HIV-1 Tat and cocaine impact astrocytic energy reservoir influence on miRNA epigenetic regulation

被引:7
作者
Doke, Mayur [1 ]
Kashanchi, Fatah [2 ]
Khan, Mansoor A. [1 ]
Samikkannu, Thangavel [1 ]
机构
[1] Texas A&M Univ, Irma Lerma Rangel Coll Pharm, Dept Pharmaceut Sci, 1010 W Ave B, Kingsville, TX 78363 USA
[2] George Mason Univ, Natl Ctr Biodef & Infect Dis, Lab Mol Virol, Manassas, VA 20110 USA
关键词
miRNA; HIV-1; Tat; Piracetam; Astrocyte and cocaine; R/BIOCONDUCTOR PACKAGE; CELL-PROLIFERATION; MICRORNA GENES; EXPRESSION; DISEASE; MECHANISMS; SCHIZOPHRENIA; CYTOKINES; RECEPTOR; DRUGS;
D O I
10.1016/j.ygeno.2021.08.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Astrocytes are the primary regulator of energy metabolism in the central nervous system (CNS), and impairment of astrocyte's energy resource may trigger neurodegeneration. HIV infections and cocaine use are known to alter epigenetic modification, including miRNAs, which can target gene expression post-transcriptionally. However, miRNA-mediated astrocyte energy metabolism has not been delineated in HIV infection and cocaine abuse. Using next-generation sequencing (NGS), we identified a total of 1900 miRNAs, 64 were upregulated and 68 miRNAs were downregulated in the astrocytes by HIV-1 Tat with cocaine exposure. Moreover, miR-4727-3p, miR-51895p, miR-5090, and miR-6810-5p expressions were significantly impacted, and their gene targets were identified as VAMP2, NFIB, PPM1H, MEIS1, and PSD93 through the bioinformatic approach. In addition, the astrocytes treated with the nootropic drug piracetam protects these miRNAs. These findings provide evidence that the miRNAs in the astrocytes may be a potential biomarker and therapeutic target for HIV and cocaine abuseinduced neurodegeneration.
引用
收藏
页码:3461 / 3475
页数:15
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