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miR-608 通过靶向单核细胞中的 ELANE 发挥抗炎作用。

MiR-608 Exerts Anti-inflammatory Effects by Targeting ELANE in Monocytes.

机构信息

School of Medicine, Changing University, Shapingba, Chongqing, 400045, China.

Key Laboratory of Biorheological Science and Technology (Chongqing University), Ministry of Education, School of Medicine, Chongqing University, Shapingba, Chongqing, 400045, China.

出版信息

J Clin Immunol. 2020 Jan;40(1):147-157. doi: 10.1007/s10875-019-00702-8. Epub 2019 Nov 20.

Abstract

miR-608 has been indicated to play an important role in the pathogenesis of various inflammation-related diseases, including sepsis and several types of cancers. However, there is little information about the underlying mechanism, especially in inflammatory cells. In this study, an hsa-miR-608-inhibition cell model was constructed in U937 cells using a lentivirus, and gene expression profiles were determined by a cDNA microarray. Altogether, 682 genes showed a difference greater than 1.2-fold, including 184 genes downregulated and 498 genes upregulated. Among these genes, one potential miR-608-target gene, ELANE, was further investigated. A positive relationship between the expression of miR-608 and that of ELANE was found both in vivo and in vitro. In addition, decreased expression of miR-608 resulted in overexpression of ELANE at both the mRNA and protein levels. Cotransfection of HEK293T cells with a miR-608 mimic inhibited reporter activity, and mutation of the miRNA seed sequences abolished the repression of reporter activity. These results suggest that miR-608 is an important posttranscriptional regulator of ELANE expression in human monocytes and may play an important role in the process of inflammation. miR-608 and neutrophil elastase may be novel targets for the diagnosis or treatment of sepsis.

摘要

miR-608 在各种炎症相关疾病(包括脓毒症和几种类型的癌症)的发病机制中发挥着重要作用。然而,关于其潜在机制的信息很少,特别是在炎症细胞中。在这项研究中,使用慢病毒构建了 U937 细胞中的 hsa-miR-608 抑制细胞模型,并通过 cDNA 微阵列确定了基因表达谱。总共有 682 个基因的差异大于 1.2 倍,包括 184 个下调基因和 498 个上调基因。在这些基因中,进一步研究了一个潜在的 miR-608 靶基因,ELANE。在体内和体外都发现 miR-608 的表达与 ELANE 的表达呈正相关。此外,miR-608 表达的降低导致 ELANE 在 mRNA 和蛋白水平上的过表达。HEK293T 细胞共转染 miR-608 模拟物抑制报告基因活性,而 miRNA 种子序列的突变则消除了对报告基因活性的抑制。这些结果表明,miR-608 是人类单核细胞中 ELANE 表达的重要转录后调节因子,可能在炎症过程中发挥重要作用。miR-608 和中性粒细胞弹性蛋白酶可能是脓毒症诊断或治疗的新靶点。

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