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PLoS One. 2012; 7(9): e45069.
Published online Sep 12, 2012. doi:  10.1371/journal.pone.0045069
PMCID: PMC3440417

Astrocyte Senescence as a Component of Alzheimer’s Disease

Jialin Charles Zheng, Editor

Abstract

Aging is the main risk factor for Alzheimer’s disease (AD); however, the aspects of the aging process that predispose the brain to the development of AD are largely unknown. Astrocytes perform a myriad of functions in the central nervous system to maintain homeostasis and support neuronal function. In vitro, human astrocytes are highly sensitive to oxidative stress and trigger a senescence program when faced with multiple types of stress. In order to determine whether senescent astrocytes appear in vivo, brain tissue from aged individuals and patients with AD was examined for the presence of senescent astrocytes using p16INK4a and matrix metalloproteinase-1 (MMP-1) expression as markers of senescence. Compared with fetal tissue samples (n = 4), a significant increase in p16INK4a-positive astrocytes was observed in subjects aged 35 to 50 years (n = 6; P = 0.02) and 78 to 90 years (n = 11; P<10−6). In addition, the frontal cortex of AD patients (n = 15) harbored a significantly greater burden of p16INK4a-positive astrocytes compared with non-AD adult control subjects of similar ages (n = 25; P = 0.02) and fetal controls (n = 4; P<10−7). Consistent with the senescent nature of the p16INK4a-positive astrocytes, increased metalloproteinase MMP-1 correlated with p16INK4a. In vitro, beta-amyloid 1–42 (Aβ1–42) triggered senescence, driving the expression of p16INK4a and senescence-associated beta-galactosidase. In addition, we found that senescent astrocytes produce a number of inflammatory cytokines including interleukin-6 (IL-6), which seems to be regulated by p38MAPK. We propose that an accumulation of p16INK4a-positive senescent astrocytes may link increased age and increased risk for sporadic AD.

Introduction

Alzheimer’s disease (AD) is the most common cause of dementia, accounting for 60–80% of all cases [1]. The disease is characterized by brain atrophy, extracellular deposition of beta-amyloid (Aβ) peptide, intra-neuronal accumulation of phosphorylated tau, neuronal and synaptic loss, and inflammation. Despite being the focus of intense research, the cause of AD, especially sporadic AD, is still unclear. The greatest risk factor for AD is aging, although the mechanism underlying the contribution of aging to the development AD is poorly understood.

A recent development in the basic biology of aging, with possible implications for AD, is the recognition that senescent cells accumulate in vivo [2][4]. Although senescent cells increase with age in several tissues [5], little is known about the potential appearance of senescent cells in the brain. The senescence process is an irreversible growth arrest that can be triggered by various events including telomere dysfunction, DNA damage, oxidative stress, and oncogene activation [6]. Although it was once thought that senescent cells simply lack function, it is now known that senescent cells are functionally altered. They secrete cytokines and proteases that profoundly affect neighboring cells, and may contribute to age-related declines in organ function [7]. For example, senescent fibroblasts produce an altered secretory pattern referred to as the senescence-associated secretory phenotype (SASP) [8]. The SASP is characterized by the expression of a complex mixture of factors including reactive cytokines and proteases that create a proinflammatory microenvironment. The relevance of senescent cells to the aging process has been demonstrated by the phenotypic improvement observed following the targeted removal of senescent cells in a progeroid mouse model [9].

Astrocytes comprise a highly abundant population of glial cells, the function of which is critical for the support of neuronal homeostasis. Astrocytes regulate the contents of the synaptic cleft and synaptic transmission as part of the tripartite synapse, control CNS metabolism, and maintain blood brain barrier integrity [10], [11]. Impairment of these functions through any disturbance in astrocyte integrity is likely to impact multiple aspects of brain physiology. Interestingly, astrocytes undergo a functional decline with age in vivo that parallels functional declines in vitro [12]. We demonstrated that in response to oxidative stress and exhaustive replication, human astrocytes activate a senescence program accompanied by the expression of p16, p21, p53, 53BP1; G1 cell cycle arrest; a reduction in telomere length; and increased co-localization of the histone chaperone HIRA and the promyelocytic leukemia PML proteins, a requirement for the formation of senescence-associated heterochromatin foci [13].

The importance of senescent astrocytes in age-related dementia has been the subject of recent discussion [14], but to date, there is little evidence to suggest that senescent astrocytes accumulate in the brain. In this study, we examined brain tissue from aged individuals and patients with AD to determine whether senescent astrocytes are present in these individuals. Our results demonstrate that senescent astrocytes accumulate in aged brain, and further, in brain from patients with AD. Furthermore, since Aβ peptides induce mitochondrial dysfunction, oxidative stress, and alterations in the metabolic phenotype of astrocytes [15][17]; we examined whether Aβ peptides initiate the senescence response in these cells. In vitro, we found that exposure of astrocytes to Aβ1–42 triggers senescence and that senescent astrocytes produce high quantities of interleukin-6 (IL-6), a cytokine known to be increased in the CNS of AD patients [18]. Based on this evidence, we propose that accumulation of senescent astrocytes may be one age-related risk factor for sporadic AD.

Results

1-42 Peptide Leads to Astrocyte Senescence

The mechanisms of Aβ-induced neurotoxicity are not fully understood; however, recent studies suggest a role for nonfibrillar soluble oligomers of Aβ in the deleterious effects of Aβ on synaptic plasticity and learned behavior [19][22]. Human astrocytes are highly susceptible to stress and undergo a senescent arrest following cellular damage [13], and in order to determine whether a role exists for soluble Aβ1–42 in the initiation of senescence in human astrocytes in vitro, we treated cells with either conditioned media from Aβ-secreting CHO cells or with synthetic oligomerized Aβ1–42 peptide and evaluated markers of cellular senescence. Treatment with either Aβ conditioned media or Aβ1–42 peptide induced senescence-associated beta-galactosidase (SA β-gal) activity (Figures 1A, 1B) and increased expression of the p16INK4a senescence biomarker (Figure 1C).

Figure 1
Astrocytes trigger senescence in response to Aβ1–42.

Senescent Astrocytes Display Characteristics of Senescence-associated Secretory Phenotype (SASP) in vitro

Due to the potential impact of senescent cells on tissue microenvironment, it is important to characterize the secretory pattern that is produced during senescence. We examined the secretory pattern of senescent astrocytes using a protein expression array. This analysis revealed an elevated production of multiple inflammatory cytokines by senescent astrocytes. The most dramatic increase was observed in IL-6 production, which increased 10-fold. Production of RANTES, IL-8, and ICAM-1 was elevated at least 2-fold relative to pre-senescent astrocytes (Figure 2). Increased cytokine production was specific to a subset of cytokines; for example, IL-2, IL-3, and IL-4 showed little to no induction relative to IL-6. One component of the SASP present in multiple cell types is IL-6. IL-6 may act in concert with other pro-inflammatory cytokines to induce local inflammatory responses including the recruitment of natural killer cells to aid in the clearance of senescent cells [14]. In addition to its association with fibroblast senescence [8], [23], IL-6 is thought to be a major mediator of chronic inflammation associated with aging and aging-related diseases including AD [24][26].

Figure 2
Senescent astrocytes secrete pro-inflammatory mediators that may constitute a SASP.

The population of senescent astrocytes increases in human brain during aging and AD

Having established that Aβ can induce senescence in vitro, we examined brain tissue from patients of differing ages and those with AD (See Table S1 for patient demographics and clinical history) for p16INK4a expression. p16INK4a has emerged as a robust in vivo biomarker of senescence in human and rodent tissues [27], [28]. Frontal cortices of 44 cases (4 fetal and 40 adult) were screened for p16INK4a-positive astrocytes using double immunofluorescence for p16INK4a and the astrocyte marker GFAP (Figure 3A). Although the average age at initial presentation of AD ranges from 68–73 years across different ethnicities, neuropathologic changes characteristic of AD can precede clinical symptoms by up to twenty years [29], [30]. We selected the age ranges of 35–50 years and 78–90 years (Figure 3B) in order to compare a group that is least likely to have AD and a group that is most likely to have AD [31]. Normal adults exhibited a 6- to 8-fold increase in the number of astrocytes expressing p16INK4a compared with fetal cortices, suggesting an accumulation of p16INK4a-positive astrocytes with aging (Figure 3B). This is consistent with reports indicating similar in vivo increases in p16INK4a in human aged skin [27], kidney [32], lung [33], and heart [34]. Frontal cortices from AD patients demonstrated a significant increase in p16INK4a expression when compared to age-matched controls (Figure 3C). Overall, there was an increase in p16INK4a-positive astrocytes from fetal to non-AD adults and from non-AD to AD adults. This suggests that senescent astrocytes do accumulate with normal aging, and increase further in the setting of AD. Cerebellar astrocytes (AD and similar-aged controls) failed to demonstrate an increase in p16INK4a expression (Figure 4). This finding is consistent with a diffuse cerebellar amyloid plaque formation and relative lack of cerebellar pathology in AD [35], [36].

Figure 3
Increased frequency of senescent astrocytes during brain aging and AD.
Figure 4
Expression level of p16INK4a is not elevated in adult cerebellar astrocytes.

Increased secretion of matrix metalloproteinase-1 (MMP-1) during senescence of human fibroblasts may affect the remodeling of the extracellular matrix and tissue function during aging [37]. Consistent with the senescent nature of the p16INK4a-positive astrocytes, increased MMP-1/collagenase correlated with p16INK4a during brain aging, suggesting that senescent astrocytes may have an altered pattern of secretion in vivo with potential consequences for the microenvironment (Figure 5A). As shown in Figure 5B, p16INK4a and MMP-1 staining in astrocytes demonstrated a positive correlation with each other (Spearman correlation coefficient 0.574, P = 0.02). Comparison of MMP-1 expression based on the presence or absence of comorbidities did not reveal any significant differences (data not shown).

Figure 5
MMP-1 expression parallels p16INK4a expression in human astrocytes in vivo.

p38MAPK is Activated in Senescent Astrocytes and is Required for Generation of the SASP

Whereas p16INK4a is a robust biomarker for detecting senescent astrocytes both in vitro and in tissues, elevated expression of this cyclin-dependent kinase inhibitor is not essential for the generation of a SASP [38]. Therefore, we examined senescent astrocytes for activation of p38 mitogen-activated protein kinase (p38MAPK), which is a mediator of the senescence arrest in response to diverse stimuli [39] and a known regulator of the SASP in other cell types [40]. An increase in p38MAPK signaling has also been linked to the cognitive decline associated with AD pathophysiology [41], [42]. Activity of this stress-related kinase (assessed by phosphorylation of p38MAPK and heat shock protein 27 [Hsp27], a major downstream target of p38MAPK activation) increased dramatically during senescence in astrocytes (Figure 6A). In addition, pharmacological inhibition of p38MAPK abolished IL-6 secretion by senescent astrocytes (Figure 6B).

Figure 6
p38MAPK pathway is activated and modulates IL-6 secretion in astrocytes.

Discussion

Elevated markers of DNA damage have been observed in astrocytes found in regions of the brain that are vulnerable to AD [43]. While a role for senescent astrocytes in the aging brain has been postulated [14], evidence for the existence of these cells has been lacking. Our study provides evidence supporting the existence of senescent cells in the human brain. We demonstrated relatively high numbers of senescent astrocytes in brain tissue from aged individuals and patients suffering from AD. Further studies will be required in order to definitively demonstrate a casual connection between the appearance of senescent astrocytes and CNS dysfunction. Furthermore, the number of cases was limited by the availability of post-mortem samples. This was partly due to the low rate of autopsies in general [44].

Evidence coming mainly from fibroblast models indicates that senescent cells secrete pro-inflammatory mediators and proteases that not only potentiate clearance of senescent cells through immune surveillance, but may also contribute to age-related declines in organ function [7], [8], [45]. Consistent with these observations, we found that the accumulation of p16INK4a-positive astrocytes is accompanied by an increase in MMP-1/collagenase, a metalloproteinase able to degrade collagen types I, II, and III, at the extracellular matrix. In agreement with these results, increased expression of MMP-1 has been reported in normal senescent human and Werner fibroblasts [37], [46], [47]. Additionally, our in vitro data indicate an altered pattern of secretion in senescent astrocytes that is characterized by significant increases in IL-6 production. We propose a key role for p38MAPK in the regulation of IL-6 in these cells. Overall, these results provide support for a SASP in human astrocytes during aging in vivo. Several inflammatory markers found to be robustly changed in other cell types were not as dramatically altered in senescent (replicative) astrocytes according to our array [25]. Potential reasons for this discrepancy are the nature of senescence induction in the astrocytes and cell-type specific differences. Furthermore, only a subset of factors indicative of the SASP was measured in the antibody array. Further analysis will be required to determine whether the full breadth of SASP factors is altered in the secretion pattern of senescent astrocytes.

The data suggest that several factors may contribute to the appearance of p16INK4a-positive cells. The presence of comorbidities such as diabetes, hypertension, or chronic obstructive pulmonary disease correlated with the burden of p16INK4a-positive astrocytes. Also within our cohort of patients, a subset of patients exists with documented history of severe hypoxic episodes or cerebral ischemia. These patients show high positive staining for p16INK4a. This effect was most pronounced in a 49-year-old male AD patient with a family history of AD and neuropathologic evidence of hypoxia. Interestingly, similar p16INK4a levels were observed in a non-AD patient with a clinical history of repeated hypotensive and hypoxic events due to cardiac failure. Although patient numbers are too small to perform a statistical evaluation of the relationship between clinical history and the appearance of senescent astrocytes, we propose that the number of p16INK4a-positive astrocytes is a reflection of the cumulative impact of multiple stressors resulting from ischemic events, focal areas of cellular damage secondary to ROS production, Aβ deposition, or other insults. The fact that senescence is a common response to multiple injuries or genetic abnormalities supports the concept that the accumulation of p16INK4a-positive senescent astrocytes may link aging as a risk factor for sporadic AD. Interestingly, senescence in the CNS may not be exclusively limited to astrocytes. We observed nuclei that were positive for p16INK4a, but not GFAP, in the frontal cortex (data not shown). Senescence in other cell types of the CNS, including neurons, has been postulated as important risk factor for AD [48].

In vitro, the exposure of astrocytes to oligomeric species of Aβ1–42 peptides or cell-derived Aβ induces astrocyte senescence as measured by several markers of the senescent arrest. Similarly, Aβ peptides accelerate the senescence of endothelial cells in vitro and in vivo in the zebrafish model [49]. The level of soluble Aβ oligomers in AD brain correlates better with disease severity as compared with the level insoluble fibrillar Aβ [50]; therefore, we chose to use Aβ oligomers at concentrations previously shown to affect astrocytes [51], [52]. Compared with cell-derived Aβ, a considerably higher concentration of synthetic Aβ1–42 peptide, micromolar and nanomolar respectively, was required to induce senescence in cultured human astrocytes. The increased dosage of synthetic versus cell-derived Aβ oligomers required to trigger senescence, correlates with reports on the effects of Aβ on rat hippocampal long-term potentiation [53].

Thus, it appears that the cellular stress induced by Aβ results in activation of the senescence program. In fact, astrocytes are very sensitive to stress, rapidly triggering the senescent phenotype in response to a mild oxidative stress [13].Consistent with this concept, we have demonstrated that astrocytes cultured at 7% oxygen have an extension in their replicative life span compared with those cultured at 20% oxygen (Figure S1). Based on these results, and our previously published findings indicating increased sensitivity of astrocytes to oxidative stress [13], we hypothesize that there is a functional relationship between Aβ and senescence, and that Aβ may induce oxidative stress to trigger the senescent program in astrocytes, thereby contributing to astrocyte dysfunction. The chronic, subtle loss of astrocyte ability to maintain homeostasis throughout the CNS is now thought to underlie AD pathogenesis [54].

A common pathological feature of many neurodegenerative disease states, including AD, is reactive astrogliosis, which is a well-characterized spectrum of changes that occurs in astrocytes in response to a variety of insults [55]. It remains to be determined how our finding of stress-induced senescence in astrocytes relates to reactive astrogliosis; however, we propose that these two phenotypes may be interrelated given that astrocytes are highly susceptible to stress-induced changes. Based on the results presented here, we propose that the presence of senescent astrocytes contributes to the pathogenesis of AD and may represent a link between the aging process and progression of the disease.

Materials and Methods

Ethics Statement

All tissue samples were de-identified and obtained after approval by the Institutional Review Board at Drexel University College of Medicine (Protocol Number: 18172), and Institutional Review Board at University of Pennsylvania (Protocol Number: 180600). The protocols were approved as an exempt study. An honest broker de-identifed each specimen and no protected health information was made available to the researcher. The specimens were assigned de-identified numbers which could not be traced back to the patients. There is no link between patient identifiers and the data, therefore consent for this protocol was waived.

Human Frontal Cortex Samples

Archived, formalin-fixed, paraffin-embedded (FFPE) human frontal cortex (n = 44) and cerebellum (n = 6) slides were obtained from the Drexel University College of Medicine Department of Pathology & Laboratory Medicine’s autopsy service and the University of Pennsylvania’s Center for Neurodegenerative Disease Research. Samples were obtained from normal subjects aged 36 weeks to 92 years at autopsy. The fetal samples ranged in estimated gestational age from 36 to 39 weeks. Additional samples from patients with a diagnosis of AD at autopsy were obtained ranging in age from 49 to 90 years. Control subjects were nonschizophrenic subjects without AD.

Cell Culture

Human astrocytes were cultured at 37°C, 5% CO2 in astrocyte medium supplemented with 2% fetal bovine serum, growth supplement, and penicillin/streptomycin all obtained from ScienCell Research Laboratories (Carlsbad, CA). Cells were seeded at a standard density of 1 × 104 cells/cm2 and cultured until they reached 70% to 80% confluence. At each passage, astrocytes were trypsinized, counted, and the cumulative population doubling level (CPDL) was calculated as we have previously described [13].

Preparation of Oligomeric Beta-amyloid

Synthetic Aβ1–42 (American Peptide; Sunnyvale, CA) was oligomerized as described [56], [57]. Briefly, lyophilized Aβ1–42 was solubilized in hexafluoroisopropanol HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) to obtain monomers. Aβ1–42/HFIP aliquots were dried in low-protein binding tubes using a speedvac and the resulting peptide film was stored at −80°C until use. To generate oligomeric Aβ, the peptide film was dissolved in DMSO to a concentration of 5 mM and sonicated. The suspension was diluted in astrocyte medium to achieve the desired final concentrations and incubated at 4°C overnight. The presence of soluble Aβ oligomers in astrocyte medium following oligomerization was verified by immunoblotting of approximately 0.1 µg of synthetic peptide loaded onto a 12% SDS-PAGE gel (Figure S2).

Preparation of Conditioned Media from 7PA2 and CHO Cells

The 7PA2 cell line (kindly provided by Dr. E.H. Koo; University of California, San Diego) stably expresses the mutant amyloid precursor protein (APP) gene as previously described [58], and secretes Aβ peptides at levels similar to those found in human brains affected by AD and normal cerebrospinal fluid (~1–2 nM) [59]. The Aβ produced by these cells is biologically relevant as judged by a significant disruption in working memory when delivered to rats [22], [60]. CHO cells, originally derived from Chinese hamster ovary [61], were available and carried in our laboratory. Aβ-secreting 7PA2 or untransfected control CHO cells were grown to near confluence and incubated in serum-free DMEM or MCDB105 media for 24 hours. Conditioned media was collected and cleared of cells by centrifugation at 200 x g for 10 min at 4°C. Media was then concentrated 15X using 3,000 MWCO centrifugal filters (Millipore; Cork, Ireland). Concentrated media was stored at −80°C prior to treatment. The presence of soluble Aβ oligomers in conditioned media was verified by immunoblot using anti-Aβ antibody (2C8) (Santa Cruz Biotechnology; Santa Cruz, CA). Levels of Aβ in 7PA2 conditioned media are shown in Figure S2.

Staining for Senescence-associated β-galactosidase

Senescence-associated beta-galactosidase (SA β-gal) staining was performed as previously described [62]. Briefly, following exposure to Aβ peptides or conditioned media, astrocytes were fixed in 2% formaldehyde/0.2% glutaraldehyde for 5 minutes and stained for SA β-gal activity overnight. The percent of positive (blue) cells were counted and expressed relative to the level of positive cells in vehicle-treated controls. At least 200 cells were counted.

Analysis of Inflammatory Factors Secreted by Astrocytes

Pre-senescent (early-passage) and senescent (late-passage) human astrocytes were incubated with serum-free MCDB105 media to generate conditioned media. After a 48-hour incubation period, media was collected and cells were trypsinized and counted to determine the cell number for normalization. Human inflammation antibody array (RayBiotech, Inc.; Norcross, GA) was used to detect secreted inflammatory factors present in the conditioned media according to the product manual. The intensity of the signal on the array membranes was quantified by densitometry, normalized to cell number, and analyzed using the RayBio® Analysis Tool.

Role of p38MAPK in IL-6 Secretion

Human astrocytes were triggered to undergo stress-induced premature senescence by H2O2 treatment (200 µM for 2 hours). Five days following senescence induction, astrocytes were treated with 10 µM of the p38MAPK pharmacological inhibitor SB-203580 (Enzo Life Sciences Inc.; Farmingdale, NY) or vehicle for 48 hours and then incubated in serum-free MCDB105 for conditioned media collection. Pre-senescent astrocytes were also treated with 10 µM SB-203580 or vehicle in the same manner prior to conditioned media collection. Conditioned media was collected from pre-senescent and senescent cells after a 24-hour incubation period in serum-free MCDB105. The level of IL-6 in conditioned media was quantified by IL-6 ELISA (R&D Systems, Inc.; Minneapolis, MN) and normalized to cell number.

Immunoblotting

Early-passage human astrocytes were treated for 24 hours with oligomerized Aβ1–42 at a final concentration of 5 µM in astrocyte media; 0.05% DMSO was used as control. After 24 hours, media was replaced. Cell lysate was collected 4 days post-treatment in RIPA buffer. Western blot analysis was performed under standard conditions using 25 µg of total cell proteins for anti-p16INK4a (Santa Cruz Biotechnology; Santa Cruz, CA) and anti-β-actin (Sigma Aldrich; St. Louis, MO) as a loading control. In order to detect activation of the p38MAPK signaling pathway, antibodies recognizing p38MAPK and phospho-p38MAPK (Thr180/Tyr182) were obtained from Santa Cruz Biotechnology (Santa Cruz, CA), along with antibodies against Hsp27 (R&D Systems; Minneapolis, MN) and phospho-Hsp27 (Ser82) (Cell Signaling Technology; Danvers, MA).

Immunofluorescence

Slides were de-paraffinized with xylene, 3×5 minutes. After washes in 90% EtOH, 80% EtOH, 70% EtOH, and de-ionized water (2×5 min each), antigen retrieval was performed by heat-steam for 20 minutes in 10 mM citrate buffer pH 6.0. Slides were blocked in 5% normal goat serum, 5% normal donkey serum, 0.1% BSA, 0.25% Triton X-100 for 1.5 hours, then incubated overnight in a humidified chamber with anti-GFAP (Millipore; Temecula, CA), anti-p16INK4a (Santa Cruz Biotechnology, Inc.; Santa Cruz, CA) and anti-MMP1 (Lifespan Biosciences; Seattle, WA) primary antibodies. Slides were washed 3×5 minutes in 0.1% BSA and 0.1% Triton X-100, then incubated for 1 hour in the dark at room temperature with the secondary antibodies anti-rabbit Alexa Fluor 488 and anti-mouse Alexa Fluor 555 (both Invitrogen; Carlsbad, CA). After 3×5 minute washes in 1X PBS with 0.1% BSA and 0.1% Triton X-100, slides were incubated with DAPI, and mounted with Vectashield Mounting Medium (Vector Laboratories, Inc.; Burlingame, CA). Cells were visualized using an Olympus BX61 fluorescence microscope coupled with a Hamamatsu ORCA-ER camera and using Slide Book 4 software version 4.0.1.44 (Intelligent Innovations, Inc.; Denver, CO). 200-cell counts were performed at 40X magnification for p16INK4a-GFAP and MMP1-GFAP.

Statistics

Unless otherwise specified, all experiments were done at least in triplicate. Data are expressed as mean ± SD.

Supporting Information

Table S1

Clinical history obtained from post-mortem reports. A total of 44 cases (4 fetal and 40 adults) were included in the study. Adult ages ranged from 35 to 92 years (mean 72.3±17.4; 10 males, 15 females) for controls and 49 to 90 years (mean 77.6±11.44; 8 males, 7 females) for patients with AD. The average postmortem interval was 13.31±9.44 hours (N = 36, range 3 to 43.5 hours). Fetal samples were obtained from fetuses that died in utero and therefore had uncertain postmortem intervals. Cortical sections were obtained from the frontal cortex in all the adult cases.

(DOCX)

Figure S1

Effect of oxygen tension on replicative lifespan. Astrocytes were grown at 5% CO2 and either 20% or 7% oxygen. At every passage, cells were counted and the cumulative population doubling was calculated as described [13].

(TIF)

Figure S2

Detection of oligomerized Aβ peptide. Top gel, synthetic amyloid-β peptide (Aβ1–42) was diluted in astrocyte media to obtain a final concentration of 1µM and oligomerized as described. Astrocyte media with dimethyl sulfoxide (DMSO) alone was used as a control. A volume of media containing approximately 0.094 µg of synthetic peptide was loaded onto 12% gel. Western blot depicts the presence of small molecular weight oligomers of Aβ in astrocyte media. Bottom gel, conditioned media from 7PA2 cells contains secreted Aβ. 7PA2 and control CHO cells were incubated with serum-free DMEM or MCDB105 media for 24 hours to generate conditioned media. Conditioned media was collected and concentrated as described. Western blot showing presence of Aβ in conditioned media from 7PA2 cells.

(TIF)

Acknowledgments

We thank Dr. Edward H. Koo (University of California, San Diego) for kindly proving us with the 7PA2 cell line, and Dr. Leslie Sell for editorial assistance.

Funding Statement

The study was supported by National Institutes of Health/National Institute on Aging grants AG022443 (CS) and AG022443-S1 (CT); the Resident Research Fellowship, Drexel University College of Medicine, awarded to RB; the Medical Student Summer Research Fellowship, Drexel University College of Medicine, awarded to MM; and the Aging Initiative Fellowship, Drexel University College of Medicine, awarded to AB. EPC was supported by funds from the Department of Pathology, Drexel University College of Medicine. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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