Abstract

Diminished adult neurogenesis is considered a potential mechanism in the pathogenesis of HIV-1-associated dementia (HAD). In HAD, HIV-1-infected and immune-activated brain mononuclear phagocytes (MP; perivascular macrophages and microglia) drive central nervous system (CNS) inflammation and may alter normal neurogenesis. We previously demonstrated HIV-1-infected and lipopolysaccharide (LPS) activated monocyte-derived macrophages (MDM) inhibit human neural progenitor cell (NPC) neurogenesis, while enhancing astrogliogenesis through the secretion of the inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), in vitro and in vivo. Here we further test the hypothesis that HIV-1-infected/activated MDM promote NPC astrogliogenesis via activation of the transcription factor signal transducer and activator of transcription 3 (STAT3), a critical factor for astrogliogenesis. Our results show that LPS-activated MDM-conditioned medium (LPS-MCM) and HIV-infected/LPS-activated MDM-conditioned medium (LPS+HIV-MCM) induced Janus kinase 1 (Jak1) and STAT3 activation. Induction of the Jak-STAT3 activation correlated with increased glia fibrillary acidic protein (GFAP) expression, demonstrating an induction of astrogliogenesis. Moreover, STAT3-targeting siRNA (siSTAT3) decreased MCM-induced STAT3 activation and NPC astrogliogenesis. Furthermore, inflammatory cytokines (including IL-6, IL-1β and TNF-α) produced by LPS-activated and/or HIV-1-infected MDM may contribute to MCM-induced STAT3 activation and astrocytic differentiation. These observations were confirmed in severe combined immunodeficient (SCID) mice with HIV-1 encephalitis (HIVE). In HIVE mice, siRNA control (without target sequence, sicon) pre-transfected NPCs injected with HIV-1-infected MDM showed more astrocytic differentiation and less neuronal differentiation of NPCs as compared to NPC injection alone. siSTAT3 abrogated HIV-1-infected MDM-induced astrogliogenesis of injected NPCs. Collectively, these observations demonstrate that HIV-1-infected/activated MDM induces NPC astrogliogenesis through the STAT3 pathway. This study generates important data elucidating the role of brain inflammation in neurogenesis and may provide insight into new therapeutic strategies for HAD.

Highlights

  • Active neurogenesis occurs throughout life and relies upon the proliferation, migration, and proper differentiation of neural stem/ progenitor cells (NPCs) [1,2]

  • In this study we have further investigated if astrogliogenesis induced by secretion factors from HIV-1-infected MDM (HIV)-1-infected and immune-activated monocyte-derived macrophages (MDM) is through the signal transducer and activator of transcription 3 (STAT3) pathway

  • To extend on our previous findings, we examined the function of the Jak-STAT3 pathway, a crucial part of the astrogliogenic machinery, in HIV-1infected and/or immune-activated MDM conditioned medium (MCM)-induced NPC differentiation

Read more

Summary

Introduction

Active neurogenesis occurs throughout life and relies upon the proliferation, migration, and proper differentiation of neural stem/ progenitor cells (NPCs) [1,2]. During HAD, HIV-1-infected and immune-activated brain mononuclear phagocytes (MP; perivascular macrophages and microglia) release many immune competent factors including cytokines, viral proteins and neurotoxins. These factors are involved in neuronal injury, drive central nervous system (CNS) inflammation, and may alter normal neurogenesis [14,15,16,17, 18,19]. Our previous work demonstrated HIV-1-infected and immune-activated monocyte-derived macrophages (MDM) inhibit neurogenesis, while enhancing astrogliogenesis through secretion of inflammatory cytokines such as IL-1b and TNF-a [9]. The signaling pathways involved in this process are unknown

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.