EPCs transplantation (for more details see Table 1). Therefore, the use of transfected EPCs has been proposed as a possible treatment pathway in AD by taking advantage of their ability to home to the damaged BBB. Recently, transfected EPCs that release antibodies against Aβ and reduce its aggregation have been generated (Heller et al., 2020). However, this novel therapeutic approach has not yet been tested in vivo. Although, in other neurological pathologies, such as traumatic brain injury, the intraventricular administration of l-EPCs resulted in greater integrity of the BBB and increased angiogenesis in a mouse model (Huang et al., 2013). In ischemic stroke, intra-arterial administration of l-EPCs resulted in reduced infarct volume, as well as increased angiogenesis and vascular density (Lin et al., 2020). Therefore, EPCs are postulated as a good therapeutic option for pathologies that present BBB alterations.
Discussion
Although AD is the main type of dementia worldwide, its etiology remains unclear. The Zlokovic two-hit vascular hypothesis proposes that AD starts from initial damage in the cerebral vasculature. Different studies in AD have demonstrated that there is a dysfunction of the BBB leading to hypoperfusion and hypoxia, accumulation of Aβ and hyperphosphorylation of tau, accumulation of neurotoxic molecules, and inflammation, among others in cerebral parenchyma. Altogether, these mechanisms cause neurodegeneration, neuronal dysfunction, an increase of pro-angiogenic molecules, and aberrant angiogenesis.
The basis of the decreased angiogenesis seen in AD remains unclear, although it has been proposed that it is due to either the accumulation of Aβ or the low expression of MEOX-2. However, the main cells responsible for carrying out angiogenesis in hypoxic sites are EPCs. Therefore, these cells could be involved in aberrant angiogenesis.
In the last years, clinical studies have analyzed the relationship between the number of EPCs and AD patients. The obtained data were contradictory since some studies did not observe significant differences in the number of EPCs, while others did. As discussed above, age and inclusion criteria may lead to observed differences. Interestingly, studies using animal models of AD showed that exogenous administration of EPCs improved learning, memory, and angiogenesis, attenuated Aβ deposition, reduced p-tau levels, and up-regulated the number of tight junctions, among others.
Taking all these data into account, we can conclude that there are several vascular and angiogenic alterations in AD and that EPCs may play a key role in endothelial and BBB dysfunction associated with AD. Moreover, in vivo studies using EPCs as a therapeutic approach open a possible new path for the treatment of AD. However, further studies are necessary to confirm the potential key role of EPCs as an early diagnostic and therapeutic biomarker in AD, and to elucidate the underlying mechanisms associated with the EPC’s therapeutic properties.
Author Contributions
JC and TS: conceptualization. AC, AO, DR-S, and JP-P: bibliographic study. JC, HV, and TS: supervision. AC, AO, and DR-S: writing – original draft. All authors contributed to writing – review and editing.
Funding
This study was partially supported by grants from the Xunta de Galicia (TS: IN607A2018/3, TS: IN607D 2020/09, AC: IN606A-2021/015, and DR-S: IN606B-2021/010), and Science Ministry of Spain (TS: RTI2018-102165-B-I00 and TS: RTC2019-007373-1). Furthermore, this study was also supported by grants from the INTERREG Atlantic Area (TS: EAPA_791/2018_ NEUROATLANTIC project), INTER-REG V A España Portugal (POCTEP) (TS: 0624_2IQBIONEURO_6_E), and the European Regional Development Fund (ERDF). Moreover, this work was financed by grants from Horizon 2020 #686009-PANA Project (TS and HV). Finally, TS (CPII17/00027) was recipient of a research contract from the Miguel Servet Program from the Instituto de Salud Carlos III. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: Alzheimer’s disease, biomarkers, blood brain barrier dysfunction, endothelial progenitor cells, endothelial repair, neurotoxicity, two-hit vascular hypothesis, vascular alteration
Citation: Custodia A, Ouro A, Romaus-Sanjurjo D, Pías-Peleteiro JM, de Vries HE, Castillo J and Sobrino T (2022) Endothelial Progenitor Cells and Vascular Alterations in Alzheimer’s Disease. Front. Aging Neurosci. 13:811210. doi: 10.3389/fnagi.2021.811210
Received: 08 November 2021; Accepted: 14 December 2021;
Published: 26 January 2022.
Edited by:
Zhen Zhao, University of Southern California, United StatesReviewed by:
Qiuying Zhao, University of Southern California, United StatesAxel Montagne, The University of Edinburgh, United Kingdom
Xinying Guo, University of Southern California, United States
Amy Renee Nelson, University of South Alabama, United States
Copyright © 2022 Custodia, Ouro, Romaus-Sanjurjo, Pías-Peleteiro, de Vries, Castillo and Sobrino. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Alberto Ouro, alberto.ouro.villasante@sergas.es; Tomás Sobrino, tomas.sobrino.moreiras@sergas.es