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miR-628是一种由Toll样受体刺激诱导产生的微小RNA,它可调节猪的先天免疫反应。

miR-628, a microRNA that is induced by Toll-like receptor stimulation, regulates porcine innate immune responses.

作者信息

Jun He, Ying He, Daiwen Chen, Bing Yu, Xiangbing Mao, Ping Zheng, Jie Yu, Zhiqing Huang, Junqiu Luo

机构信息

1] Institute of Animal Nutrition, Sichuan Agricultural University, Ya'an, Sichuan 625014, P. R. China [2] Key Laborotary of Animal Disease-Resistance Nutrition, Ministry of Education, China.

出版信息

Sci Rep. 2015 Jul 31;5:12226. doi: 10.1038/srep12226.

Abstract

Mammalian innate and acquired immune responses involve a coordinated, sequential, and self limiting sequence of events controlled by positive and negative regulatory mechanism. MicroRNAs have been implicated as a negative regulator for diverse biological events including immune responses. However, the involvement of miRNAs in regulating the immune responses is just beginning to be explored. Here, we characterized the expression profiling of 375 microRNAs in porcine monocytes induced by lipopolysaccharide (LPS), and result shows that several of them are endotoxin-responsive genes. Through promoter analysis, the miR-628 was found to be a NF-κB dependent gene. Importantly, miR-628 was predicted to base-pair with sequences in the 3'-UTR of the myeloid differentiation protein 88 (MyD88) gene. And we found that the UTR inhibit expression of a linked reporter gene coding a key adapter molecule downstream of Toll-like receptors (TLRs), resulting in suppressing of the TLR signaling. Therefore, we not only propose a role of miR-628 in control of the TLR signaling through a negative feedback regulation loop involving down-regulation of MyD88 protein levels, but results may also contribute to rational target selection orchestrating the inflammatory responses.

摘要

哺乳动物的先天性和获得性免疫反应涉及由正负调节机制控制的一系列协调、有序且自我限制的事件。微小RNA(miRNA)已被认为是包括免疫反应在内的多种生物学事件的负调节因子。然而,miRNA在调节免疫反应中的作用才刚刚开始被探索。在此,我们对脂多糖(LPS)诱导的猪单核细胞中375种微小RNA的表达谱进行了表征,结果表明其中几种是内毒素反应基因。通过启动子分析,发现miR-628是一种依赖NF-κB的基因。重要的是,预测miR-628与髓样分化蛋白88(MyD88)基因3'-UTR中的序列形成碱基对。并且我们发现该UTR抑制编码Toll样受体(TLR)下游关键衔接分子的报告基因的表达,从而导致TLR信号传导受到抑制。因此,我们不仅提出了miR-628通过涉及下调MyD88蛋白水平的负反馈调节环在控制TLR信号传导中的作用,而且这些结果可能也有助于合理选择调节炎症反应的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e0/4521185/c28a6678768a/srep12226-f1.jpg

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