The Epigenetic Role of miR-124 in HIV-1 Tat- and Cocaine-Mediated Microglial Activation

Int J Mol Sci. 2022 Nov 30;23(23):15017. doi: 10.3390/ijms232315017.

Abstract

HIV-1 and drug abuse have been indissolubly allied as entwined epidemics. It is well-known that drug abuse can hasten the progression of HIV-1 and its consequences, especially in the brain, causing neuroinflammation. This study reports the combined effects of HIV-1 Transactivator of Transcription (Tat) protein and cocaine on miR-124 promoter DNA methylation and its role in microglial activation and neuroinflammation. The exposure of mouse primary microglial cells to HIV-1 Tat (25 ng/mL) and/or cocaine (10 μM) resulted in the significantly decreased expression of primary (pri)-miR-124-1, pri-miR-124-2, and mature miR-124 with a concomitant upregulation in DNMT1 expression as well as global DNA methylation. Our bisulfite-converted genomic DNA sequencing also revealed significant promoter DNA methylation in the pri-miR-124-1 and pri-miR-124-2 in HIV-1 Tat- and cocaine-exposed mouse primary microglial cells. We also found the increased expression of proinflammatory cytokines such as IL1β, IL6 and TNF in the mouse primary microglia exposed to HIV-1 Tat and cocaine correlated with microglial activation. Overall, our findings demonstrate that the exposure of mouse primary microglia to both HIV-1 Tat and cocaine could result in intensified microglial activation via the promoter DNA hypermethylation of miR-124, leading to the exacerbated release of proinflammatory cytokines, ultimately culminating in neuroinflammation.

Keywords: DNA methylation; HIV-1 Tat; HIV-1 associated neurocognitive disorders; cocaine; epigenetics; microglia; neuroinflammation.

MeSH terms

  • Animals
  • Cells, Cultured
  • Cocaine* / metabolism
  • Cocaine* / pharmacology
  • Cytokines / metabolism
  • HIV-1* / genetics
  • HIV-1* / metabolism
  • Mice
  • MicroRNAs* / metabolism
  • Microglia / metabolism
  • Trans-Activators / metabolism
  • tat Gene Products, Human Immunodeficiency Virus / metabolism

Substances

  • Cocaine
  • Trans-Activators
  • MicroRNAs
  • tat Gene Products, Human Immunodeficiency Virus
  • Cytokines
  • Mirn124 microRNA, mouse