Next Article in Journal
Release of Anti-Inflammatory Palmitoleic Acid and Its Positional Isomers by Mouse Peritoneal Macrophages
Next Article in Special Issue
STAT3 Signalling via the IL-6ST/gp130 Cytokine Receptor Promotes Epithelial Integrity and Intestinal Barrier Function during DSS-Induced Colitis
Previous Article in Journal
Obesity and Diabetes: A Sword of Damocles for Future Generations
Previous Article in Special Issue
Javamide-II Inhibits IL-6 without Significant Impact on TNF-alpha and IL-1beta in Macrophage-Like Cells
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Biomedicines
Volume 8
Issue 11
10.3390/biomedicines8110479
biomedicines-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

β-Catenin Regulates Wound Healing and IL-6 Expression in Activated Human Astrocytes

by
Venkata Viswanadh Edara
1,2,†,‡,§,
Shruthi Nooka
2,‖,
Jessica Proulx
1,
Satomi Stacy
1,
Anuja Ghorpade
2,¶,** and
Kathleen Borgmann
1,2,*
1
Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX 76107, USA
2
Department of Microbiology, Immunology and Genetics, University of North Texas Health Science Center, Fort Worth, TX 76107, USA
*
Author to whom correspondence should be addressed.
†
Current affiliation: Department of Pediatrics, Division of Infectious Disease, Emory University School of Medicine, Atlanta, GA 30322, USA.
‡
Current affiliation: Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30329, USA.
§
Current affiliation: Yerkes National Primate Research Center, Atlanta, GA 30329, USA.
‖
Current affiliation: Internal Medicine Department, Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Current affiliation: Albany College of Pharmacy and Health Sciences, Albany, NY 12208, USA.
**
Current affiliation: Medical Innovation Collaborative of North Texas, Dallas, TX 75244, USA.
Biomedicines 2020, 8(11), 479; https://0-doi-org.brum.beds.ac.uk/10.3390/biomedicines8110479
Submission received: 1 October 2020 / Revised: 29 October 2020 / Accepted: 3 November 2020 / Published: 6 November 2020
(This article belongs to the Special Issue The Interleukin-6 Family in Disease Pathogenesis and Therapy)
Browse Figures
Review Reports Versions Notes

Abstract

:
Reactive astrogliosis is prominent in most neurodegenerative disorders and is often associated with neuroinflammation. The molecular mechanisms regulating astrocyte-linked neuropathogenesis during injury, aging and human immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) are not fully understood. In this study, we investigated the implications of the wingless type (Wnt)/β-catenin signaling pathway in regulating astrocyte function during gliosis. First, we identified that HIV-associated inflammatory cytokines, interleukin (IL)-1β and tumor necrosis factor (TNF)-α induced mediators of the Wnt/β-catenin pathway including β-catenin and lymphoid enhancer-binding factor (LEF)-1 expression in astrocytes. Next, we investigated the regulatory role of β-catenin on primary aspects of reactive astrogliosis, including proliferation, migration and proinflammatory responses, such as IL-6. Knockdown of β-catenin impaired astrocyte proliferation and migration as shown by reduced cyclin-D1 levels, bromodeoxyuridine incorporation and wound healing. HIV-associated cytokines, IL-1β alone and in combination with TNF-α, strongly induced the expression of proinflammatory cytokines including C-C motif chemokine ligand (CCL)2, C-X-C motif chemokine ligand (CXCL)8 and IL-6; however, only IL-6 levels were regulated by β-catenin as demonstrated by knockdown and pharmacological stabilization. In this context, IL-6 levels were negatively regulated by β-catenin. To better understand this relationship, we examined the crossroads between β-catenin and nuclear factor (NF)-κB pathways. While NF-κB expression was significantly increased by IL-1β and TNF-α, NF-κB levels were not affected by β-catenin knockdown. IL-1β treatment significantly increased glycogen synthase kinase (GSK)-3β phosphorylation, which inhibits β-catenin degradation. Further, pharmacological inhibition of GSK-3β increased nuclear translocation of both β-catenin and NF-κB p65 into the nucleus in the absence of any other inflammatory stimuli. HIV+ human astrocytes show increased IL-6, β-catenin and NF-κB expression levels and are interconnected by regulatory associations during HAND. In summary, our study demonstrates that HIV-associated inflammation increases β-catenin pathway mediators to augment activated astrocyte responses including migration and proliferation, while mitigating IL-6 expression. These findings suggest that β-catenin plays an anti-inflammatory role in activated human astrocytes during neuroinflammatory pathologies, such as HAND.

Graphical Abstract

1. Introduction

More than 30% of human immunodeficiency virus-1 (HIV-1) positive patients develop disorders associated with the central nervous system (CNS) [1,2]. Despite effective antiretroviral therapy (ART), HIV-1 invades the brain and causes neurological impairment, commonly referred to as HIV-associated neurocognitive disorders (HAND). Even in the post-ART era, low-level viral replication, HIV-1-associated neuroinflammation and oxidative stress contribute to neuropathogenesis [3,4], which highlights the significant need for identifying indirect host-regulated mechanisms for HAND adjunctive therapy.
Astrocytes, the most abundant glial cell in the brain, maintain CNS homeostasis and blood-brain barrier (BBB) integrity [5,6]. Reactive astrogliosis is a process where astrocytes respond to CNS insults, including infection, trauma, ischemia and neurodegeneration. Reactive astrocytes secrete a wide variety of pro- and anti-inflammatory factors that can potentially mediate neuroprotective or neurotoxic effects depending upon the severity, type, context and duration of the insult [7,8,9]. The severity of HAND is strongly associated with astrocyte dysfunction and immune activation. Inflammation mediates CNS damage and is a major contributor to HAND in HIV-infected individuals. Furthermore, HIV-1 infected microglia and perivascular macrophages, release various inflammatory and neurotoxic factors [10,11]. Several inflammatory cytokines including tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and IL-6 are elevated in the CNS or cerebrospinal fluid of HAND individuals [10,12,13,14]. Multiple studies have shown upregulation of inflammatory cytokines such as C-X-C motif chemokine ligand (CXCL)8, C-C motif chemokine ligand (CCL)2, CCL3, interferon (IFN)-γ and IL-6 production by astrocytes in response to macrophage-derived IL-1β and TNF-α during HIV-1 CNS infection [15,16,17,18]. These cytokines indirectly mediate their neurotoxic effects by activating astrocytes and play an important role in the further induction of neuronal injury and HAND pathogenesis [19,20,21,22].
The canonical wingless type Wnt (Wnt/β-catenin) signaling pathway is an important intracellular signal transduction pathway that promotes cell survival, differentiation, proliferation and communication. It is implicated in several neurodegenerative diseases including Alzheimer’s disease, Parkinson’s disease and neurological complications of acquired immunodeficiency syndrome [23,24,25,26]. Wnt/β-catenin pathway signaling restricts the HIV life cycle in target cell types, including peripheral blood mononuclear cells (PBMC) and astrocytes [27,28]. Wnt ligands are specifically upregulated in spinal cord dorsal horns of HIV+ patients with chronic pain, suggesting a critical role in pathogenesis of HIV-associated pain [29,30]. A hallmark of the Wnt/β-catenin pathway is the stabilization of cytosolic β-catenin, which translocates to the nucleus and activates the transcription of Wnt target genes [31]. Glycogen synthase kinase (GSK)-3β is highly active, which phosphorylates and degrades β-catenin through proteosomal degradation. GSK-3β has constitutive kinase activity, which is often negatively regulated through posttranslational modifications. In contrast, inactivation of GSK-3β activity inhibits β-catenin degradation. GSK-3β, as an upstream regulator of β-catenin, has been shown to play a major role in neuroinflammation in several neurodegenerative diseases [32,33,34].
The nuclear factor (NF)-κB signaling cascade is a pivotal modulator of inflammation and regulates innate and adaptive immune responses, cell proliferation, and apoptosis in various cell types [35,36]. While basal NF-κB activity is generally low in astrocytes, it increases significantly during inflammation, injury or disease [37,38,39,40]. Crosstalk between Wnt/β-catenin and NF-κB signaling during inflammation in various peripheral cell types was well summarized by Ma et al. [41]; however, little is known about the contribution of this crosstalk to the neuroinflammatory responses during astrogliosis. In the present study, we investigated the regulatory mechanisms mediated by Wnt/β-catenin signaling in the neuroinflammation-associated reactive astrogliosis process.

2. Experimental Section

2.1. Isolation, Culture and Treatment of Human Astrocytes

Human astrocytes were isolated from brain tissues recovered from first- and early second-trimester conceptual tissue as described previously [42,43,44]. Tissue samples were obtained from the Birth Defects Research Laboratory at the University of Washington in Seattle in full compliance with the ethical guidelines of the National Institutes of Health (NIH), Universities of Washington and North Texas Health Science Center. Our study involved the generation of human neural cells, hence it was reviewed by the North Texas Regional IRB and was found to be exempt under the provision of Title 45 of the Code of Federal Regulations part 46. 104 (d) (ii) wherein the biospecimens were de-identified and the researchers had no contact with subjects and could not re-identify the biospecimens. Isolated astrocytes were cultured in 1:1 v/v DMEM:F12 medium containing 10% fetal bovine serum (catalog no. PS-FB1 lot no. 27C1171, Peak Serum, Wellington, CO, USA) (catalog no. F-05000-D, lot no. F12C18D1, Atlas Biologicals, Fort Collins, CO, USA), penicillin 50 U-streptomycin 50 µg/mL-neomycin 100 μg/mL (PSN) (catalog no. P4083, Sigma Aldrich, St. Louis, MO, USA) and amphotericin B 2.5 μg/mL (catalog no. A2942, Sigma Aldrich). Astrocytes were plated either in 6-well plates or 150 cm2 flasks at 2 × 106 cells/well and 20 × 106 cells/flask, respectively, and treated with IL-1β (20 ng/mL, R&D Systems, Minneapolis, MN, USA), TNF-α (50 ng/mL, R&D Systems) and 6-bromoindirubin-3′-oxime (BIO) (500 nM, Millipore Sigma, Burlington, MA, USA) for 8 or 24 h at 37 °C and 5% CO2.

2.2. Transfection of Astrocytes

Human astrocytes were transfected either with no siRNA (mock), scrambled non-targeting siRNA (siCon, Dharmacon, Lafayette, CO, USA), or siRNA specific to β-catenin (siβ-catenin) using the AmaxaTM P3 primary cell 96-well nucleofector kit (Lonza, Walkersville, MD, USA). Briefly, 1.6 × 106 astrocytes were suspended in 20 μL nucleofector solution containing mock, siCon or siβ-catenin (200 nM) and transfected using a Nucleofector/Shuttle (Lonza) device. Transfected cells were supplemented with media and incubated for 20 min at 37 °C prior to plating. Cells were then cultured and allowed to recover for 48 h prior to experimental use. The knockdown efficiency of siβ-catenin was verified in all donors and averaged −88.5 ± 3.6% (±SD) as assayed by real-time polymerase chain reaction (RT-PCR) and −46.6 ± 3.9% by Western blot as described below.

2.3. In Vitro Scratch Assay

A well-established in vitro wound-healing model to study the migration of astrocytes was used [45]. Briefly, mock, siCon and siβ-catenin transfected human astrocytes were plated at a density of 2 × 106 cells per 6-well tissue culture plate well and grown to confluence for 48 h. The media was then aspirated, and a thin stretch of the confluent monolayer was scraped to create a “scratch or injury” using a sterile 10 μL pipette tip. Fresh astrocyte medium was added, and the wound was allowed to heal. The culture plates were examined periodically at 8, 24, 36 and 48 h and then returned to resume incubation. Live images of migrating cells were obtained using a phase contrast microscope (Zeiss Invertoskop 40C) (Carl Zeiss Microscopy, LLC, Thornwood, NY, USA).

2.4. Measures of Cell Viability

Metabolic activity of astrocytes was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT, Sigma Aldrich) assay as previously described [46]. Briefly, 0.25% MTT was added to astrocytes and incubated for 20 to 45 min at 37 °C. Then the MTT solution was removed, and crystals were dissolved in dimethyl sulfoxide (DMSO, Sigma Aldrich) for 15 min with gentle agitation. Absorbance was assayed at 490 nm in a SpectraMax M5 microplate reader (Molecular Devices, Sunnyvale, CA, USA).

2.5. Cell Proliferation/Bromodeoxyuridine (BrdU) Incorporation Assay

Transfected astrocytes were plated in triplicates in 96-well tissue culture plates at 5 × 104 cells/well and allowed to recover overnight. BrdU was added 12 h prior to the measurement of incorporation using BrdU Cell Proliferation Assay Kit (catalog no. 6813, Cell Signaling Technology, Inc., Danvers, MA, USA) as per the manufacturer’s instructions. Data were normalized to mock transfected astrocytes.

2.6. Quantification of Proinflammatory Cytokines by ELISA

Cell culture supernatants were collected at specified timepoints after treatment and used to quantify proinflammatory cytokines CXCL8, CCL2, and IL-6 (catalog no. D8000C, DCP00, and D6050, respectively, Quantikine ELISA Kits, R&D Systems). Assays were performed as per the manufacturer’s instructions and normalized to MTT levels.

2.7. Real Time Gene Expression Analysis

RNA was isolated using Trizol reagent (Thermo Fisher Scientific, Waltham, MA, USA) as previously described [42] followed by DNA digestion and precipitation. A Nanodrop fluorospectrometer (Thermo Fisher Scientific) was used to assess RNA purity and to quantify total RNA levels. Then, transcripts were made into cDNA as per the manufacturer’s instructions (High Capacity cDNA Reverse Transcription Kit, catalog no. 4368814, Thermo Fisher Scientific). Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (Thermo Fisher Scientific) was used as an internal control. Expression levels of β-catenin, LEF-1, IL-6, CXCL8, CCL2 and GAPDH were measured by RT-PCR using Taqman® gene expression assays (Table 1) and the StepOnePlus detection system (Thermo Fisher Scientific). The 20 μL reactions were carried out at 60 °C for three min, 95 °C for three min, followed by 40 cycles of 95 °C for 15 s and 60 °C for one min in a 96-well optical RT-PCR plate (Thermo Fisher Scientific). Transcripts were quantified by the comparative ΔΔCT method and represented as fold changes compared to untreated controls.

2.8. Western Blot Analyses

Astrocytes were cultured as adherent monolayers in 25 cm2 flasks at a density of 4 × 106 cells/flask and allowed to recover for 24 h. Following recovery, cells were treated with IL-1β (20 ng/mL) for 5, 15, 30, and 45 min. Cells were harvested by scraping in sterile ice-cold PBS to avoid alteration of protein expression on the surface of cell membranes. Cell lysate proteins (15 μg) were boiled with 4X NuPAGE lithium dodecyl sulfate loading sample buffer at 100 °C for 5–10 min, resolved by Bolt 4–12% bis tris gel, and subsequently transferred to nitrocellulose membranes using i-Blot (Life Technologies, Carlsbad, CA, USA). The membranes were incubated with antibodies against β-catenin (Cell Signaling Technology, Inc.), GSK-3β (Cell Signaling Technology, Inc.), p-GSK-3β (Cell Signaling Technology, Inc.), or GAPDH (Santa Cruz Biotechnology, Dallas, TX, USA) overnight at 4 °C, washed and then incubated with anti-mouse IgG or anti-rabbit IgG conjugated to horseradish peroxidase (1:10,000, Bio-Rad, Hercules, CA, USA) for 2 h at room temperature. The membrane was then developed with SuperSignal West Femto Substrate (Thermo Fisher Scientific) and imaged in a Flourochem HD2 Imager (ProteinSimple, San Jose, CA, USA). Densitometric analyses were performed using AlphaView software (V3.4.0.0, ProteinSimple).

2.9. WES Analyses

Cytoplasmic and nuclear lysates were isolated using a nuclear and cytoplasmic extraction kit according to the manufacturer’s methods (NE-PER, Thermo Fisher Scientific). Protein concentrations were determined by the BCA protein assay kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. Protein (0.4 mg/mL) was loaded into WES capillaries, and columns were probed with antibodies for lamin A/C (mouse, catalog no. NBP-19324, lot no. 41815; WES 1:50, Novus Biologicals, Littleton, CO, USA), β-catenin, NF-κB, and GAPDH. The levels of specific proteins were determined by the WES capillary protein detection system (ProteinSimple) according to the manufacturer’s directions.

2.10. Statistical Analysis

Statistical analyses were performed using GraphPad Prism 8.3.1 (GraphPad software, San Diego, CA, USA). All numerical data were taken as mean ± standard error of the mean (SEM). All data were analyzed using student t-test, one-way, or two-way analysis of variance (ANOVA) with Tukey or Fisher’s least significant difference post-hoc tests for pair-wise comparisons. Differences were considered statistically significant at p ≤ 0.05.

2.11. Data Availability

The R/G-HIV-1 transcriptome data used for the Ingenuity Pathway Analysis (IPA) (version 01-14, Qiagen, Germantown, MD, USA) in this publication have been deposited in NCBI’s gene expression omnibus (GEO) and are accessible through GEO series accession number GSE141756 [47].

3. Results

3.1. IL-1β and TNF-α Induce Wnt/β-Catenin and NF-κB Signaling in Astrocytes

HIV-1 infection of macrophages and microglia in the CNS leads to cellular activation and secretion of neurotoxic cytokines such as IL-1β and TNF-α [10,11]. These cytokines activate astrocytes and play a key role in astrocyte-associated neuronal injury and HAND pathogenesis. To investigate how IL-1β and TNF-α affect Wnt/β-catenin and NF-κB signaling during HIV-associated neuroinflammation, human astrocyte cultures were exposed to the pro-inflammatory cytokines IL-1β (20 ng/mL) and TNF-α (50 ng/mL) for 8 h either alone or in combination. As a key member of the Wnt/β-catenin pathway, β-catenin mRNA levels were analyzed by RT-PCR. Both IL-1β and TNF-α significantly increased β-catenin transcription (Figure 1A). Levels of LEF-1, a key transcription factor and downstream modulator of the Wnt/β-catenin pathway, were also measured. LEF-1 mRNA levels were elevated by at least 80% regardless of treatment (Figure 1B). These cytokines also significantly increased the NF-κB transcription (Figure 1C). However, combined treatment did not further amplify gene expression of any factors tested. Together, these data show that IL-1β and TNF-α induce LEF-1 and β-catenin expression, suggesting activation of β-catenin signaling in human astrocytes, concurrent with NF-κB signaling.

3.2. β-Catenin Differentially Regulates LEF-1 and NF-κB Transcription in IL-1β and TNF-α-Activated Astrocytes

Crosstalk between Wnt/β-catenin and NF-κB signaling during inflammation in various peripheral cell types has been well summarized by Ma et al. [41]. However, the cross regulation between these two pathways has never been studied in human astrocytes in the context of HIV-associated neuroinflammation. Thus, to assess the crosstalk between Wnt/β-catenin and NF-κB signaling pathways, β-catenin was transiently knocked down in primary human astrocytes, and responses to the HAND-relevant cytokines IL-1β and TNF-α were tested (Figure 2). β-catenin specific siRNA decreased the mRNA levels of β-catenin by approximately 90% with or without IL-1β/TNF-α treatment (Figure 2A) when compared to mock and siCon. The transient knockdown of β-catenin was also evident at protein level (Figure 2D). While LEF-1 transcriptional changes were larger in transfected astrocytes than untransfected astrocytes, silencing β-catenin diminished IL-1β- and TNF-α-induced LEF-1 transcription. Yet, basal LEF-1 transcription was unchanged (Figure 2B). However, silencing β-catenin and LEF-1 did not affect NF-κB transcription (Figure 2C). Together, these data indicate that the Wnt/β-catenin pathway does not directly regulate NF-κB transcription in human astrocytes during HIV-associated inflammation.

3.3. β-Catenin Regulates Wound Healing and Astrocyte Proliferation

Wnt/β-catenin canonical pathway regulates cell proliferation, cell mobility and differentiation. To investigate the role of β-catenin signaling in astrocyte proliferation and migration following injury, either no siRNA (Mock), non-targeting siRNA (siCon) or siRNA specific for β-catenin (siβ-catenin) transfected astrocytes were plated, and a scratch was made following recovery. Wound sites were observed at defined time points to measure astrocyte migration. No difference in astrocyte migration was seen at 8 h in all conditions (Figure 3A1, B1, C1). However, β-catenin knockdown significantly reduced the migration of astrocytes to the injury site at 24 and 36 h (Figure 3C2 and C3, respectively) compared to mock and siCon transfected astrocytes (Figure 3A2, B2 and A3, B3, respectively). Scratched monolayers were completely closed after 48 h in both mock and siCon transfected astrocytes (Figure 3A4 and B4, respectively), leaving minor gaps in the wound of siβ-catenin transfected astrocytes (Figure 3C4).
Canonical Wnt/β-catenin pathway regulates the expression of several transcription factors such as c-myc, cyclin D1 and survivin that mediate cell proliferation [48]. To study the effects of β-catenin pathway on reactive astrogliosis, particularly cell proliferation in vitro, we measured cyclin D1 mRNA levels and BrdU incorporation in human astrocytes following β-catenin knockdown. Significant reductions in cyclin D1 mRNA levels were observed (Figure 3E) following β-catenin knockdown. Simultaneously β-catenin knockdown also resulted in significantly reduced BrdU incorporation, which is a direct measure of cell proliferation (Figure 3F). Together, these data indicate that β-catenin knockdown impairs astrogliosis, i.e., migration and proliferation of astrocytes during injury.

3.4. β-Catenin Negatively Regulates Astrocyte IL-6 Expression

To determine if β-catenin regulates neuroinflammation, siRNA transfected astrocytes were treated with IL-1β and TNF-α, and levels of CXCL8, CCL2 and IL-6 were measured at both mRNA and protein levels. IL-1β and TNF-α treatment significantly increased CXCL8 and CCL2 expression both at mRNA (data not shown) and protein levels (Figure 4A and B, respectively). Knockdown of β-catenin did not affect the protein levels of either CXCL8 or CCL2. Treatment with IL-1β and TNF-α also significantly increased IL-6 mRNA and protein levels (Figure 5A and B, respectively). However, IL-1β treatment increased IL-6 to a greater magnitude than TNF-α, and no synergistic effect of the combination treatment was apparent. Moreover, β-catenin knockdown significantly increased IL-1β-induced IL-6 expression alone and in combination with TNF-α, but did not significantly alter TNF-α-induced IL-6. To verify the opposite, the effects of β-catenin activation were also evaluated. Human astrocytes were pre-treated with BIO, a GSK-3β inhibitor that prevents proteasomal-mediated degradation of β-catenin, makes it readily available to translocate into the nucleus, and activates the canonical Wnt pathway. Pre-treated or untreated astrocytes were stimulated with IL-1β and TNF-α, and supernatants were assayed for IL-6 levels by ELISA (Figure 5C). While TNF-α minimally increased IL-6 levels, β-catenin stabilization did not affect TNF-α-induced IL-6 expression. However, in the context of IL-1β alone and in combination with TNF-α, β-catenin stabilization significantly decreased IL-6 secretion (Figure 5C). Together the data indicate that β-catenin negatively regulates IL-6 expression in human astrocytes when exposed to IL-1β alone or in combination with TNF-α.

3.5. Stabilization of β-Catenin Increases Nuclear Localization of NF-κB

Wnt/β-catenin signaling involves inhibition of GSK-3β kinase activity by phosphorylation at serine 9, permitting β-catenin accumulation and subsequent expression of Wnt target genes. Since GSK-3β activity is inhibited by phosphorylation at serine 9, we investigated GSK-3β phosphorylation following IL-1β stimulation. Astrocytes were treated with 20 ng/mL of IL-1β for various time points up to 45 min. IL-1β treatment significantly increased GSK-3β phosphorylation at 15 min through 45 min (Figure 6A,B). Data indicate that IL-1β increased the inhibitory phosphorylation of GSK-3β at serine 9, which promotes β-catenin stabilization mechanism in astrocytes.
To determine if activation of the Wnt/β-catenin signaling pathway regulates the nuclear localization of NF-κB, cells were treated with BIO, cytosolic and nuclear fractions of cell lysates were analyzed for β-catenin and NF-κB levels using simple WES. β-catenin stabilization slightly decreased cytosolic levels of both β-catenin and NF-κB (Figure 6C and D, respectively), which were coupled with increased translocation of both proteins into the nucleus (Figure 6E,F). Together our data indicate that activating the canonical Wnt/β-catenin signaling pathway significantly increased nuclear translocation of NF-κB in human astrocytes.

3.6. Molecular Interactions between GSK-3β, β-Catenin, NF-κB and IL-6 during HIVE and HAD

To examine the interrelationships in the context of HIV-infected astrocytes, we accessed a previously published dataset that quantified mRNA expression levels in Red/Green HIV + astrocytes [47]. Expression levels of the molecules of interest, GSK-3β, β-catenin, NF-κB, and IL-6 from the Red/Green-HIV-1 infected human astrocyte data were overlaid with HIV encephalitis (HIVE) and HIV-associated dementia (HAD) disease and biological function using IPA pathway explorer (Figure 7). This analysis indicates multiple pre-existing interactions between the molecules of interest as well as how these molecules interact and affect other molecules implicated in HIVE and HAD. Aligning with the IPA data knowledge, the illustration shows the upregulation of various neuroinflammatory cytokines such as CCL8, CCL2 and IL-6. The illustration also shows that β-catenin affects IL-6 expression both directly and indirectly, while NF-κB is connected to IL-6, CXCL8 and CCL2 as per the IPA curated knowledge. However, our studies demonstrated for the first time that β-catenin negatively regulates IL-6 expression in activated human astrocytes.

4. Discussion

In this study we investigated the implications of the Wnt/β-catenin signaling pathway in regulating astrocyte function in the context of HIV-associated neuroinflammation and gliosis. HIV-associated inflammation, IL-1β and TNF-α alone and in combination, strongly induced the expression of proinflammatory cytokines including CCL2, CXCL8 and IL-6 and showed significant activation of both the Wnt/β-catenin and NF-κB signaling pathways in primary human astrocytes. Knockdown of β-catenin impaired astrocyte proliferation and migration but only affected one of the three proinflammatory responses of astrocytes that we examined. IL-1β-induced IL-6 levels were increased by β-catenin knockdown and decreased with BIO, a β-catenin stabilizer, while CCL2 and CXCL8 remained unaffected by β-catenin knockdown. To better understand this relationship, we examined the crossroads between β-catenin and NF-κB pathways. While NF-κB levels were not affected by β-catenin knockdown, β-catenin stabilization increased translocation of both β-catenin and NF-κB p65 into the nucleus in the absence of any other inflammatory stimuli. Together, these data strongly indicate crosstalk between these two pathways in astrocytes during injury and neuroinflammation, wherein reactive astrocyte responses including migration and proliferation were augmented by β-catenin signaling, while the IL-6 response was mitigated. These findings suggest that β-catenin plays an anti-inflammatory role in activated human astrocytes during neuroinflammatory pathologies such as HAND (Figure 8).
At early stages of CNS insults, astrocytes migrate and form barriers at the injured site to restrict the spread of infectious agents or inflammatory cells [49,50]. The β-catenin pathway is a well-known signaling cascade that is involved in migration and the proliferation of several cancers. Initially, we investigated if injury-induced β-catenin signaling contributes to reactive astrocyte phenotype, i.e., proliferation and migration. Following injury, we identified knockdown of β-catenin altered migration of astrocytes to the wound site. The dynamics of β-catenin signaling and its regulation of cell cycle mediators, including cyclin D1 and c-myc expression, are well recognized [48,51]. We also demonstrated β-catenin regulation of cyclin D1 expression in astrocytes, which is essential for proliferation. Taken together, these findings indicate the significance of β-catenin in the proliferative and migration capacity of reactive astrocytes during neurodegenerative diseases.
While HIV-1 predominantly replicates in microglia and macrophages in the CNS, restrictively infected astrocytes were recently shown to be a reservoir that is capable of reinfecting the periphery [52]. Infected macrophages and microglia are the major source of cytokines such as IL-1β, TNF-α and IFN-γ. Apart from the intrinsic upregulation of NF-κB transcription during HIV-1 infection, macrophage-derived inflammatory cytokines, IL-1β and TNF-α, are known to activate NF-κB signaling and induce a reactive astrogliosis phenotype in astrocytes [53,54]. Our recent studies demonstrate that latently infected HIV+ astrocytes resemble actively infected astrocytes and take on a proinflammatory phenotype [47].
Reactive astrocytes release a wide variety of inflammatory mediators such as cytokines and chemokines that are both neuroprotective (cytokines such as IL-10 and transforming growth factor-β) and neurotoxic (such as IL-1β, CXCL8, CCL2 and TNF-α) in nature [49]. IL-1β is also known to activate the phosphoinositide 3-kinase (PI3K)/Akt/GSK-3β pathway in several cell types, such as hepatocytes, epithelial cells, airway and colonic smooth muscle cells [55,56]. Inhibitory serine-phosphorylation is the most frequent mechanism that regulates the activity of GSK-3β. Activated Akt, the product of the PI3K pathway, inactivates GSK-3β through phosphorylation, which leads to activation of canonical Wnt/β-catenin signaling. Our studies showed that HIV-associated inflammatory stimuli IL-1β and TNF-α significantly upregulated Wnt/β-catenin signaling and its downstream regulators in human astrocytes. This activation could be due to IL-1β and TNF-α-induced GSK-3β phosphorylation.
Crosstalk between NF-κB signaling and canonical Wnt/β-catenin signaling during inflammation has been extensively studied in the periphery, and has shown both positive and negative associations. Studies have demonstrated modulation of inflammatory responses via interaction of Wnt/β-catenin signaling with NF-κB in murine hepatocytes [57] and positive regulation of NF-κB activity by β-catenin in human bronchial epithelial cells following treatment with lipopolysaccharide. Proinflammatory cytokines, including IL-6, CXCL8, IL-1β, TNF-α and CCL2, were augmented [58]. In colorectal cancer cells, β-catenin regulates the activity of the NF-κB promoter [59], whereas inhibition of GSK-3β by lithium or siRNA potentiated TNF-induced expression of IL-6 and CCL2 in human microvascular endothelial cells [60].
Robinson et al. recently demonstrated how the Wnt/β-catenin pathway discordantly regulates IL-6 expression in naïve astrocytes [61]. Robust β-catenin expression decreased IL-6 promoter activity by interacting with T-cell factor (TCF)/LEF transcription factors, independent of NF-κB. However, they also showed that β-catenin augmented NF-κB and CCAAT/enhancer binding protein β expression to boost IL-6 expression [61]. In our studies, neither β-catenin knockdown nor stabilization with BIO altered total NF-κB p65 levels (data not shown). Yet, NF-κB translocation into the nucleus in the absence of astrocytes activation was augmented in concordance with their observations. Further, β-catenin knockdown did not significantly alter basal IL-6 expression in our primary human astrocytes, which was almost undetectable compared to activated levels. While in IL-1β and TNF-α activated astrocytes, the effects of β-catenin on IL-6 levels were significant. Both IL-1β and TNF-α have been shown to activate protein kinase C, which also plays a primary role in the stimulation of IL-6 gene expression in human astrocytes [62]. In this context, β-catenin-associated regulation of astrocyte responses to HIV and neuroinflammation are complex and likely dependent upon the type and gliosis status of these multi-functional cells.
Elevated plasma IL-6 levels have been associated with increased mortality and morbidity in people living with HIV even with effective retroviral suppression [63,64,65], making it a hallmark for HIV-associated inflammation. Early in the epidemic, IL-6 reportedly increased HIV-1 replication in several cell types such as PBMC, monocyte-derived macrophages, and U1 latently infected cells derived from U937 cells [66,67]. This pro-inflammatory cytokine induces B cell differentiation into immunoglobulin producing plasma cells and co-activates various subsets of T cells to mediate immunity. However, during HIV infection, IL-6 may also hinder the immune system by increasing memory T cell turnover and promoting thymic involution impairing T cell reconstitution [68]. In fact, HAND patients show elevated IL-6 levels in cerebrospinal fluid [69,70,71], which are associated with HIV compartmentalization and cognitive impairment. Activation of Wnt/β-catenin signaling, specifically transcription factors LEF-1/4 are known restrictive factors of HIV-1 replication and transcription in astrocytes [27]. NF-κB-induced IL-6 expression in astrocytes was shown to indirectly mediate HIV-associated complement 3 expression to promote neuroinflammation and cognitive impairment [39]. HIV-1 viral proteins such as glycoprotein (gp)120 or negative regulatory factor (Nef) treatment lead to IL-6 expression in human astrocytes, which is mediated by the NF-κB pathway [72,73]. Thus, astrocyte regulation of IL-6 production is an important aspect of HAND pathology and further investigations into these phenomena are warranted.

Author Contributions

Conceptualization, S.N. and A.G.; methodology, V.V.E. and S.N.; formal analysis, V.V.E., S.N. and J.P.; investigation, V.V.E., S.N., J.P., and S.S.; writing—original draft preparation, V.V.E., S.N. and J.P.; writing—review and editing, S.S., A.G. and K.B.; supervision, A.G. and K.B.; project administration and funding acquisition, A.G. and K.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by National Institute of Mental Health, grant number R21 MH113452 and the JES Edwards Foundation of Fort Worth. We appreciate the assistance of the Laboratory of Developmental Biology at UW in Seattle for providing human brain tissues, supported by NIH 5R24 HD0008836 from the Eunice Kennedy Shriver National Institute of Child Health and Human Development.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Heaton, R.K.; Clifford, D.B.; Franklin, D.R., Jr.; Woods, S.P.; Ake, C.; Vaida, F.; Ellis, R.J.; Letendre, S.L.; Marcotte, T.D.; Atkinson, J.H.; et al. Hiv-associated neurocognitive disorders persist in the era of potent antiretroviral therapy: Charter study. Neurology 2010, 75, 2087–2096. [Google Scholar] [CrossRef] [Green Version]
  2. Heaton, R.K.; Franklin, D.R.; Ellis, R.J.; McCutchan, J.A.; Letendre, S.L.; Leblanc, S.; Corkran, S.H.; Duarte, N.A.; Clifford, D.B.; Woods, S.P.; et al. HIV-associated neurocognitive disorders before and during the era of combination antiretroviral therapy: Differences in rates, nature, and predictors. J. Neurovirol. 2011, 17, 3–16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Spudich, S.; Gonzalez-Scarano, F. HIV-1-related central nervous system disease: Current issues in pathogenesis, diagnosis, and treatment. Cold Spring Harb. Perspect. Med. 2012, 2, a007120. [Google Scholar] [CrossRef] [Green Version]
  4. Louboutin, J.P.; Strayer, D. Role of Oxidative Stress in HIV-1-Associated Neurocognitive Disorder and Protection by Gene Delivery of Antioxidant Enzymes. Antioxidants 2014, 3, 770–797. [Google Scholar] [CrossRef]
  5. Alvarez, J.I.; Katayama, T.; Prat, A. Glial influence on the blood brain barrier. Glia 2013, 61, 1939–1958. [Google Scholar] [CrossRef] [Green Version]
  6. Lundgaard, I.; Osorio, M.J.; Kress, B.T.; Sanggaard, S.; Nedergaard, M. White matter astrocytes in health and disease. Neuroscience 2014, 276, 161–173. [Google Scholar] [CrossRef] [Green Version]
  7. Sofroniew, M.V.; Vinters, H.V. Astrocytes: Biology and pathology. Acta Neuropathol. 2010, 119, 7–35. [Google Scholar] [CrossRef] [Green Version]
  8. Li, K.; Li, J.; Zheng, J.; Qin, S. Reactive Astrocytes in Neurodegenerative Diseases. Aging Dis. 2019, 10, 664–675. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Colangelo, A.M.; Alberghina, L.; Papa, M. Astrogliosis as a therapeutic target for neurodegenerative diseases. Neurosci. Lett. 2014, 565, 59–64. [Google Scholar] [CrossRef] [Green Version]
  10. Brabers, N.A.; Nottet, H.S. Role of the pro-inflammatory cytokines TNF-alpha and IL-1beta in HIV-associated dementia. Eur. J. Clin. Investig. 2006, 36, 447–458. [Google Scholar] [CrossRef] [PubMed]
  11. Kaul, M.; Garden, G.A.; Lipton, S.A. Pathways to neuronal injury and apoptosis in HIV-1-associated dementia. Nature 2001, 410, 988–993. [Google Scholar] [CrossRef]
  12. Sharief, M.K.; Ciardi, M.; Thompson, E.J.; Sorice, F.; Rossi, F.; Vullo, V.; Cirelli, A. Tumour necrosis factor-alpha mediates blood-brain barrier damage in HIV-1 infection of the central nervous system. Mediat. Inflamm. 1992, 1, 191–196. [Google Scholar] [CrossRef]
  13. Perrella, O.; Guerriero, M.; Izzo, E.; Soscia, M.; Carrieri, P.B. Interleukin-6 and granulocyte macrophage-CSF in the cerebrospinal fluid from HIV infected subjects with involvement of the central nervous system. Arq. Neuropsiquiatr. 1992, 50, 180–182. [Google Scholar] [CrossRef]
  14. Achim, C.L.; Heyes, M.P.; Wiley, C.A. Quantitation of human immunodeficiency virus, immune activation factors, and quinolinic acid in AIDS brains. J. Clin. Investig. 1993, 91, 2769–2775. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Choi, S.S.; Lee, H.J.; Lim, I.; Satoh, J.; Kim, S.U. Human astrocytes: Secretome profiles of cytokines and chemokines. PLoS ONE 2014, 9, e92325. [Google Scholar] [CrossRef] [Green Version]
  16. Fields, J.; Ghorpade, A. C/EBPbeta regulates multiple IL-1beta-induced human astrocyte inflammatory genes. J. Neuroinflamm. 2012, 9, 177. [Google Scholar] [CrossRef] [Green Version]
  17. Suryadevara, R.; Holter, S.; Borgmann, K.; Persidsky, R.; Labenz-Zink, C.; Persidsky, Y.; Gendelman, H.E.; Wu, L.; Ghorpade, A. Regulation of tissue inhibitor of metalloproteinase-1 by astrocytes: Links to HIV-1 dementia. Glia 2003, 44, 47–56. [Google Scholar] [CrossRef] [Green Version]
  18. Borgmann, K.; Ghorpade, A. HIV-1, methamphetamine and astrocytes at neuroinflammatory Crossroads. Front. Microbiol. 2015, 6, 1143. [Google Scholar] [CrossRef] [Green Version]
  19. Kaul, M. HIV-1 associated dementia: Update on pathological mechanisms and therapeutic approaches. Curr. Opin. Neurol. 2009, 22, 315–320. [Google Scholar] [CrossRef] [Green Version]
  20. Gendelman, H.E.; Ghorpade, A.; Persidsky, Y. The neuropathogenesis of HIV-1 associated dementia. In In Defense of the Brain: Current Concepts in the Immunopathogenesis and Clinical Aspects of CNS Infections; Peterson, P.K., Remington, J.S., Eds.; Blackwell Science: Maiden, MA, USA, 1997; pp. 290–304. [Google Scholar]
  21. Ghorpade, A.; Holter, S.; Borgmann, K.; Persidsky, R.; Wu, L. HIV-1 and IL-1beta regulate Fas ligand expression in human astrocytes through the NF-kappaB pathway. J. Neuroimmunol. 2003, 141, 141–149. [Google Scholar] [CrossRef]
  22. Li, W.; Henderson, L.J.; Major, E.O.; Al-Harthi, L. IFN-gamma mediates enhancement of HIV replication in astrocytes by inducing an antagonist of the beta-catenin pathway (DKK1) in a STAT 3-dependent manner. J. Immunol. 2011, 186, 6771–6778. [Google Scholar] [CrossRef] [Green Version]
  23. Inestrosa, N.C.; Montecinos-Oliva, C.; Fuenzalida, M. Wnt signaling: Role in Alzheimer disease and schizophrenia. J. Neuroimmune Pharmacol. 2012, 7, 788–807. [Google Scholar] [CrossRef]
  24. Inestrosa, N.C.; Arenas, E. Emerging roles of Wnts in the adult nervous system. Nat. Rev. Neurosci. 2010, 11, 77–86. [Google Scholar] [CrossRef]
  25. Al-Harthi, L. Interplay between Wnt/beta-catenin signaling and HIV: Virologic and biologic consequences in the CNS. J. Neuroimmune Pharmacol. 2012, 7, 731–739. [Google Scholar] [CrossRef] [Green Version]
  26. Caricasole, A.; Bakker, A.; Copani, A.; Nicoletti, F.; Gaviraghi, G.; Terstappen, G.C. Two sides of the same coin: Wnt signaling in neurodegeneration and neuro-oncology. Biosci. Rep. 2005, 25, 309–327. [Google Scholar] [CrossRef] [PubMed]
  27. Narasipura, S.D.; Henderson, L.J.; Fu, S.W.; Chen, L.; Kashanchi, F.; Al-Harthi, L. Role of beta-Catenin and TCF/LEF Family Members in Transcriptional Activity of HIV in Astrocytes. J. Virol. 2012, 86, 1911–1921. [Google Scholar] [CrossRef] [Green Version]
  28. Wortman, B.; Darbinian, N.; Sawaya, B.E.; Khalili, K.; Amini, S. Evidence for regulation of long terminal repeat transcription by Wnt transcription factor TCF-4 in human astrocytic cells. J. Virol. 2002, 76, 11159–11165. [Google Scholar] [CrossRef] [Green Version]
  29. Shi, Y.; Shu, J.; Gelman, B.B.; Lisinicchia, J.G.; Tang, S.J. Wnt signaling in the pathogenesis of human HIV-associated pain syndromes. J. Neuroimmune Pharmacol. 2013, 8, 956–964. [Google Scholar] [CrossRef] [Green Version]
  30. Yuan, S.B.; Ji, G.; Li, B.; Andersson, T.; Neugebauer, V.; Tang, S.J. A Wnt5a signaling pathway in the pathogenesis of HIV-1 gp120-induced pain. Pain 2015, 156, 1311–1319. [Google Scholar] [CrossRef] [Green Version]
  31. Gordon, M.D.; Nusse, R. Wnt signaling: Multiple pathways, multiple receptors, and multiple transcription factors. J. Biol. Chem. 2006, 281, 22429–22433. [Google Scholar] [CrossRef] [Green Version]
  32. Jope, R.S.; Yuskaitis, C.J.; Beurel, E. Glycogen synthase kinase-3 (GSK3): Inflammation, diseases, and therapeutics. Neurochem. Res. 2007, 32, 577–595. [Google Scholar] [CrossRef] [Green Version]
  33. Maqbool, M.; Mobashir, M.; Hoda, N. Pivotal role of glycogen synthase kinase-3: A therapeutic target for Alzheimer’s disease. Eur. J. Med. Chem. 2016, 107, 63–81. [Google Scholar] [CrossRef] [PubMed]
  34. Golpich, M.; Amini, E.; Hemmati, F.; Ibrahim, N.M.; Rahmani, B.; Mohamed, Z.; Raymond, A.A.; Dargahi, L.; Ghasemi, R.; Ahmadiani, A. Glycogen synthase kinase-3 beta (GSK-3beta) signaling: Implications for Parkinson’s disease. Pharmacol. Res. 2015, 97, 16–26. [Google Scholar] [CrossRef] [PubMed]
  35. Gilmore, T.D. Introduction to NF-kappaB: Players, pathways, perspectives. Oncogene 2006, 25, 6680–6684. [Google Scholar] [CrossRef] [Green Version]
  36. Lawrence, T. The nuclear factor NF-kappaB pathway in inflammation. Cold Spring Harb. Perspect. Biol. 2009, 1, a001651. [Google Scholar] [CrossRef] [Green Version]
  37. Bhakar, A.L.; Tannis, L.L.; Zeindler, C.; Russo, M.P.; Jobin, C.; Park, D.S.; MacPherson, S.; Barker, P.A. Constitutive nuclear factor-kappa B activity is required for central neuron survival. J. Neurosci. 2002, 22, 8466–8475. [Google Scholar] [CrossRef] [PubMed]
  38. Schmidt-Ullrich, R.; Memet, S.; Lilienbaum, A.; Feuillard, J.; Raphael, M.; Israel, A. NF-kappaB activity in transgenic mice: Developmental regulation and tissue specificity. Development 1996, 122, 2117–2128. [Google Scholar]
  39. Nitkiewicz, J.; Borjabad, A.; Morgello, S.; Murray, J.; Chao, W.; Emdad, L.; Fisher, P.B.; Potash, M.J.; Volsky, D.J. HIV induces expression of complement component C3 in astrocytes by NF-kappaB-dependent activation of interleukin-6 synthesis. J. Neuroinflamm. 2017, 14, 23. [Google Scholar] [CrossRef] [Green Version]
  40. Gupta, A.S.; Waters, M.R.; Biswas, D.D.; Brown, L.N.; Surace, M.J.; Floros, C.; Siebenlist, U.; Kordula, T. RelB controls adaptive responses of astrocytes during sterile inflammation. Glia 2019, 67, 1449–1461. [Google Scholar] [CrossRef]
  41. Ma, B.; Hottiger, M.O. Crosstalk between Wnt/beta-Catenin and NF-kappaB Signaling Pathway during Inflammation. Front. Immunol. 2016, 7, 378. [Google Scholar] [CrossRef]
  42. Gardner, J.; Ghorpade, A. Tissue inhibitor of metalloproteinase (TIMP)-1: The TIMPed balance of matrix metalloproteinases in the central nervous system. J. Neurosci. Res. 2003, 74, 801–806. [Google Scholar] [CrossRef] [Green Version]
  43. You, Y.; Borgmann, K.; Edara, V.V.; Stacy, S.; Ghorpade, A.; Ikezu, T. Activated human astrocyte-derived extracellular vesicles modulate neuronal uptake, differentiation and firing. J. Extracell. Vesicles 2020, 9, 1706801. [Google Scholar] [CrossRef] [PubMed]
  44. Borgmann, K.; Gendelman, H.E.; Ghorpade, A. Isolation and HIV-1 infection of primary human microglia from fetal and adult tissue. Methods Mol. Biol. 2005, 304, 49–70. [Google Scholar]
  45. Liang, C.C.; Park, A.Y.; Guan, J.L. In vitro scratch assay: A convenient and inexpensive method for analysis of cell migration in vitro. Nat. Protoc. 2007, 2, 329–333. [Google Scholar] [CrossRef] [Green Version]
  46. Manthorpe, M.; Fagnani, R.; Skaper, S.D.; Varon, S. An automated colorimetric microassay for neuronotrophic factors. Brain Res. 1986, 390, 191–198. [Google Scholar] [CrossRef]
  47. Edara, V.V.; Ghorpade, A.; Borgmann, K. Insights into the Gene Expression Profiles of Active and Restricted Red/Green-HIV(+) Human Astrocytes: Implications for Shock or Lock Therapies in the Brain. J. Virol. 2020, 94. [Google Scholar] [CrossRef]
  48. Shtutman, M.; Zhurinsky, J.; Simcha, I.; Albanese, C.; D’Amico, M.; Pestell, R.; Ben-Ze’ev, A. The cyclin D1 gene is a target of the beta-catenin/LEF-1 pathway. Proc. Natl. Acad. Sci. USA 1999, 96, 5522–5527. [Google Scholar] [CrossRef] [Green Version]
  49. Sofroniew, M.V. Molecular dissection of reactive astrogliosis and glial scar formation. Trends Neurosci. 2009, 32, 638–647. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Sofroniew, M.V. Reactive astrocytes in neural repair and protection. Neurosci. Rev. J. Bringing Neurobiol. Neurol. Psychiatry 2005, 11, 400–407. [Google Scholar] [CrossRef] [PubMed]
  51. Kafri, P.; Hasenson, S.E.; Kanter, I.; Sheinberger, J.; Kinor, N.; Yunger, S.; Shav-Tal, Y. Quantifying beta-catenin subcellular dynamics and cyclin D1 mRNA transcription during Wnt signaling in single living cells. Elife 2016, 5. [Google Scholar] [CrossRef]
  52. Lutgen, V.; Narasipura, S.D.; Barbian, H.J.; Richards, M.; Wallace, J.; Razmpour, R.; Buzhdygan, T.; Ramirez, S.H.; Prevedel, L.; Eugenin, E.A.; et al. HIV infects astrocytes in vivo and egresses from the brain to the periphery. PLoS Pathog. 2020, 16, e1008381. [Google Scholar] [CrossRef] [PubMed]
  53. Han, Y.; He, T.; Huang, D.R.; Pardo, C.A.; Ransohoff, R.M. TNF-alpha mediates SDF-1 alpha-induced NF-kappa B activation and cytotoxic effects in primary astrocytes. J. Clin. Investig. 2001, 108, 425–435. [Google Scholar] [CrossRef]
  54. Zhao, M.; Kim, M.; Morgello, S.; Lee, S.C. Expression of inducible nitric oxide synthase, interleukin-1 and caspase-1 in HIV-1 encephalitis. J. Neuroimmunol. 2001, 115, 182–191. [Google Scholar] [CrossRef]
  55. Dragon, S.; Rahman, M.S.; Yang, J.; Unruh, H.; Halayko, A.J.; Gounni, A.S. IL-17 enhances IL-1beta-mediated CXCL-8 release from human airway smooth muscle cells. Am. J. Physiol. Lung Cell Mol. Physiol. 2007, 292, L1023–L1029. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Hu, W.; Li, F.; Mahavadi, S.; Murthy, K.S. Upregulation of RGS4 expression by IL-1beta in colonic smooth muscle is enhanced by ERK1/2 and p38 MAPK and inhibited by the PI3K/Akt/GSK3beta pathway. Am. J. Physiol. Cell Physiol. 2009, 296, C1310–C1320. [Google Scholar] [CrossRef] [Green Version]
  57. Nejak-Bowen, K.; Kikuchi, A.; Monga, S.P. Beta-catenin-NF-kappaB interactions in murine hepatocytes: A complex to die for. Hepatology 2013, 57, 763–774. [Google Scholar] [CrossRef] [Green Version]
  58. Jang, J.; Ha, J.H.; Chung, S.I.; Yoon, Y. Beta-catenin regulates NF-kappaB activity and inflammatory cytokine expression in bronchial epithelial cells treated with lipopolysaccharide. Int. J. Mol. Med. 2014, 34, 632–638. [Google Scholar] [CrossRef]
  59. Schon, S.; Flierman, I.; Ofner, A.; Stahringer, A.; Holdt, L.M.; Kolligs, F.T.; Herbst, A. beta-catenin regulates NF-kappaB activity via TNFRSF19 in colorectal cancer cells. Int. J. Cancer 2014, 135, 1800–1811. [Google Scholar] [CrossRef]
  60. Vines, A.; Cahoon, S.; Goldberg, I.; Saxena, U.; Pillarisetti, S. Novel anti-inflammatory role for glycogen synthase kinase-3beta in the inhibition of tumor necrosis factor-alpha- and interleukin-1beta-induced inflammatory gene expression. J. Biol. Chem. 2006, 281, 16985–16990. [Google Scholar] [CrossRef] [Green Version]
  61. Robinson, K.F.; Narasipura, S.D.; Wallace, J.; Ritz, E.M.; Al-Harthi, L. β-Catenin and TCFs/LEF signaling discordantly regulate IL-6 expression in astrocytes. Cell Commun. Signal. 2020, 18, 93. [Google Scholar] [CrossRef]
  62. Norris, J.G.; Tang, L.P.; Sparacio, S.M.; Benveniste, E.N. Signal transduction pathways mediating astrocyte IL-6 induction by IL-1 beta and tumor necrosis factor-alpha. J. Immunol. 1994, 152, 841–850. [Google Scholar]
  63. Hunt, P.W.; Sinclair, E.; Rodriguez, B.; Shive, C.; Clagett, B.; Funderburg, N.; Robinson, J.; Huang, Y.; Epling, L.; Martin, J.N.; et al. Gut epithelial barrier dysfunction and innate immune activation predict mortality in treated HIV infection. J. Infect. Dis. 2014, 210, 1228–1238. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Kuller, L.H.; Tracy, R.; Belloso, W.; De Wit, S.; Drummond, F.; Lane, H.C.; Ledergerber, B.; Lundgren, J.; Neuhaus, J.; Nixon, D.; et al. Inflammatory and coagulation biomarkers and mortality in patients with HIV infection. PLoS Med. 2008, 5, e203. [Google Scholar] [CrossRef]
  65. Tenorio, A.R.; Zheng, Y.; Bosch, R.J.; Krishnan, S.; Rodriguez, B.; Hunt, P.W.; Plants, J.; Seth, A.; Wilson, C.C.; Deeks, S.G.; et al. Soluble markers of inflammation and coagulation but not T-cell activation predict non-AIDS-defining morbid events during suppressive antiretroviral treatment. J. Infect. Dis. 2014, 210, 1248–1259. [Google Scholar] [CrossRef] [Green Version]
  66. Poli, G.; Bressler, P.; Kinter, A.; Duh, E.; Timmer, W.; Rabson, A.; Justement, S.; Stanley, S.; Fauci, A. Interleukin 6 induces human immunodeficiency virus expression in infected monocytic cells alone and in synergy with tumor necrosis factor-alpha by transcriptional and post-transcriptional mechanisms. J. Exp. Med. 1990, 172, 151–158. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Poli, G.; Fauci, A.S. The effect of cytokines and pharmacologic agents on chronic HIV infection. AIDS Res. Hum. Retrovir. 1992, 8, 191–197. [Google Scholar] [CrossRef]
  68. Lynch, H.E.; Goldberg, G.L.; Chidgey, A.; Van den Brink, M.R.; Boyd, R.; Sempowski, G.D. Thymic involution and immune reconstitution. Trends Immunol. 2009, 30, 366–373. [Google Scholar] [CrossRef] [Green Version]
  69. Airoldi, M.; Bandera, A.; Trabattoni, D.; Tagliabue, B.; Arosio, B.; Soria, A.; Rainone, V.; Lapadula, G.; Annoni, G.; Clerici, M.; et al. Neurocognitive impairment in HIV-infected naive patients with advanced disease: The role of virus and intrathecal immune activation. Clin. Dev. Immunol. 2012, 2012, 467154. [Google Scholar] [CrossRef] [Green Version]
  70. Velazquez-Salinas, L.; Verdugo-Rodriguez, A.; Rodriguez, L.L.; Borca, M.V. The Role of Interleukin 6 During Viral Infections. Front. Microbiol. 2019, 10, 1057. [Google Scholar] [CrossRef] [Green Version]
  71. Laurenzi, M.A.; Siden, A.; Persson, M.A.; Norkrans, G.; Hagberg, L.; Chiodi, F. Cerebrospinal fluid interleukin-6 activity in HIV infection and inflammatory and noninflammatory diseases of the nervous system. Clin. Immunol. Immunopathol. 1990, 57, 233–241. [Google Scholar] [CrossRef]
  72. Shah, A.; Verma, A.S.; Patel, K.H.; Noel, R.; Rivera-Amill, V.; Silverstein, P.S.; Chaudhary, S.; Bhat, H.K.; Stamatatos, L.; Singh, D.P.; et al. HIV-1 gp120 induces expression of IL-6 through a nuclear factor-kappa B-dependent mechanism: Suppression by gp120 specific small interfering RNA. PLoS ONE 2011, 6, e21261. [Google Scholar] [CrossRef] [Green Version]
  73. Liu, X.; Kumar, A. Differential signaling mechanism for HIV-1 Nef-mediated production of IL-6 and IL-8 in human astrocytes. Sci. Rep. 2015, 5, 9867. [Google Scholar] [CrossRef] [Green Version]
Biomedicines 08 00479 g001 550
Figure 1. β-catenin, LEF-1 and NF-κB mRNA levels in IL-1β and TNF-α treated human astrocytes. Astrocytes were treated with the HIV-associated cytokines interleukin (IL)-1β (20 ng/mL, horizontal line pattern) and tumor necrosis factor (TNF)-α (50 ng/mL, vertical line pattern) alone or in combination (graph check pattern). Total RNA was isolated 8 h post-treatment. (A) β-catenin, (B) lymphoid enhancer-binding factor (LEF)-1 and (C) nuclear factor (NF)-κB mRNA levels were determined by real-time (RT-PCR). Data display mRNA fold changes compared to untreated controls. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a normalizing control. Data cumulative data from three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (*** p < 0.001, compared to an untreated control).
Figure 1. β-catenin, LEF-1 and NF-κB mRNA levels in IL-1β and TNF-α treated human astrocytes. Astrocytes were treated with the HIV-associated cytokines interleukin (IL)-1β (20 ng/mL, horizontal line pattern) and tumor necrosis factor (TNF)-α (50 ng/mL, vertical line pattern) alone or in combination (graph check pattern). Total RNA was isolated 8 h post-treatment. (A) β-catenin, (B) lymphoid enhancer-binding factor (LEF)-1 and (C) nuclear factor (NF)-κB mRNA levels were determined by real-time (RT-PCR). Data display mRNA fold changes compared to untreated controls. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a normalizing control. Data cumulative data from three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (*** p < 0.001, compared to an untreated control).
Biomedicines 08 00479 g001
Biomedicines 08 00479 g002 550
Figure 2. The effects of β-catenin knockdown on LEF-1 and NF-κB induction in activated human astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Astrocytes were then treated with the HIV-associated neurocognitive disorders (HAND)-relevant cytokines IL-1β (20 ng/mL, horizontal pattern) and TNF-α (50 ng/mL, vertical pattern), alone or in combination (graph check pattern). Total RNA was isolated 8 h post-treatment. (A) β-catenin, (B) LEF-1 and (C) NF-κB mRNA levels were determined by RT-PCR. Data display mRNA fold changes compared to untreated controls. GAPDH was used as a normalizing control. Data are cumulative from three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (*** p < 0.001 when compared to Mock or siCon within the treatment). Total protein was isolated 24 h post-treatment and (D) probed for β-catenin. β-catenin levels were quantified by densitometry. GAPDH was used as a loading control. Quantification represents cumulative data from three individual astrocyte donors (*** p < 0.001 when the treatment was compared to Mock or siCon).
Figure 2. The effects of β-catenin knockdown on LEF-1 and NF-κB induction in activated human astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Astrocytes were then treated with the HIV-associated neurocognitive disorders (HAND)-relevant cytokines IL-1β (20 ng/mL, horizontal pattern) and TNF-α (50 ng/mL, vertical pattern), alone or in combination (graph check pattern). Total RNA was isolated 8 h post-treatment. (A) β-catenin, (B) LEF-1 and (C) NF-κB mRNA levels were determined by RT-PCR. Data display mRNA fold changes compared to untreated controls. GAPDH was used as a normalizing control. Data are cumulative from three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (*** p < 0.001 when compared to Mock or siCon within the treatment). Total protein was isolated 24 h post-treatment and (D) probed for β-catenin. β-catenin levels were quantified by densitometry. GAPDH was used as a loading control. Quantification represents cumulative data from three individual astrocyte donors (*** p < 0.001 when the treatment was compared to Mock or siCon).
Biomedicines 08 00479 g002
Biomedicines 08 00479 g003 550
Figure 3. Wound healing and cell proliferation following injury in siβ-catenin transfected astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Post recovery astrocyte monolayers were scratched with a sterile 10 μL pipette tip, and migration of (A1–A4) mock, (B1–B4) siCon, and (C1–C4) siβ-cat transfected astrocytes to the wound site was monitored for 48 h. Phase contrast images captured at 8, 24, 36 and 48 h were shown. Data are representative of three individual donors. Quantified wound healing assay data (D) represent an average remaining wound area ± SEM from four individual astrocyte donors at each timepoint. Statistical analyses were performed using one-way ANOVA with Tukey’s post hoc-test for multiple comparisons (* p < 0.05, ** p < 0.01, *** p < 0.001 when the treatments were compared to either Mock or siCon at a given time point). As a measure of astrocyte proliferation and wound healing levels of cyclin D1 were quantified. Total RNA was isolated, and (E) cyclin D1 mRNA levels were determined by RT-PCR. GAPDH was used as a normalizing control. Data display fold changes in mRNA levels compared to Mock transfected cells. (F) In parallel, 48 h post-transfection, astrocytes were incubated with 10 μM bromodeoxyuridine (BrdU) for 24 h. The graph represents average fold change ± SEM in BrdU incorporation compared to Mock as a measure of cellular proliferation. Data are representative of three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (** p < 0.01, *** p < 0.001 when the bars were compared to either Mock or siCon).
Figure 3. Wound healing and cell proliferation following injury in siβ-catenin transfected astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Post recovery astrocyte monolayers were scratched with a sterile 10 μL pipette tip, and migration of (A1–A4) mock, (B1–B4) siCon, and (C1–C4) siβ-cat transfected astrocytes to the wound site was monitored for 48 h. Phase contrast images captured at 8, 24, 36 and 48 h were shown. Data are representative of three individual donors. Quantified wound healing assay data (D) represent an average remaining wound area ± SEM from four individual astrocyte donors at each timepoint. Statistical analyses were performed using one-way ANOVA with Tukey’s post hoc-test for multiple comparisons (* p < 0.05, ** p < 0.01, *** p < 0.001 when the treatments were compared to either Mock or siCon at a given time point). As a measure of astrocyte proliferation and wound healing levels of cyclin D1 were quantified. Total RNA was isolated, and (E) cyclin D1 mRNA levels were determined by RT-PCR. GAPDH was used as a normalizing control. Data display fold changes in mRNA levels compared to Mock transfected cells. (F) In parallel, 48 h post-transfection, astrocytes were incubated with 10 μM bromodeoxyuridine (BrdU) for 24 h. The graph represents average fold change ± SEM in BrdU incorporation compared to Mock as a measure of cellular proliferation. Data are representative of three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (** p < 0.01, *** p < 0.001 when the bars were compared to either Mock or siCon).
Biomedicines 08 00479 g003
Biomedicines 08 00479 g004 550
Figure 4. CXCL8 and CCL2 levels following β-catenin knockdown in IL-1β and TNF-α-activated human astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Transfected astrocytes were treated with the HIV-associated cytokines, IL-1β (20 ng/mL, horizontal pattern) and TNF-α (50 ng/mL, vertical pattern), alone or in combination (graph check pattern). Cell culture supernatants were collected 24 h post treatment. (A) C-X-C motif chemokine ligand 8 (CXCL8) and (B) C-C motif chemokine ligand 2 (CCL2) protein levels were measured by ELISA and normalized to metabolic activity. Data are representative of three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (*** p < 0.001 when the bars were compared to their respective untreated controls).
Figure 4. CXCL8 and CCL2 levels following β-catenin knockdown in IL-1β and TNF-α-activated human astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Transfected astrocytes were treated with the HIV-associated cytokines, IL-1β (20 ng/mL, horizontal pattern) and TNF-α (50 ng/mL, vertical pattern), alone or in combination (graph check pattern). Cell culture supernatants were collected 24 h post treatment. (A) C-X-C motif chemokine ligand 8 (CXCL8) and (B) C-C motif chemokine ligand 2 (CCL2) protein levels were measured by ELISA and normalized to metabolic activity. Data are representative of three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons (*** p < 0.001 when the bars were compared to their respective untreated controls).
Biomedicines 08 00479 g004
Biomedicines 08 00479 g005 550
Figure 5. IL-6 levels following β-catenin knockdown in IL-1β and TNF-α-activated human astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Post recovery astrocytes were treated with the HIV-associated cytokines IL-1β (20 ng/mL, horizontal pattern) and TNF-α (50 ng/mL, vertical pattern), alone or in combination (graph check pattern). Total RNA was isolated 8 h post-treatment. (A) IL-6 mRNA levels were determined by RT-PCR. Data display mRNA fold changes compared to untreated control. GAPDH was used as a normalizing control. Data are representative of three individual astrocyte donors. Cell culture supernatants were collected 24 h post treatment. (B) Protein levels of IL-6 were measured by ELISA and normalized to metabolic activity. Data are representative of three individual astrocyte donors. Human astrocytes were pretreated with a known GSK-3β inhibitor, BIO (500 nM, dark grey bars) or without (Control, white bars) 1 h prior to treatment with IL-1β and TNF-α. Cell culture supernatants were collected 24 h post treatment. (C) Protein levels of IL-6 were measured by ELISA and normalized to metabolic activity. Data are representative of three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons. (*** p < 0.001 when the bars were compared within the respective treatment groups as indicated).
Figure 5. IL-6 levels following β-catenin knockdown in IL-1β and TNF-α-activated human astrocytes. Astrocytes were transfected with either no siRNA (Mock, white bars), non-targeting siRNA (siCon, light grey bars) or siRNA specific for β-catenin (siβ-cat, dark grey bars). Post recovery astrocytes were treated with the HIV-associated cytokines IL-1β (20 ng/mL, horizontal pattern) and TNF-α (50 ng/mL, vertical pattern), alone or in combination (graph check pattern). Total RNA was isolated 8 h post-treatment. (A) IL-6 mRNA levels were determined by RT-PCR. Data display mRNA fold changes compared to untreated control. GAPDH was used as a normalizing control. Data are representative of three individual astrocyte donors. Cell culture supernatants were collected 24 h post treatment. (B) Protein levels of IL-6 were measured by ELISA and normalized to metabolic activity. Data are representative of three individual astrocyte donors. Human astrocytes were pretreated with a known GSK-3β inhibitor, BIO (500 nM, dark grey bars) or without (Control, white bars) 1 h prior to treatment with IL-1β and TNF-α. Cell culture supernatants were collected 24 h post treatment. (C) Protein levels of IL-6 were measured by ELISA and normalized to metabolic activity. Data are representative of three individual astrocyte donors. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons. (*** p < 0.001 when the bars were compared within the respective treatment groups as indicated).
Biomedicines 08 00479 g005
Biomedicines 08 00479 g006 550
Figure 6. IL-1β-associated GSK-3β phosphorylation and nuclear import of β-catenin and NF-κB in BIO-treated human astrocytes. Primary human astrocytes were treated with IL-1β (20 ng/mL) for 0, 5, 15, 30, and 45 min. Total cell lysates were collected and probed for (A) phosphorylated (p)-GSK-3β, total GSK-3β and GAPDH. (B) Densitometry analysis was used to calculate the p-GSK-3β to GSK-3β ratio at each timepoint. GAPDH was used as a loading control. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons. Data represent average fold change ± SEM from four individual astrocyte donors (* p < 0.05, ** p < 0.01, *** p < 0.001). Human astrocytes were treated with 6-bromoindirubin-3′-oxime (BIO) (500 nM, dark grey bars) or without (Control, white bars). Cytosolic and nuclear fractions of cell lysates were collected 24 h post treatment, (C,E) β-catenin and (D,F) NF-κB levels were determined by the WES capillary protein detection system by using specific antibodies. GAPDH and lamin were used as loading controls for cytosol and nuclear fractions, respectively. Data represent average fold change ± SEM from three individual astrocyte donors. Statistical analyses were performed using student’s t-test (* p < 0.05, ** p < 0.01, *** p < 0.001).
Figure 6. IL-1β-associated GSK-3β phosphorylation and nuclear import of β-catenin and NF-κB in BIO-treated human astrocytes. Primary human astrocytes were treated with IL-1β (20 ng/mL) for 0, 5, 15, 30, and 45 min. Total cell lysates were collected and probed for (A) phosphorylated (p)-GSK-3β, total GSK-3β and GAPDH. (B) Densitometry analysis was used to calculate the p-GSK-3β to GSK-3β ratio at each timepoint. GAPDH was used as a loading control. Statistical analyses were performed using one-way ANOVA with Tukey’s post-hoc test for multiple comparisons. Data represent average fold change ± SEM from four individual astrocyte donors (* p < 0.05, ** p < 0.01, *** p < 0.001). Human astrocytes were treated with 6-bromoindirubin-3′-oxime (BIO) (500 nM, dark grey bars) or without (Control, white bars). Cytosolic and nuclear fractions of cell lysates were collected 24 h post treatment, (C,E) β-catenin and (D,F) NF-κB levels were determined by the WES capillary protein detection system by using specific antibodies. GAPDH and lamin were used as loading controls for cytosol and nuclear fractions, respectively. Data represent average fold change ± SEM from three individual astrocyte donors. Statistical analyses were performed using student’s t-test (* p < 0.05, ** p < 0.01, *** p < 0.001).
Biomedicines 08 00479 g006
Biomedicines 08 00479 g007 550
Figure 7. IL-6 network modeling with HIV-associated molecules from HIV+ astrocyte transcriptomes. Network modeling of the molecules from HIV-1 infected astrocyte transcriptome with HIV encephalitis (HIVE) and HIV-associated dementia (HAD) and biological function is generated using Ingenuity Pathway Analysis (IPA) pathway explorer. The generated pathway shows existing interactions between IL-6, β-catenin, and NF-κB during HIVE and HAD. Interactions between proteins are shown by lines, wherein solid lines represent direct interactions, and dotted lines represent indirect interactions. Protein function is indicated by node shape, e.g., enzyme (diamond), cytokine (square), G-protein coupled receptor (rectangle), kinase (triangle), transcription regulator (oval), microRNA (inverted trapezoid) and other (circle). The node color represents the astroglial proteins that are upregulated (red) or downregulated (green) in the R/G-HIV+ human astrocyte transcriptome [47]. Nodes without color represent transcripts/regulators non-RNA effectors like microRNA, antiretrovirals and amino acids. (Abbreviations: CCL2, chemokine ligand 2; CCL8 chemokine ligand 8; CD40, cluster of differentiation 40; CNR2, cannabinoid receptor 2; CTNNB1, β-catenin; GLS, glutaminase; GSK-3B, glycogen synthase kinase 3 beta; HIF1A, hypoxia inducible factor 1 subunit alpha; HLA-DQA1, major histocompatibility complex, class II, DQ alpha1; IL-6, interleukin 6; LIMS1, LIM zinc finger domain containing 1; MTDH, metadherin; MYLK, myosin light chain kinase; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells; POLB, DNA polymerase beta; POLG, DNA polymerase gamma; PTPRC, protein tyrosine phosphatase receptor type C).
Figure 7. IL-6 network modeling with HIV-associated molecules from HIV+ astrocyte transcriptomes. Network modeling of the molecules from HIV-1 infected astrocyte transcriptome with HIV encephalitis (HIVE) and HIV-associated dementia (HAD) and biological function is generated using Ingenuity Pathway Analysis (IPA) pathway explorer. The generated pathway shows existing interactions between IL-6, β-catenin, and NF-κB during HIVE and HAD. Interactions between proteins are shown by lines, wherein solid lines represent direct interactions, and dotted lines represent indirect interactions. Protein function is indicated by node shape, e.g., enzyme (diamond), cytokine (square), G-protein coupled receptor (rectangle), kinase (triangle), transcription regulator (oval), microRNA (inverted trapezoid) and other (circle). The node color represents the astroglial proteins that are upregulated (red) or downregulated (green) in the R/G-HIV+ human astrocyte transcriptome [47]. Nodes without color represent transcripts/regulators non-RNA effectors like microRNA, antiretrovirals and amino acids. (Abbreviations: CCL2, chemokine ligand 2; CCL8 chemokine ligand 8; CD40, cluster of differentiation 40; CNR2, cannabinoid receptor 2; CTNNB1, β-catenin; GLS, glutaminase; GSK-3B, glycogen synthase kinase 3 beta; HIF1A, hypoxia inducible factor 1 subunit alpha; HLA-DQA1, major histocompatibility complex, class II, DQ alpha1; IL-6, interleukin 6; LIMS1, LIM zinc finger domain containing 1; MTDH, metadherin; MYLK, myosin light chain kinase; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells; POLB, DNA polymerase beta; POLG, DNA polymerase gamma; PTPRC, protein tyrosine phosphatase receptor type C).
Biomedicines 08 00479 g007
Biomedicines 08 00479 g008 550
Figure 8. Crosstalk between Wnt/β-catenin and NF-κB signaling during HIV-associated inflammation. The HIV-associated inflammatory cytokines IL-1β and TNF-α upregulated both Wnt/β-catenin and NF-κB signaling in human astrocytes. Stabilization of β-catenin significantly improved translocation of both β-catenin and NF-κB into nucleus (black arrows). Simultaneously, it decreased IL-1β-mediated expression of IL-6 in astrocytes (dashed red line). In spite of the regulatory overlap between Wnt/β-catenin and NF-κB signaling during HIV-associated inflammation, the mechanism (red dashed arrows) of interaction between these two pathways is yet to be decoded in human astrocytes. IL, interleukin; TNF, tumor necrosis factor; R, receptor; GSK, glycogen synthase kinase; NF-κB, nuclear factor of kappa light polypeptide gene enhancer in B-cells; IκB, NF-κB inhibitor; TCF/LEF, T-cell factor/lymphoid enhancer-binding factor. Created with BioRender.com.
Figure 8. Crosstalk between Wnt/β-catenin and NF-κB signaling during HIV-associated inflammation. The HIV-associated inflammatory cytokines IL-1β and TNF-α upregulated both Wnt/β-catenin and NF-κB signaling in human astrocytes. Stabilization of β-catenin significantly improved translocation of both β-catenin and NF-κB into nucleus (black arrows). Simultaneously, it decreased IL-1β-mediated expression of IL-6 in astrocytes (dashed red line). In spite of the regulatory overlap between Wnt/β-catenin and NF-κB signaling during HIV-associated inflammation, the mechanism (red dashed arrows) of interaction between these two pathways is yet to be decoded in human astrocytes. IL, interleukin; TNF, tumor necrosis factor; R, receptor; GSK, glycogen synthase kinase; NF-κB, nuclear factor of kappa light polypeptide gene enhancer in B-cells; IκB, NF-κB inhibitor; TCF/LEF, T-cell factor/lymphoid enhancer-binding factor. Created with BioRender.com.
Biomedicines 08 00479 g008
Table
Table 1. Gene expression assay target.
Table 1. Gene expression assay target.
TargetAssay Number
(Thermo Fisher)		Dye
Glyceraldehyde 3-phosphate dehydrogenase (GAPDH)4310884E(VIC/TAMRA)
β-cateninHs00355049_m1(FAM/MGB)
Lymphoid enhancement-binding factor (LEF-1)Hs01547250_m1(FAM/MGB)
Interluekin-6 (IL-6)Hs00985639_m1(FAM/MGB)
C-C motif chemokine ligand 2 (CCL2)Hs002341140_m1(FAM/MGB)
C-X-C motif chemokine ligand 8 (CXCL8)Hs00174103_m1(FAM/MGB)
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Edara, V.V.; Nooka, S.; Proulx, J.; Stacy, S.; Ghorpade, A.; Borgmann, K. β-Catenin Regulates Wound Healing and IL-6 Expression in Activated Human Astrocytes. Biomedicines 2020, 8, 479. https://0-doi-org.brum.beds.ac.uk/10.3390/biomedicines8110479

AMA Style

Edara VV, Nooka S, Proulx J, Stacy S, Ghorpade A, Borgmann K. β-Catenin Regulates Wound Healing and IL-6 Expression in Activated Human Astrocytes. Biomedicines. 2020; 8(11):479. https://0-doi-org.brum.beds.ac.uk/10.3390/biomedicines8110479

Chicago/Turabian Style

Edara, Venkata Viswanadh, Shruthi Nooka, Jessica Proulx, Satomi Stacy, Anuja Ghorpade, and Kathleen Borgmann. 2020. "β-Catenin Regulates Wound Healing and IL-6 Expression in Activated Human Astrocytes" Biomedicines 8, no. 11: 479. https://0-doi-org.brum.beds.ac.uk/10.3390/biomedicines8110479

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop