Antiretroviral (ARV) therapy (ART) has effectively suppressed the incidence of human immunodeficiency virus (HIV)-associated dementia in HIV-1 positive individuals. However, the prevalence of more subtle forms of neurocognitive dysfunction continues to escalate. Recently, endoplasmic reticulum (ER) stress has been linked to many neurological diseases; yet, its role in HIV/neuroAIDS remains largely unexplored. Furthermore, upregulation of astrocyte elevated gene-1 (AEG-1), a novel HIV-1 inducible gene, along with ER stress markers in a Huntington’s disease model, suggests a possible role in HIV-associated ER stress. The current study is focused on unfolded protein responses (UPRs) and AEG-1 regulation in primary human astrocytes exposed to HIV-associated neurocognitive disorders (HAND)-relevant stimuli (HIV-1 virions, inflammation and ARV drugs). Interleukin (IL)-1β and the nucleoside reverse transcriptase inhibitor abacavir upregulated expression of ER stress markers in human astrocytes, including binding immunoglobulin protein (BiP), C/EBP homologous protein (CHOP), and calnexin. In addition, IL-1β activated all three well-known UPR pathways: protein kinase RNA-like ER kinase (PERK); activating transcription factor 6 (ATF-6); and inositol-requiring enzyme 1α (IRE1α). AEG-1 upregulation correlated to ER stress and demonstrated astrocyte AEG-1 interaction with the calcium-binding chaperone, calnexin. IL-1β and abacavir enhanced intracellular calcium signaling in astrocytes in the absence of extracellular calcium, illustrating ER-associated calcium release. Alternatively, calcium evoked in response to HAND-relevant stimuli led to mitochondrial permeability transition pore (mPTP) opening in human astrocytes. Importantly, IL-1β- and abacavir-induced UPR and mPTP opening were inhibited by the intracellular calcium chelation, indicating the critical role of calcium signaling in HAND-relevant ER stress in astrocytes. In summary, our study highlights that ARV drugs and IL-1β induced UPR, AEG-1 expression, intracellular calcium, and mitochondrial depolarization in astrocytes. This study uncovers astrocyte ER stress as a novel therapeutic target in the management of HIV-1-associated neurotoxicity and possibly in the treatment of neuroAIDS.
Human immunodeficiency virus (HIV)-1 invades the central nervous system (CNS) during early stages of infection and often leads to neurological complications known as HIV-associated neurocognitive disorders (HAND).1 While the success of antiretroviral (ARV) therapy (ART) has markedly reduced the incidence of the most severe neurological manifestation, that is, HIV-associated dementia, the prevalence of cognitive dysfunctions in HIV-1-positive patients despite ART remains high.2 In addition to persistent low-grade viral replication and inflammation within the CNS, ARV drug toxicity also likely contributes to neurological dysfunction in HIV-1 patients.3,
Endoplasmic reticulum (ER) stress has been implicated in several neurological diseases, including ischemia, brain trauma, Alzheimer’s, and Parkinson’s disease.8,9 The ER regulates key cellular functions, including protein synthesis and folding, calcium storage, and lipid biosynthesis. Physiological and pathological stimuli, such as serum-starved conditions, high protein demand, viral infections, and inflammatory cytokines, can disrupt ER homeostasis resulting in an accumulation of misfolded proteins.10 To mitigate ER stress, cells activate the unfolded protein response (UPR), which is regulated by three major pathways, each with its own initiator: protein kinase RNA-like ER kinase (PERK); activating transcription factor 6 (ATF6); or inositol-requiring enzyme 1α (IRE1α). The UPR promotes cell survival by attenuating protein translation and by inducing chaperone expression, ER-associated degradation of proteins, endogenous antioxidant responses, and autophagy. However, prolonged UPR activation can lead to orchestrated cell death, that is, apoptosis.11
Recent studies showed amyloid beta protein accumulation in brains of HIV-1-infected individuals, indicating the potential involvement of protein misfolding and UPR activation in HIV-1 pathogenesis.12,13 While UPR markers, including binding immunoglobulin protein (BiP) and ATF6 were significantly elevated in the CNS of HIV-1-positive individuals,14 the regulation of ER stress response in HIV-1-induced neuropathogenesis is not well understood.
During HIV-1 infection, several astrocyte-associated mechanisms lead to neurotoxicity, including excitotoxicity, inflammation, and oxidative stress.15 These mechanisms have also been linked to ER stress in neurodegeneration.16,17 In addition, recent studies showed HIV-1 transactivator of transcription (Tat) and glycoprotein (gp)120 protein expression in astrocytes induced ER stress-mediated cytotoxicity, possibly contributing to HIV-associated neuropathogenesis.18,19 Taken together, astrocytes represent a significant therapeutic target for reestablishing CNS homeostasis.
Recently, the multifunctional oncogene, astrocyte elevated gene-1 (AEG-1), was shown to dysregulate glutamate clearance by excitatory amino acid transporter 2 downregulation and HIV-associated neuroinflammation via upregulation of nuclear factor-κB (NF-κB) pathway in astrocytes.20,21 AEG-1 was also elevated in a Huntington’s disease model along with UPR markers such as BiP, C/EBP homologous protein (CHOP), and regulator of ribosome synthesis 1.22 These studies suggest the involvement of AEG-1 in ER stress responses during neurological diseases, including HAND.
In the present study, we investigated the role of HAND-relevant stimuli, inflammation (interleukin (IL)-1β) and the nucleoside reverse transcriptase inhibitor (NRTI), abacavir, in the induction of ER stress in astrocytes. We demonstrated that HAND-relevant stimuli increased astrocyte cytosolic calcium, which in turn, triggered ER stress and mitochondrial depolarization. Further, we investigated specific mechanisms through which these events were interlinked thus contributing to neurodegeneration. These findings are significant as prolonged activation of UPR due to severe/chronic ER stress likely has a critical role in HIV-associated neurodegeneration.
HAND-relevant stimuli initiate ER stress in primary human astrocytes
To mimic a HIV-related disease environment, astrocytes were treated with IL-1β and HIV-1. As a common mediator of neuroinflammation, IL-1β is primarily released by HIV-1-infected and immune-activated microglia in the CNS.23 Astrocytes are highly responsive to IL-1β and possess an autocrine loop to perpetuate activation.24 Here, primary human astrocytes were incubated with IL-1β (20 ng/ml) and HIV-1 (p24, 20 ng/ml) alone or in combination for 8 h, and ER stress marker mRNA levels were analyzed by real-time PCR (RT2-PCR; Figures 1a–c). IL-1β alone and in combination with HIV-1 significantly upregulated three UPR proximal initiators PERK (***P<0.001; Figure 1a), IRE1α (***P<0.001; Figure 1b), and ATF6 mRNA levels (***P<0.001; Figure 1c). On the other hand, HIV-1 alone did not alter expression of these markers. In parallel, downstream ER stress markers BiP, CHOP, and calnexin were evaluated (Figures 1d–f). In astrocytes, IL-1β alone and in combination with HIV-1 significantly increased expression of BiP (***P<0.001; Figure 1d), CHOP (*P<0.05, **P<0.01; Figure 1e), and calnexin mRNA (**P<0.01, ***P<0.001; Figure 1f). However, HIV-1, by itself, did not alter mRNA levels of tested markers as compared to controls. IL-1β was thus identified as a key ER stress inducer in human astrocytes during HIV-associated inflammation.
NRTIs trigger ER stress and AEG-1 expression in astrocytes
Despite the benefits attained with ARV regimen, the ‘successful failure’ of ART is that it effectively inhibits viral replication while concurrently triggering adverse side effects and toxicities.25,26 However, ART-associated toxicity in the CNS, particularly in glial cells, remains largely unexplored. To investigate ARV drug-mediated ER stress, astrocytes were treated with a wide range of ARV drugs, including NRTIs (abacavir, lamivudine, and stavudine), non-nucleoside reverse transcriptase inhibitors (NNRTIs; nevirapine and delavirdine), and protease inhibitors (PIs; darunavir, lopinavir, ritonavir, and saquinavir) at therapeutic doses (Figure 2). These ARV drugs were used clinically and have CNS penetration effectiveness (CPE) scores ranging from 1 to 4, with higher scores reflecting greater likelihood of CNS penetration.27 ER stress marker mRNA levels were evaluated 8 h post-treatment by RT2-PCR. Levels of PERK (***P<0.001; Figure 2a), ATF6 (***P<0.001; Figure 2b), and BiP mRNA (**P<0.01; Figure 2c) were significantly increased with abacavir or lamivudine treatments. The NNRTI delavirdine increased mRNA levels by ~1.5-fold, which was not statistically significant for PERK, ATF6, and BiP (Figures 2a–c). NRTIs (abacavir and lamivudine), NNRTIs (nevirapine and delavirdine), and PIs (lopinavir and ritonavir) significantly elevated AEG-1 mRNA as compared to respective controls (*P<0.05, **P<0.01, and ***P<0.001; Figure 2d). However, stavudine, darunavir, and saquinavir did not increase AEG-1 expression. As AEG-1 mRNA levels were elevated by ARV drugs with greater CNS penetration (i.e., abacavir, CPE 3; nevirapine, CPE 4; delavirdine, CPE 3; and lopinavir, CPE 3), exploring the effects of ART on AEG-1-regulated neurological outcomes is therapeutically relevant. Taken together, of all the ARV drugs tested, only abacavir and lamivudine triggered both UPR markers and AEG-1 upregulation. Therefore, considering its high CPE and current clinical use, abacavir was used to further study how ARV drugs regulate astrocyte ER stress.
HAND-relevant stimuli activate UPR and promote selective protein translation
The three distinct UPR pathways, PERK, IRE1α, and ATF6, can activate transcription of ER stress response element (ERSE)-regulated genes, including BiP and CHOP. Therefore, we next focused on identifying which specific UPR mechanism(s) regulate ER stress in astrocytes during inflammation and abacavir exposure. Western blot analysis confirmed increased eIF2α phosphorylation following IL-1β or abacavir treatment (*P<0.05; Figure 3a), suggesting that general attenuation of protein translation in astrocytes occurred via PERK activation. PERK-mediated eIF2α phosphorylation supports translation of ATF4, an ERSE transcription factor, normally suppressed by an inhibitory open reading frame. When active, eIF2α is abundant, and selective translation of ER stress mitigating genes is promoted.28 Our studies confirmed IL-1β significantly increased ATF4 levels in astrocytes (***P<0.001; Figure 3b). Next, to evaluate IRE1α- and ATF6-mediated UPR activation, whole-cell lysates were immunoblotted for the spliced form of XBP-1 (XBP-1s) and cleaved ATF6 (Figures 3c and d), the respective UPR-associated ERSE transcription factors. IL-1β significantly increased XBP-1s (***P<0.001; Figure 3c) and ATF6 (***P<0.001; Figure 3d) as compared to controls. Together, these results indicate that HAND-relevant stimuli induce transcriptional regulation during ER stress in astrocytes via each of the three UPR pathways: PERK, IRE1α, and ATF6.
IL-1β and abacavir transiently induce intracellular calcium in GCaMP6-transfected astrocytes
To investigate IL-1β- and abacavir-induced intracellular calcium ([Ca+2]i) signaling, primary human astrocytes were first transfected with GCaMP6 slow (GCamp6s) plasmid, a genetically encoded calcium sensor,29 with an ~80% transfection efficiency. Intracellular calcium was visualized by live, fluorescent, confocal imaging of GCaMP6s-transfected astrocytes. Baseline fluorescence was observed at 0 s (Figures 4a and d), which increased at 20 s after IL-1β and abacavir treatment (Figures 4b and e). Over time, fluorescence decreased returning to baseline by ~100 s (Figures 4c and f). Changes in fluorescence were reflective of calcium transients (ΔF=(F−F0)/(Fmax−F0), where F is the fluorescence intensity at any given time, Fmax is the maximum fluorescence intensity, and F0 is the baseline fluorescence intensity). Calcium changes induced with IL-1β, abacavir, and thapsigargin (Th), a known ER stressor, were plotted from representative astrocytes over time (Figure 4g). The dynamic changes in calcium transients were quantified using area under the curve to assess total change in calcium levels in a given astrocyte and to compare responses across treatments. IL-1β, abacavir, and Th each elicited significantly higher average [Ca+2]i than control (***P<0.001; Figure 4h, n=40 individual cells/treatment). Thus, these data validate that IL-1β and abacavir triggered transient intracellular calcium increase in astrocytes, comparable to that induced by Th.
HAND-relevant stimuli increase ER quality control mechanism in astrocytes
During ER stress, UPR activation increases chaperones such as BiP, calnexin, and calreticulin to promote proper protein folding and quality control in the ER.30 HAND-relevant stimuli increased calnexin levels in astrocytes (Figure 5). Astrocytes were treated with HIV-1 (Figure 5b), abacavir (Figure 5c), IL-1β (Figure 5d), HIV-1+IL-1β (Figure 5e), and abacavir+IL-1β (Figure 5f) for 24 h. Cells were fixed and immunostained for glial fibrillary acidic protein (GFAP; red), calnexin (green), and DAPI (blue). Untreated astrocytes retained bright GFAP with lower perinuclear calnexin staining (Figure 5a). HAND-relevant stimuli (Figures 5b–f) increased calnexin expression in astrocytes.
AEG-1 colocalizes and interacts with calnexin in the context of ER stress
As a pleotropic protein, AEG-1 can localize to the cell membrane, cytoplasm, ER, nucleus, and nucleolus, and exhibits diverse location-related functions.31 AEG-1 colocalized with calnexin in the ER, which was increased with IL-1β+tumor necrosis factor (TNF)-α, and Th treatment (Figures 5g–i) when assessed by confocal microscopy. To study how ER stress influences AEG-1, astrocytes were treated with ER stress inducing agents brefeldin A (Bf), tunicamycin (Tm), and Th followed by RT2-PCR analysis (Figure 5j). These ER stressors significantly upregulated AEG-1 mRNA levels as compared to controls (**P<0.01, ***P<0.001; Figure 5j). Both Tm and Th upregulated AEG-1 by 2.5-fold (Figure 5j), a feature that is rather uncommon for AEG-1, which primarily exhibits its function via subcellular localization and redistribution.31 Moreover, AEG-1 transcripts correlated significantly to BiP (R2: 0.49, ***P<0.001; Figure 5k) and PERK (R2: 0.92; ***P<0.001; Figure 5k) in the ARV drug-exposed astrocytes (shown earlier in Figure 2). AEG-1 is also known to exhibit diverse functions by interacting with several cellular proteins in cancer.32 As AEG-1 can function as a transcriptional coactivator and as a scaffolding protein, we examined whether AEG-1 directly binds to calnexin (Figure 5l). Consistent with the confocal analyses, coimmunoprecipitation data confirmed AEG-1 interacted with calnexin in untreated, IL-1β-, abacavir-, or Th-treated astrocytes (Figure 5l). These results establish that AEG-1 expression is elevated during HAND-associated ER stress. Furthermore, a direct interaction with the calcium-binding chaperone calnexin indicates that AEG-1 likely regulates ER quality control and possibly calcium signaling in astrocytes.
HAND-relevant stimuli lead to mitochondrial permeability transition pore opening in astrocytes
Cross talk between neurodegenerative mechanisms, including inflammation, oxidative, and ER stress, increases the severity of many diseases.17 A persistent increase in [Ca2+]i in response to pathophysiological stimuli can lead to mitochondrial permeability transition pore (mPTP) opening, which compromises mitochondrial function by eliminating membrane electrochemical potential and increasing reactive oxygen species.33 Therefore, mPTP opening in response to HAND-relevant stimuli, oxidative stress, and ARV drugs was monitored using a fluorescent live mitochondrial transition pore assay (Figure 6). Astrocytes were stained with the nuclear indicator Hoechst (blue), the mitochondrial dye mitotracker red (MTR) and calcein-AM, a membrane permeable fluorophore that diffuses freely into mitochondria and is quenched by cobalt chloride in the cytoplasm. Using live-cell fluorescent imaging, calcein and MTR labeling were measured in astrocytes (Figure 6a) treated with H2O2 (200 μM, Figure 6b), IL-1β (20 ng/ml, Figure 6c), HIV-1 (p24, 20 ng/ml, Figure 6d), TNF-α (50 ng/ml, Figure 6e), IL-1β+HIV-1+TNF-α together (Figure 6f), abacavir (4 μM, Figure 6g), Th (100 nM, Figure 6h), and DMSO (vehicle for Th, Figure 6i). Untreated and vehicle-treated astrocytes exhibited calcein (green) and MTR (red) colocalization in mitochondria (yellow; Figures 6a and i, arrows), reflecting closed mPTP. Calcein fluorescence was decreased in astrocytes treated with H2O2 and other HAND-relevant stimuli (Figures 6b–h), indicating mitochondrial pore opening (Figure 6, arrowhead). Together, these data show that HAND-relevant stimuli deleteriously affected astrocytes by promoting mPTP opening and loss of mitochondrial membrane integrity.
Intracellular calcium chelation inhibits abacavir- and IL-1β-mediated ER stress and subsequent mitochondrial damage in human astrocytes
To examine the effects of IL-1β- and abacavir-induced calcium release on ER stress and mPTP opening, astrocytes were pre-treated with the calcium chelator, 1,2-bis (2-aminophenoxy) ethane-N,N,N',N'-tetraaceticacid (acetoxymethyl ester) (BAPTA-AM). Consistent with Figures 1 and 2, BiP was significantly increased with IL-1β and abacavir alone (**P<0.01, ***P<0.001; Figure 7a). In parallel, BAPTA-AM pre-treatment successfully decreased IL-1β- and abacavir-induced BiP expression (###P<0.001; Figure 7a). To identify the consequences of elevated [Ca2+]i on mitochondrial membrane integrity, live-cell fluorescent imaging for calcein-AM (green) and MTR (red) was performed. Loss of calcein (green) and increase in MTR (red) fluorescence were observed in HIV-1-, IL-1β-, and abacavir-treated astrocytes (Figures 7d, f and h). However, BAPTA-AM pre-treatment preserved mitochondrial integrity as indicated by calcein fluorescence (green) in control and HAND-relevant stimuli-treated astrocytes (Figures 7b, c, e, g and i). These results demonstrate that IL-1β- and abacavir-induced ER stress and mPTP opening are highly calcium-dependent.
Neurological impairments continue to be a major health concern for HIV-infected patients in the post-ART era.1 Nevertheless, indirect causes and targetable mechanisms of neuronal degeneration in HAND are not well understood. ER stress is prevalent in several neurodegenerative diseases, though its regulation and contributions to neuropathogenesis have not been well studied in HAND.8,9 Aiming for a better understanding of HIV-1-induced UPR activation, the present study is focused on CNS neuroglial cells, that is, astrocytes, with various HAND-relevant stimuli (HIV-1, ARV drugs, and inflammation). Our results demonstrate that HAND-relevant stimuli induce ER stress and activate all three UPR pathways: PERK, IRE1α, and ATF6 in human astrocytes. Further, astrocyte intracellular calcium is elevated by IL-1β and abacavir via ER calcium release, which, when prolonged, triggers ER stress responses and mitochondrial depolarization. We also document elevated AEG-1 expression that positively correlates with ART-mediated ER stress. AEG-1 colocalization and interaction with calnexin implicate AEG-1 as a scaffolding protein regulating calcium signaling and ER function.
Ongoing low-level CNS viral replication and HIV-1-induced inflammation contribute to HAND.3,
Our findings demonstrate that HAND-associated inflammation induce ER stress in astrocytes. ER stress may be both a trigger and consequence of inflammation in many chronic inflammatory diseases.36 According to recent studies, ER stress-induced UPR signaling is associated with the production of many proinflammatory molecules.37 All three UPR pathways transcriptionally regulate the expression of inflammatory molecules through NF-κB and activator protein.36,38,39 Our study identifies IL-1β as a strong initiator of ER stress and the UPR in astrocytes, highlighting cross talk between ER stress and inflammation during HIV-1 CNS infection.
Recently, the CNS penetrance of ARV drugs has become increasingly clinically significant as the battle to reduce HIV-1-mediated neurotoxicity.40 However, long-term ART is associated with a range of adverse effects, including neuropathy, hyperbilirubinemia, lipodystrophy, neuropsychiatric disorders, retinal lesions, and hypersensitivity.41 ARV drugs triggered adverse side effects and toxicities, including, but not limited to, alterations in lipid and protein metabolism, insulin resistance, mitochondrial toxicity, oxidative stress, and neuronal damage.25,26 An in vitro study evaluated the neurotoxic effects of several ARV drugs on rat forebrain neuronal cultures. Out of the various ARV classes tested, NRTIs, including abacavir, showed high neurotoxicity.42 Therefore, another possible contributor to HAND is ARV drug-related neurotoxicity.
Our results demonstrate increased mRNA levels of ER chaperones, BiP and CHOP, with HAND-relevant stimuli, indicating ER stress in primary human astrocytes. While the UPR elevates BiP and CHOP expression, each has an opposing role in the outcome of the ER stress response. As a pro-survival protein, BiP removes ER misfolded proteins; whereas CHOP promotes apoptosis by favoring mitochondrial depolarization, cytochrome c release, and caspase 3 activation.43 Thus, the cell fate depends on the critical balance between BiP and CHOP.44 Initially, HAND-relevant stimuli significantly upregulated both BiP and CHOP. At later time points, BiP expression was decreased (data not shown), indicating that the disrupted balance between these two proteins may lead to cell death or apoptosis. Furthermore, cortical autopsy tissues from HIV-1-infected patients showed upregulated ER stress markers BiP and ATF6 in various CNS cell types, including neurons and astrocytes.14,45 Therefore, further investigation of ER stress-associated neurotoxic mechanisms of ARV drugs alone or in combination is warranted.
ER stress can induce three independent UPR signaling pathways: PERK, IRE1α, and ATF6. Elevation of all proximal sensors and downstream transcriptional factors suggests that all three UPR pathways regulate HAND-associated ER stress in astrocytes. In addition, IL-1β and abacavir increased eIF2α phosphorylation, indicating general attenuation of protein translation; a strategy to decrease the load of newly synthesized proteins in the ER lumen. However, UPR activation of ERSE-binding transcription factors, including ATF4, XBP-1s, and ATF6, upregulates compensatory expression of ER stress regulatory proteins, including BiP and CHOP.
One study evaluated AEG expression, including AEG-1 and AEG-9 (a.k.a. calnexin), following HIV-1 infection or treatment with gp120 in astrocytes.46 Recently, we identified AEG-1 as a novel modulator of HIV-1-associated neuroinflammation and glutamate clearance in astrocytes, suggesting a significant role in HAND.20,21 Therefore, we investigated plausible AEG-1 contributions toward HIV-1/ART-induced ER stress in astrocytes. The present study identifies AEG-1 as an ER stress inducible gene in astrocytes. To our knowledge, this is the first report to recognize AEG-1 as an interacting partner of calnexin, and reinforces AEG-1 as a scaffolding protein regulating ER calcium signaling through formation of multi-protein complexes.
ER harbors an intracellular calcium pool, which regulates essential cellular functions via calcium signaling. The present study demonstrates that HAND-relevant stimuli increase intracellular calcium in astrocytes. In addition, other studies have shown that HIV-1 proteins disrupt neuronal calcium homeostasis during HIV-1 encephalitis.47,48 Many ER calcium-binding proteins, including calreticulin, calnexin, BiP, and GRP94 have large calcium-binding capacities and regulate ER calcium homeostasis. Increased calnexin expression supports the theory that HAND-relevant stimuli fluctuate ER calcium in astrocytes. Severe disruption of ER calcium homeostasis also triggers ER stress and UPR signaling pathways to upregulate ER stress markers.49 Our study also shows upregulated expression of calcium-binding chaperones such as BiP. However, in addition to its chaperone function, BiP also has an important role in the intraluminal storage of calcium.50
The ER serves as the principal calcium store in the cells, and dynamic calcium transfer through ER–mitochondria contact sites leads to various cellular coordinated responses. Calcium-induced mPTP opening and permeabilization of mitochondrial membrane are the key events in early apoptosis.51 Prolonged mPTP opening has a crucial role in the pathogenesis of several diseases.52 Intracellular calcium chelation significantly reduced mPTP opening, suggesting that HAND-relevant stimuli-induced calcium influx into mitochondrial matrix causing mitochondrial dysfunction. Further, increased intracellular calcium can also induce calcium-dependent exocytosis, leading to excessive glutamate release from astrocytes.53 Other studies also support this conclusion as buffering of intracellular calcium reduced glutamate release in astrocytes.54 Excessive synaptic glutamate causes excitatory neurotransmission resulting in neuronal damage.
Taken together, HIV-1-associated inflammation and ART lead to ER stress and activation of UPR signaling in astrocytes. Our findings in the present study for the first time demonstrate that IL-1β and the NRTI abacavir induce intracellular calcium dysregulation, ER stress, AEG-1 expression, and mitochondrial dysfunction (mPTP opening) in astrocytes (Figure 8). In addition to deciphering these outcomes as independent correlates of HAND-relevant astrocyte activation, our studies also delineated the temporal order of these events and their concerted roles in astrocyte ER stress as summarized in Figure 8. We propose that in the post-ART era, chronic UPR activation and associated ER stress in astrocytes likely have key roles in mediating neurotoxicity in HIV-1-infected patients. In particular, these findings uncover astrocyte ER stress as a unique opportunity to explore novel therapeutic targets during HIV-1-associated neuropathogenesis.
Materials and methods
Isolation, cultivation, and treatment of primary human astrocytes
Human astrocytes were isolated from first- and early second-trimester-aborted specimens as previously described.55 Tissues were obtained in full compliance with ethical guidelines of the University of Washington, the University of North Texas Health Science Center, and the National Institutes of Health. Briefly, brain tissues were dissected and mechanically dissociated. Cell suspensions were centrifuged, washed, suspended in media, and plated at a density of 20-50×106 cells/150 cm2. Adherent astrocytes underwent several passages to enhance the purity of replicating astroglial cells before experimental use. The astrocyte preparations were routinely >99% pure as measured by immunocytochemical staining for GFAP and microglial marker CD68 to determine possible microglial contamination and contribution of microglia in inflammatory responses. Astrocytes were treated with IL-1β (20 ng/ml, R&D Systems, Minneapolis, MN, USA); HIV-1DJV (p24, 20 ng/ml); TNF-α (50 ng/ml, R&D Systems); ER stress compounds, Th (0.2 nM, Cell Signaling, Baltimore, MD, USA), Tm (1 μg/ml, Cell Signaling), and Bf (0.5 μg/ml, Cell Signaling); ARV drugs: abacavir (4 μM, ChemPacific, Baltimore, MD, USA), saquinavir (22.5 μM, ChemPacific), delavirdine (22.5 μM, ChemPacific), lopinavir (0.015 μM, ChemPacific), darunavir (5 nM, ChemPacific), lamivudine (11 μM, ChemPacific), stavudine (2.25 μM, ChemPacific), nevirapine (0.1 μM, ChemPacific), and ritonavir (0.1 μM, ChemPacific); and the calcium chelator BAPTA-AM (25 μM, Sigma-Aldrich, St Louis, MO, USA) at 37 °C and 5% CO2. HIV-1DJV was originally isolated from monocyte cultivation from a HIV-1-demented human brain tissue and was subsequently expanded in culture in peripheral blood monocytes.56
RNA extraction and gene expression analyses
Astrocyte RNA was isolated 8 h post treatment as described previously.57 RNA was reverse transcribed into cDNA as per the manufacturer’s instructions, and gene expression was assayed by RT2-PCR. Taqman 5′ nuclease RT2-PCR was performed using StepOnePlus detection system (Thermo Fisher Scientific, Waltham, MA, USA). Commercially available TaqMan gene expression assays were used to measure PERK (catalog no. HS00984006_m1), IRE1α (catalog no. Hs00176385_m1), ATF6 (catalog no. Hs00232586_m1), BiP (Hs00607129_gH), CHOP (catalog no. Hs00358796), calnexin (catalog no. Hs01558409_m1), AEG-1 (catalog no. Hs00757841_m1), and GAPDH (catalog no. 4310884E, Thermo Fisher Scientific) mRNA. GAPDH, a ubiquitously expressed housekeeping gene, was used as an internal normalizing control. The 25 μl reactions were carried out at 48 °C for 30 min, 95 °C for 10 min, followed by 40 cycles of 95 °C for 15 s and 60 °C for 1 min in 96-well optical, RT2-PCR plates. Transcripts were quantified by the comparative ΔΔCT method and represented as fold change to control.
Western blot analyses
Astrocytes were cultured as adherent monolayers in 75 cm2 flasks at a density of 8×106 cells/flask and allowed to recover for 24 h. Following recovery, cells were treated for various time points, and whole-cell protein extracts were isolated using mammalian protein extraction buffer (Thermo Fisher Scientific). Cells were collected by scraping in sterile ice-cold PBS to avoid alteration of protein expression on surface of cell membranes. Whole-cell protein extracts (25 μg) were boiled with 4× NuPAGE loading sample buffer at 100 °C for 5 min, resolved by Bolt 4–12% bis tris gel and subsequently transferred to nitrocellulose membranes using i-Blot (Thermo Fisher Scientific). The membranes were incubated with antibodies against ATF4 (1 : 1000, Cell Signaling), ATF6 (1 : 1000, Cell Signaling), XBP-1s (1 : 1000, Cell Signaling), p-eIF2α, and eIF2α (1 : 1000, Cell Signaling) overnight at 4 °C, washed, and then incubated with anti-rabbit IgG conjugated to horseradish peroxidase (1 : 10 000, Bio-Rad, Hercules, CA, USA) or anti-mouse IgG conjugated to horseradish peroxidase (1 : 10 000, Bio-Rad) for 2 h at room temperature. The membranes were then developed with SuperSignal west femto substrate (Thermo Fisher Scientific) and imaged using Fluorochem HD2 imager (ProteinSimple, San Jose, CA, USA). GAPDH (1 : 2000, Santa Cruz Biotechnology, Dallas, TX, USA) was used as a loading control.
Astrocytes were cultured as adherent monolayers at a density of 0.1×106 cells/well. Cultured cells were fixed after 24 h treatment with ice-cold acetone:methanol (1 : 1) solution for 20 min at −20 °C and blocked with blocking buffer (2% BSA in 1× PBS containing 0.1% Triton X-100) for 1 h at room temperature. Cells were then incubated with primary antibodies specific to calnexin (1 : 500, Cell Signaling), GFAP (1 : 400, Covance Inc., Princeton, NJ, USA) in blocking buffer overnight at 4 °C, washed, and incubated with AlexaFluor secondary antibodies, anti-rabbit (488 nm), and anti-chicken (594 nm; 1 : 100, Thermo Fisher Scientific). Micrographs were obtained on an ECLIPSE Ti-4 using the NIS-Elements BR. 3.2 software (Nikon, Minato, Tokyo, Japan).
Transfection of astrocytes
Cultured human astrocytes were transfected with pGP-CMV-GCaMP6s, a gift from Douglas Kim (Addgene, Cambridge, MA, USA; plasmid # 40753)29 using the Amaxa P3 primary cell 96-well kit, nucleofector and shuttle attachment (Lonza, Walkersville, MD, USA) according to the modified, manufacturer’s instructions. Briefly, 1.6×106 astrocytes were suspended in 20 μl nucleofector solution containing GCaMP6s (0.5 μg) and were electroporated using shuttle protocol CL133. Transfected cells were supplemented with astrocyte media and incubated for 30 min at 37 °C before plating into six channel μ-slides (0.4 VI, ibidi, Madison, WI, USA) at 1×105/channel. Cells were allowed to recover for 48 h before confocal imaging. Minimums of three channels were imaged from each biological astrocyte donor per treatment condition.
For colocalization studies, human non-transfected or transfected astrocytes were cultured on glass-bottom 48-well tissue culture plates (MatTek Corp., Ashland, MA, USA) at 1×105 cells/well in astrocyte media for 48 h. Cells were then treated for 24 h and carefully fixed before staining with antibodies specific to AEG-1 (1 : 200, Thermo Fisher Scientific) and calnexin as described in ICC. Before live-cell calcium imaging, astrocytes in μ-slides were briefly washed with PBS and supplemented with phenol red-, calcium-, and magnesium-free Hank’s buffered saline solution at 37 °C. Time-lapse micrographs were acquired every 500 ms for 6 min from astrocytes treated with IL-1β (20 ng/ml), abacavir (4 μM), and ionomycin (10 μM) at 10 s. Micrographs were obtained on Carl Zeiss LSM (Jena, Germany). The objective used was ×20 Plan-Apochromat, 0.8 NA, 0.55 mm WD. Photomultiplier tube detection was used with an excitation of 450–490 nm and emission of 593–668 nm. Colocalization, live-cell video imaging, and histogram analyses were performed using FujiFilm, ImageJ software; Version: 2.0.0-rc-41/1.5d (Fuji, Minato, Tokyo, Japan). Change in fluorescence was calculated by the following equation: ΔF=(F−F0)/(Fmax−F0), where F is the fluorescence intensity at any given time, F0 is the baseline fluorescence intensity, and Fmax is the maximum fluorescence intensity when exposed to ionomycin (10 μM).
Mitochondrial permeability transition pore
Astrocytes were cultured in 96-well plates at 0.05×106 cells/well. After 24 h treatment, the calcein/cobalt chloride quenching technique was used to elucidate mPTP opening using image-iT LIVE mitochondrial transition pore assay kit (Thermo Fisher Scientific). Live cells were imaged with appropriate excitation and emission filters for fluorescein on ECLIPSE Ti-4 using the NIS-Elements BR. 3.2 software (Nikon). In closed mPTP condition, cobalt quenches calcein fluorescence not sequestered in mitochondria; therefore, colocalization of MTR reflected as green/yellow for mitochondria.
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The present study was supported by R01MH087345 from NIMH to AG and the JES Edwards Foundation. We appreciate the assistance of the Laboratory of Developmental Biology for providing human brain tissues; also, supported by NIH award number 5R24 HD0008836 from the Eunice Kennedy Shriver National Institute of Child Health & Human Development. We also appreciate Ms. Lin Tang and Ms. Satomi Stacy for providing consistent high-quality primary astrocyte cultures, and Ms. Kathleen Borgmann for critical reading and editing of the manuscript. Dr. Richa Pandey assisted in mPTP experiments. Ms. I-Fen Chang provided technical assistance for all confocal imaging.