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原发性外周血单个核细胞感染人类免疫缺陷病毒(HIV-1)中 miRNA 和 mRNA 的比较表达谱。

Comparative expression profile of miRNA and mRNA in primary peripheral blood mononuclear cells infected with human immunodeficiency virus (HIV-1).

机构信息

Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.

出版信息

PLoS One. 2011;6(7):e22730. doi: 10.1371/journal.pone.0022730. Epub 2011 Jul 28.

Abstract

Host cells respond to exogenous infectious agents such as viruses, including HIV-1. Studies have evaluated the changes associated with virus infection at the transcriptional and translational levels of the cellular genes involved in specific pathways. While this approach is useful, in our view it provides only a partial view of genome-wide changes. Recently, technological advances in the expression profiling at the microRNA (miRNA) and mRNA levels have made it possible to evaluate the changes in the components of multiple pathways. To understand the role of miRNA and its interplay with host cellular gene expression (mRNA) during HIV-1 infection, we performed a comparative global miRNA and mRNA microarray using human PBMCs infected with HIV-1. The PBMCs were derived from multiple donors and were infected with virus generated from the molecular clone pNL4-3. The results showed that HIV-1 infection led to altered regulation of 21 miRNAs and 444 mRNA more than 2-fold, with a statistical significance of p<0.05. Furthermore, the differentially regulated miRNA and mRNA were shown to be associated with host cellular pathways involved in cell cycle/proliferation, apoptosis, T-cell signaling, and immune activation. We also observed a number of inverse correlations of miRNA and mRNA expression in infected PBMCs, further confirming the interrelationship between miRNA and mRNA regulation during HIV-1 infection. These results for the first time provide evidence that the miRNA profile could be an early indicator of host cellular dysfunction induced by HIV-1.

摘要

宿主细胞对外源感染因子(如病毒,包括 HIV-1)产生应答。研究评估了病毒感染相关的基因在特定途径中的转录和翻译水平的变化。虽然这种方法很有用,但在我们看来,它只提供了基因组范围内变化的部分视图。最近,在 microRNA(miRNA)和 mRNA 水平的表达谱技术的进步使得评估多个途径组成部分的变化成为可能。为了了解 miRNA 的作用及其与 HIV-1 感染过程中宿主细胞基因表达(mRNA)的相互作用,我们使用感染了 HIV-1 的人 PBMC 进行了比较全局 miRNA 和 mRNA 微阵列分析。PBMC 来自多个供体,并感染了来自分子克隆 pNL4-3 的病毒。结果表明,HIV-1 感染导致 21 个 miRNA 和 444 个 mRNA 的调节发生改变,倍数变化超过 2 倍,p 值<0.05。此外,差异调节的 miRNA 和 mRNA 与涉及细胞周期/增殖、凋亡、T 细胞信号转导和免疫激活的宿主细胞途径相关。我们还观察到感染的 PBMC 中 miRNA 和 mRNA 表达的许多反向相关性,进一步证实了 HIV-1 感染过程中 miRNA 和 mRNA 调节之间的相互关系。这些结果首次提供了证据,表明 miRNA 谱可能是 HIV-1 诱导的宿主细胞功能障碍的早期指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a631/3145673/e506d12fc5f9/pone.0022730.g001.jpg

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