Role of scavenger receptors in glia-mediated neuroinflammatory response associated with Alzheimer's disease.

It is widely accepted that cells serving immune functions in the brain, namely, microglia and astrocytes, are important mediators of pathological phenomena observed in Alzheimer's disease. However, it is unknown how these cells initiate the response that results in cognitive impairment and neuronal degeneration. Here, we review the participation of the immune response mediated by glial cells in Alzheimer's disease and the role played by scavenger receptors in the development of this pathology, focusing on the relevance of class A scavenger receptor (SR-A) for A β clearance and inflammatory activation of glial cell, and as a potential target for Alzheimer's disease therapy.

1. Introduction

Alzheimer's disease (AD) is the most prevalent form of dementia, being usually diagnosed in people over 65 years, although the less prevalent early-onset forms of AD develop at earlier ages [1]. AD shows an increasing prevalence mainly due to the population aging. Dementia prevalence rises exponentially, doubling the rate of AD every 5 years after the age of 60 with a 15-fold prevalence increment from-age-60 to 85 years [2].

The pathophysiology of this dementia is characterized by the extracellular accumulation of amyloid-β (Aβ) and the intracellular formation of neurofibrillary tangles of the Tau protein in neurons, in association with neuronal dysfunction and cell death in some brain areas as the hippocampus. Although Aβ has been considered to be the main agent implicated in AD pathogenesis, it is still uncertain if Aβ plaques are causative for AD or a consequence of its pathological changes.

There are several hypotheses that attempt to explain the origin of AD [3], although the most popular is still the “Aβ cascade hypothesis” [4], which considers Aβ as the key pathogenic factor. The “inflammation hypothesis” [5] and the “glial dysfunction hypothesis” [6] have lately gained increased support. With some differences, both of them state that Aβ accumulation is a consequence of the dysregulated activation of glial cells, which in turn induce an inflammatory response, alter their Aβ-clearance activity, and mediate the neurotoxic effects of Aβ [7, 8].

2. Glial Dysfunction Hypothesis

It is widely known that aging, the most robust risk factor for AD, is also strongly associated with a progressive increment on the inflammatory state of the organism. Inflammation induces a large amount of cell changes at multiple levels, including microglial cells [9], and, as it will be discussed in the next section, microglial cells also become more neurotoxic in response to inflammatory states [10]. Whereas the inflammation hypothesis considers that hyperreactive microglia is the major contributor to the adverse events associated with AD, the glial dysfunction hypothesis suggests that impairment of normal glial functions, meaning qualitative changes, and not only quantitative changes on microglial cell activation, are responsible for the synaptic dysfunction and the neurodegenerative process observed in AD [6].

As it will be further discussed, glia are the scavenger cells of the brain. By having a reduced capability to clear Aβ [11], Aβ accumulates and microglial cells become activated and create a cytotoxic environment that induce a vicious circle that potentiates a neuroinflammatory state and neurotoxicity [12, 13]. Because the impairment of Aβ clearance induce the accumulation of the peptide even if there are no changes in Aβ production, this hypothesis states that Aβ accumulation would be a consequence and not a cause of the pathogenic changes leading to AD [14, 15].

3. Neuroinflammatory Response in AD

3.1. Microglial Cell Response

There is robust evidence showing high levels of inflammatory mediators in the brain of AD patients. Around senile plaques, a strong presence of TNF-α, IL-1β, IL-6, monocyte chemoattractant protein-1 (MCP-1), complement proteins as C1q, C1r, C2, C3, C4, C5, C6, C7, C8, and C9, C-reactive protein, and class II major histocompatibility complex antigen HLA-DR is observed [16-20]. When the effect of inflammatory cytokines over the production of Aβ was evaluated, it was demonstrated that exposure to cytokines such as IL-6 and IL-1, increase neuronal amyloid precursor protein (APP) mRNA expression [21]. In addition, glial cultures obtained from rapid brain autopsies of AD patients stimulated with Aβ show an increased release of prointerleukin-1β (pro-IL-1β), IL-6, IL-8, TNF-β, MCP-1, macrophage inflammatory peptide-1α (MIP-1α), and macrophage colony-stimulating factor (M-CSF) [22], corroborating the inflammatory activation of glial cells as part of the physiopathology of AD. Despite of this, in vitro studies have demonstrated that Aβ potentiates inflammatory activation of microglia [23], with different forms of Aβ showing distinct patterns of cytokine release; for instance, soluble forms of Aβ 1–40 stimulate specifically the release of IL-1β, while Aβ 1–42 induces the release of IL-1α and IFN-γ [24].

Also, immunohistochemical studies of the brain of AD patients have shown the presence of reactive microglia closely associated with senile plaques [20, 25]. The exposure of microglia to a soluble form of APP (sAPP) induces an increase of activation markers in microglia and enhances their production of neurotoxins [26]. More specifically, Aβ stimulates the NFκB-dependent pathway [27], which in turn induces the cytokines production by microglia and initiates the neurotoxic effects mediated by these cells [17].

Using mouse models of AD, Simard et al. showed that amyloid plaques are capable of chemoattracting immune cells from the bone marrow into the brain parenchyma, which adopt a microglial cell phenotype in the brain and suggested that these immigrant cells are the main responsible for Aβ plaque clearance [28]. Microglial cell-associated Aβ clearance was originally shown by incubating murine microglia with fluorescent-labeled Aβ [11]. The study also established the participation of scavenger receptors (SRs) in this process by demonstrating that coincubation with an excess of SRs ligands blocked the phagocytosis of Aβ. Also, the use of Chinese hamster ovary (CHO) cells transfected with scavenger receptors of class A (SR-A) and class B (SR-B) significantly potentiated the uptake of Aβ [11], situating SRs as the principal receptors responsible for senile plaques clearance.

Although the mechanistic factor involved in the association between AD and aging is still an unsolved question, there is evidence pointing out to microglial aging as well as other age-related changes as responsible for this correlation [9]. Studies of adult cortical cells have shown a reduced capacity of aged microglia to phagocytose Aβ [29]. This decrease in phagocytic activity was mainly favored by a proinflammatory state [30]. In addition, it has been shown that Aβ has cytotoxic effects only in aged individuals, with no Aβ-induced neurodegeneration observed in the brain of young animals [31].

All these microglial-mediated effects observed in AD are contrasted to the normally neuroprotective role of microglia, which involves the phagocytic capacity responsible for brain surveillance from infection and physical injuries, the supportive role implicated in neuronal survival by secreting nerve growth factors, and the contribution in creating a microenvironment for central nervous system (CNS) regeneration [32, 33]. These changes in normal microglial cell functions are usually explained as a switch in the inflammatory state of the cell: during aging (and possibly also in AD), microglia change from an M2 activation state, characterized as an anti-inflammatory phenotype associated with wound healing, to an M1 state, which is a proinflammatory activation state related to the production of inflammatory cytokines, chemokines, and reactive intermediates [34].

This evidence leads us to propose that aging, which is commonly associated with a progressive inflammatory state of the brain, can be one of the most important causes of the defective clearance of neurotoxic Aβ, which in turn favors the overstimulation of the immune response, creating a positive feedback that leads to neuronal dysfunction, neurodegeneration, and the progressive development of neurodegenerative diseases like AD.

3.2. Astrocytes Response

As for microglia, astrocytes have also been observed in close proximity to senile plaques of AD patient brains [35]. Moreover, Aβ is capable of stimulating the production of MCP-1 in astrocytes [36], having an important role in chemotaxis for attracting immune cells to the senile plaque.

In AD patient brains, an upregulation of IFN-γ receptor (IFNGR) on activated astrocytes has been observed, where treatment with INF-γ resulted in reduced cell viability [37], suggesting that activated astrocytes can become neurotoxic at least under certain conditions of inflammatory stimulation.

Under physiological conditions, astrocytes are the cells that maintain the brain integrity: they provide metabolic support for neurons; are capable of sensing and modulate the neuronal environment; regulate the synaptic levels of glutamate, ion concentrations, and the acid-base balance; synthesize and release antioxidant molecules; participate in the formation of the blood brain barrier; and function as immune competent cells by acting in the clearance of cell debris and as antigen presenting cells [38]. However, the effects mediated by astrocytes in AD are mainly harmful [39], which reveals the dual properties of astrocytes depending on the cellular context in which they are immersed.

In AD animal models, it has been demonstrated that astrocytes surrounding Aβ plaques are immunopositive for IL-6 [40]. In the same line of evidence, in vitro experiments show that Aβ exposure has differential immune effects in astrocytes depending on the peptide conformation: oligomeric Aβ induce transient high levels of IL-1β with a fast decrease, increasing nitric oxide (NO) production, inducible nitric oxide synthase (iNOS) and TNF-α expression, consistent with an early inflammatory response, while fibrillar Aβ induces persistent increased levels of IL-1β that remains over time, corresponding to a more chronic response [41]. The release of IL-1β by Aβ-stimulated astrocytes promotes the release of IL-1β, IL-6, and TNF-α by microvascular endothelial cells, suggesting that astrocytes-cytokine release also plays a role in neuroinflammation and endothelial response that contribute to AD progression [42].

In vitro studies have also shown that astrocytes exposed to Aβ present sporadic cytoplasmic calcium signals that correlate with the death of adjacent neurons, an effect that is, abolished by pretreating cells with heavy-metal chelators [43]. This effect suggests a neurotoxic effect mediated by intracellular calcium increase in astrocytes induced by Aβ. In addition, it was found that astrocytes exposed to Aβ have an increased glucose uptake and hydrogen peroxide production with no changes in intracellular antioxidants, both effects mediated by activation of the PI3K pathway [44], indicating that Aβ induces alterations of astrocytes metabolism [45] that could result in increased cytotoxicity.

Using specific deletion of the immune calcineurin/nuclear factor of activated T-cell (NFAT) pathways in astrocytes, which mediates biochemical pathways leading to astrocytes activation, it has been shown in AD animal models that activated astrocytes are responsible for cognitive and synaptic function impairment mediated by amyloid depositions [46], confirming a deleterious role of activated astrocytes in AD.

Nevertheless, even though activated astrocytes appear to have a deleterious role in AD progression, there is also evidence showing that they are capable of ameliorating the cytotoxic effects of activated microglia in culture. Conditioned media from microglia exposed to Aβ induce apoptosis in hippocampal cells, but this effect is not observed when the media is obtained from mixed glial cultures exposed to Aβ. Many of the inflammatory activation changes of microglial cell induced by Aβ are attenuated in the presence of astrocytes [47]. Moreover, astrocytes activation mediated by LPS and IFN-γ induce the secretion of TGF-β, a neuroprotective cytokine, which was capable of reducing apoptosis of hippocampal cells induced by Aβ [48], suggesting that astrocytes have a pivotal role in the modulation of AD inflammation.

Although the mechanisms that mediate astrocytes changes induced by Aβ are poorly understood, there is evidence showing that astrocytes are capable of phagocytosing Aβ and that they interact with Aβ through the SRs [23], specifically pointing out to SR-A as responsible for this interaction [35, 44, 49], which allows one to infer that, as in microglia, the phagocytic activity by astrocytes could be impaired with aging. Furthermore, given the high number of astrocytes in the brain parenchyma, even if the phagocytic activity of astrocytes appears to be less robust than that of microglia, changes in phagocytosis can be highly relevant for a decreased Aβ clearance capability, as well as impairment of the regulation of microglial cells [9].

3.3. Scavenger Receptors in AD

Cells mediating the immune response interact with multiple environmental compounds, and depending on receptors present on their surface, their response to those signals could be pro- or anti-inflammatory. Many pattern recognition receptors (PRR) have been described, like Toll-like receptors (TLR) and Nod-like receptors (NLR) that trigger the activation of specific inflammatory pathways according to the ligand they bind [50]. In addition, many immune cells are able to phagocytose diverse compounds because of the presence of receptors that uptake various ligands such as cell debris and allow their removal through the lysosomal pathway [51]. Many of these receptors belong to the scavenger receptors (SRs) family, a term that was first coined in 1979 to define high-affinity binding sites for acetylated low-density lipoproteins (acLDL) on macrophages [52]. These receptors share the capability of binding polyanionic ligands without differentiating exogenous ligands like those from pathogens and endogenous ligands, which have importance in the host defense response.

Whereas participation of SRs has been widely described in atherosclerosis, their role in AD-associated immune response remains poorly understood. However, it has been shown that SRs have an important role in the clearance of Aβ, and that the expression of these receptors decreases in aging brains of animal models of AD [53], situating SRs as important mediators of AD progression.

Until now 6 families of SRs have been described, named from SR-A to SR-F, but there are still 3 SRs that remain unclassified, which are RAGE, CD136, and SR-PSOX. It is unknown if the last two receptors are associated with the pathophysiology of AD, even though both are expressed in the CNS [54]. In this section we will discuss the main SRs that appear to be involved in AD and their role in glial cell inflammatory activation (Figure 1).

Figure 1

Summary of the main characteristics and functions played by SRs in inflammation and AD. The left panel shows changes induced by the inflammatory activation of SRs reviewed in the text. The right panel resumes the principal alterations induced by the activation of SRs mediated by the amyloid peptide.

3.4. SR-BI

The principal ligand of SR-BI is HDL [55], which has an important role in lipid and cholesterol mobilization in the “reverse cholesterol transport” [56]. Because of the delivery of cholesterol from peripheral tissue occurs in SR-BI-expressing cells participating in lipid metabolism, the main expression of this receptor can be found in the liver and in steroidogenic tissues. Nevertheless, SR-BI can be also found in the brain parenchyma, especially on glial cells [49] and cerebral arterial smooth muscle [57].

It is believed that SR-BI has a role in host defense [58] because of the upregulation of its expression during phagocytic and dendritic differentiation of monocytes and because of the suppression of its expression in monocytes and macrophages, exposed to proinflammatory stimuli [59]. Moreover, SR-BI-null mice have a 100% fatality induced by sepsis with increased levels of inflammatory cytokines released by macrophages [60], while overexpression of SR-BI attenuated the inflammatory response in these cells [61], suggesting a protective role of SR-BI through the modulation of the inflammatory response of macrophages.

In astrocytes, the main role of SR-BI appears to be associated with clearance of apoptotic cells [62]. However, it has also been reported that SR-BI is involved in the adhesion of microglia to Aβ plaques [63]. Studies have shown that animal models for Aβ accumulation have an increased expression of SR-BI in the brain, and partial or total deletion of SR-BI gene in those animals enhances Aβ deposition associated with an impaired response of perivascular macrophages to Aβ [64]. However, if SR-BI has a direct role in Aβ clearance and if the interaction between Aβ and SR-BI activates specific signaling pathways remain as unanswered questions.

3.5. CD36

CD36, another member of the SR-B family, was initially described in adipocytes and myocardium, where it participates in the transport of long-chain fatty acids (LCFA) [65]. The deficiency of CD36 leads to an increase in plasma levels of free fatty acids and triacylglycerol, with an abnormal myocardial LCFA uptake [66]. CD36 is also expressed in immune cells, being associated with the clearance of apoptotic neutrophils by macrophages [67]. In the brain, the expression of CD36 has been reported in capillary endothelium [68], astrocytes [69], and microglial cells [70], in which this receptor has been associated with the regulation of cell migration [71].

CD36 appears to be involved in pathologies such as brain ischemia, where CD36 expression is increased mostly in cells expressing the microglia/macrophage marker CD11b. CD36-null mice have reduced infarct size after ischemia, improved neurological function, and, less ischemia-induced reactive oxygen species (ROS) levels than wild-type animals [72]. CD36-null mice also have an attenuated postischemic activation of NFκB, suppressed glial activation [73], and an impaired astrocytes proliferation [69], all of which situate CD36 as an important mediator for brain inflammatory events.

Besides brain ischemia, Coraci et al. detected reduced levels of CD36 in microglia obtained from patients with AD, multiple sclerosis, and Parkinson's disease [70]. Specifically, in AD, CD36 appears to have a major role in the binding of cells of the monocyte/macrophage lineage to Aβ, which activates a signaling pathway associated with production of ROS and cytokines [74, 75]. In CD36-null mice, microglia and macrophages have reduced secretion of cytokines, chemokines, and ROS in response to treatment with Aβ, in addition to showing a decreased macrophage and microglial recruitment into the brain [76].

In contrast to the reports by Coraci et al. [70], Ricciarelli et al. reported high expression of CD36 in the cerebral cortex of AD patients and in normal subjects with diffuse amyloid plaques, compared with the amyloid-free brains of control individuals. Also, by using cells in vitro, they demonstrated that Aβ-induced CD36 overexpression in neurons was associated with an increase in nitrated proteins [77]. Nonetheless, CD36 expression by leukocytes is significantly reduced in AD patients, a phenomenon already observed at early preclinical stages as mild cognitive impairment [78].

Otherwise, in animal models of AD, it has been shown that old mice had a decreased expression of CD36 associated with an increased secretion of IL-1β and TNF-α [53], and an increased vascular amyloid deposition mediated by CD36 [79].

The ability of CD36 to participate in the clearance of Aβ has been demonstrated by Shimizu et al., who by using CHO cells overexpressing CD36, showed a dose-dependent degradation of labeled Aβ, during treatment with an anti-CD36 antibody blocked Aβ degradation [80]. In addition, astrocytes-mediated Aβ clearance is also attenuated with neutralizing antibodies against CD36 [81].

Although there are only few studies that associate CD36 with Aβ clearance, it appears that this receptor is mostly associated with neurovascular dysfunction observed in AD. In animal models of AD, deficiency of CD36 prevents cerebrovascular effects and oxidative stress elicited by Aβ [79, 82], suggesting that CD36 could be a therapeutical target mainly for the treatment of neurovascular dysfunction in AD patients.

3.6. RAGE

RAGE is a member of the immunoglobulin family and a cell surface receptor for advanced glycation endproducts (AGEs), which accumulate mainly in vascular tissues in aged individuals [83]. RAGE protein expression can be found in vasculature, endothelium, smooth muscle, mononuclear cells, cardiac myocytes, and neural tissue [84].

The interaction of RAGE with the ligand amphoterin, a polypeptide associated with the growth of cortical neurons derived from the developing brain, has been linked to cancer as the colocalization of both molecules has been shown to contribute to cellular migration and tumor invasion. Blockade of this interaction leads to suppression of the activation of intracellular pathways linked to tumor proliferation [85].

Interaction of AGEs with RAGE expressed by endothelial cells has been usually related to vascular dysfunction, mainly because of ROS induced by AGEs. This oxidative stress results in the activation of NFκB pathway [86], an affect that has been also observed in inflamed gut biopsies with a significant upregulation of RAGE [87], situating RAGE as an important inflammatory mediator in AGEs mediated lesions.

In relation to AD, the interaction of Aβ with RAGE expressed by endothelial cells of the brain favors the transendothelial migration of monocytes from peripheral blood into the brain, indicating an important role of RAGE in AD-related vascular disorders [88]. Also, an increased expression of RAGE by neurons in the brain of AD patients has been observed. Murine models of AD with overexpression of RAGE have an exacerbated impairment in spatial learning/memory and altered activation of synaptic plasticity markers [89], where the synaptic depression and LTD impairment induced by Aβ could be rescued by functional suppression of RAGE activity in microglia [90]. However, Vodopivec et al. have shown that the absence of RAGE in animal models of AD does not ameliorate their cognitive deterioration, Aβ accumulation, or microglial activation [91], suggesting that RAGE would have only a secondary role for the impairments observed in AD.

3.7. SR-A

Scavenger receptor class A (SR-A) is a homotrimeric transmembrane glycoprotein containing extracellular C-terminal cysteine-rich domains, that was initially implicated in the development of atherosclerosis, because of its colocalization with macrophages of lipid-rich atherosclerotic lesions [92, 93]. The expression of this receptor has been detected in many tissues, including liver, placenta and brain [94]. When discovered, the first function described for SR-A was to provide adhesiveness to monocytes and macrophages to glycated collagen-IV-coated surfaces, and to mediate the endocytosis of acLDL [95]. Also, given the fact that macrophage SRs are involved in the binding and internalization of LPS, which is part of Gram-negative bacteria [96], Thomas et al. showed that SR-A-deficient mice were more susceptible to infection with pathogens, with an impaired ability to clear bacterial infection, confirming what was shown by Suzuki et al., providing the first insight on the importance of SR-A in host defense [97, 98]. Additionally, other researchers observed that these animals showed a reduced expression of IL-1β, which is associated with a reduced mortality in response to LPS [99], showing that SR-A has a role in the macrophage activation induced by endotoxin shock [100-104].

In addition, SR-A also plays a role in macrophage engulfment of apoptotic thymocytes [105, 106], and in atherosclerosis, observing that disruption of the SR-A gene results in a reduction in the size of atherosclerotic lesions [98]. Moreover, in left ventricular remodeling after myocardial infarction, SR-A has a role in attenuating cardiac remodeling by suppressing macrophage polarization toward a biased M1 phenotype, reducing the release of proinflammatory cytokines [107].

It is important that in contrast to most SRs, SR-A expression is not downregulated by chronic exposure to endogen ligands such as acLDL. On the opposite, SR-A expression can be reversibly increased by incubating macrophages with SR-A ligands [108]. In addition, binding of a ligand to SR-A activates PI3K recruits more receptors to the membrane surface [109], all of which are key functional characteristic to consider when SR-A is seen as a therapeutic target.

In the normal brain, SR-A is expressed by microglia, perivascular cells, microvessels, stromal, epiplexus, and meningeal macrophages [110-114]. Furthermore, our group was the first to describe the expression of SR-A by astrocytes, showing that exposure to SR-A ligands activated MAPKs and NFκB signaling pathways and increased the production of IL-1β and NO by astrocytes [115].

In an animal model of cerebral ischemic injury, SR-A is upregulated in the brain, an effect that correlates with increased levels of proinflammatory markers in microglia/macrophages, and an increased activation of NFκB; whereas SR-A-deficient mice show a reduced infarct size and improved neuronal function, suggesting the participation of SR-A into the M1 microglia/macrophage polarization [116-118].

In AD, SR-A has been observed in close association with senile plaques [111], presenting microglia positive for the receptor [114, 119]. SR-A has been related to rodent microglia and monocyte adhesion to Aβ coated surfaces, leading to the production of ROS [120] and to Aβ internalization mediated by endosomes in microglia [57, 121, 122]. More specifically, Aβ internalized through SR-A is trafficked toward lysosomes inside the microglia and degraded by cathepsin B [123]. To our knowledge, SR-A appears to be the most important scavenger receptor of the brain participating in Aβ clearance. For this reason, SR-A could be a potential therapeutical target in the treatment of AD.

3.8. SR MARCO

The macrophage receptor with collagenous structure (MARCO) is a member of the SRs class A family, localized mainly in macrophages of the spleen and lymph nodes [124], acting in the binding of bacterial antigens and phagocytosis, and having an important role in host defense [125]. In the presence of pro-inflammatory stimuli like LPS, SR MARCO expression is upregulated even in macrophages from liver and lungs, where normally it is not expressed [126]. It is believed that SR MARCO has a direct effect in the morphology of activated macrophages, which is necessary for trapping pathogens, by mediating the formation of lamellipodia-like structures and dendritic processes [127]. In fact, SR MARCO expression is essential for dendritic cells to acquire a mature phenotype [128].

In the CNS, SR MARCO is present in microglia and astrocytes; SR MARCO expression in microglia is associated with a decrease of the antigen internalization capacity [128], while for both astrocytes and microglial cells it is believed that SR MARCO participates in their adhesion to Aβ [49].

3.9. Other SRs in AD

There are other SRs that have been involved in the signaling mediated by Aβ, which we will briefly mention because of the scarce evidence that relates them directly to the pathophysiology of AD.

3.9.1. CD68

This receptor, also known as macrosialin, is a member of the lysosomal-associated membrane protein (LAMP) family, which is expressed in macrophages, osteoclasts, dendritic cells, and microglia, where its principal role is to bind and uptake oxidized lipoproteins and apoptotic cells [129]. Although there are no studies involving CD68 in AD, Argiles et al. showed that patients with haemodialysis-associated amyloidosis show an upregulated expression of CD68 by macrophages [130].

3.9.2. OLR1

The oxidized LDL receptor 1 (OLR1) binds LDL, being an important SR associated with atherosclerosis, is mainly expressed by endothelial cells and monocytes, with minor expression by macrophages [131]. Even though it is unknown if OLR1 is expressed by microglia, and if the receptor has a direct role in the immune response, it has been shown that OLR1 is associated with Aβ transport across the blood brain barrier [132, 133].

3.9.3. MEGF10

Multiple EGF-like domains 10 (MEGF10) is a type 1 transmembrane protein containing 17 EGF-like domains in the extracellular portion [134] and is mainly expressed in the brain, and it has been shown to be implicated in the uptake of Aβ mediated by the lipid rafts endocytosis pathway [135]. Nevertheless, MEGF10 expression has not been observed in glial cells; therefore, the mechanism by which this receptor could participate in Aβ clearance is unknown.

4. Conclusion

When AD is visualized as a pathology caused by a dysfunction of glial cells, which compromise several of their protective functions, including the phagocytosis of Aβ, and favors potentially deleterious effects, as those observed in dysregulation of the inflammatory regulation, an objective target to generate potential treatments should be the recovery of the protective activation of glia, characteristics that appear to be lost in association with aging and chronic inflammatory activation. Most of SRs found in glia appear to be potentially involved in phagocytosis and inflammatory activation of glial cells. However, they have been poorly studied in terms of their interaction with the Aβ peptide.

As it was shown by Hickman et al., the age progression associated with AD reduces the expression of SR-A in older individuals, an effect that is, also induced by treating microglial cells with pro-inflammatory cytokines [53]. This robust evidence situates SR-A as one of the main receptors involved in the impaired clearance of Aβ observed in AD and also could be the link between AD and the inflammatory state related to aging, suggesting that SR-A could be an interesting therapeutic target for AD.