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Up-regulation of microRNA-142 in simian immunodeficiency virus encephalitis leads to repression of sirtuin1

机译:猿猴免疫缺陷病毒脑炎中microRNA-142的上调导致sirtuin1的抑制

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摘要

MicroRNA (miR)-142 is up-regulated in the brain in HIV and SIV encephalitis (SIVE). We identified the cell types where miR-142 is up-regulated and its relevant downstream target. Fluorescent in situ hybridization combined with immunofluorescent labeling revealed that miR-142-3p and -5p are expressed within hippocampal neurons and myeloid cells in SIVE. Sirtuin1 (SIRT1) was predicted as a potential miR-142 target by analysis of its 3′-UTR and bioinformatic analysis of factors linked to altered hippocampal gene expression profile in SIVE. Overexpression of pre-miR-142 in HEK293T cells led to a 3.7-fold decrease in SIRT1 protein level. Examination of the individual effects of miR-142-5p and miR-142-3p through overexpression and inhibition studies revealed that significant effects on SIRT1 occurred only with miR-142-5p. Luciferase reporter assays revealed a 2.3-fold inhibition of expression due to interaction of miR-142 with the SIRT1 3′-UTR, mutation analysis revealed that only the miR-142-5p target site was active. MiR-142 expression in primary human neurons led to a small (1.3-fold) but significant decrease in SIRT1 protein level. Furthermore, qRT-PCR revealed up-regulation of miR-142-3p (6.4-fold) and -5p (3.9-fold) and down-regulation of SIRT1 (33-fold) in macrophages/microglia from animals with SIVE. We have therefore elucidated a miR-mediated mechanism of regulation of SIRT1 expression in SIVE.—Chaudhuri, A. D., Yelamanchili, S. V., Marcondes, M. C. G., Fox, H. S. Up-regulation of microRNA-142 in simian immunodeficiency virus encephalitis leads to repression of sirtuin1.
机译:在HIV和SIV脑炎(SIVE)中,大脑中的MicroRNA(miR)-142上调。我们确定了miR-142上调的细胞类型及其相关的下游靶标。荧光原位杂交结合免疫荧光标记显示,miR-142-3p和-5p在SIVE的海马神经元和髓样细胞内表达。通过对Sirtuin1(SIRT1)的3'-UTR的分析和与SIVE中海马基因表达谱改变有关的因素的生物信息学分析,预测其可能是miR-142的潜在靶标。 premiR-142在HEK293T细胞中的过度表达导致SIRT1蛋白水平降低了3.7倍。通过过度表达和抑制研究检查了miR-142-5p和miR-142-3p的个体作用,结果表明,仅对miR-142-5p发生了对SIRT1的显着影响。萤光素酶报告基因检测显示,由于miR-142与SIRT1 3'-UTR的相互作用,其表达受到了2.3倍的抑制。突变分析表明,只有miR-142-5p靶位具有活性。原人类神经元中的MiR-142表达导致SIRT1蛋白水平小(1.3倍)但显着下降。此外,qRT-PCR揭示了SIVE动物巨噬细胞/小胶质细胞中miR-142-3p(6.4倍)和-5p(3.9倍)的上调以及SIRT1(33倍)的下调。因此,我们阐明了miR介导的SIVE中SIRT1表达调控的机制。-Chaudhuri,AD,Yelamanchili,SV,Marcondes,MCG,Fox,HS在猿猴免疫缺陷病毒性脑炎中microRNA-142的上调导致sirtuin1的抑制。 。

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