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在肝脏中抑制胰岛素受体底物-1(IRS-1)表达的微小RNA的鉴定。

Identification of microRNA that represses IRS-1 expression in liver.

作者信息

Ono Kaoru, Igata Motoyuki, Kondo Tatsuya, Kitano Sayaka, Takaki Yuki, Hanatani Satoko, Sakaguchi Masaji, Goto Rieko, Senokuchi Takafumi, Kawashima Junji, Furukawa Noboru, Motoshima Hiroyuki, Araki Eiichi

机构信息

Department of Metabolic Medicine, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.

出版信息

PLoS One. 2018 Jan 24;13(1):e0191553. doi: 10.1371/journal.pone.0191553. eCollection 2018.

Abstract

MicroRNAs (miRNAs) are short, non-coding RNAs that post-transcriptionally regulate gene expression and have been shown to participate in almost every cellular process. Several miRNAs have recently been implicated in glucose metabolism, but the roles of miRNAs in insulin-resistant conditions, such as obesity or type 2 diabetes, are largely unknown. Herein, we focused on miR-222, the expression of which was increased in the livers of high fat/high sucrose diet-fed mice injected with gold thioglucose (G+HFHSD). Overexpression of miR-222 in primary mouse hepatocytes attenuated Akt phosphorylation induced by insulin, indicating that miR-222 negatively regulates insulin signaling. As per in silico analysis, miR-222 potentially binds to the 3' untranslated region (3' UTR) of the IRS-1 gene, a key insulin signaling molecule. In fact, IRS-1 protein expression was decreased in the livers of G+HFHSD-fed mice. We further confirmed a direct interaction between miR-222 and the 3' UTR of IRS-1 via luciferase assays. Our findings suggest that up-regulation of miR-222 followed by reduction in IRS-1 expression may be a viable mechanism of insulin resistance in the liver.

摘要

微小RNA(miRNA)是短链非编码RNA,可在转录后调节基因表达,并已被证明参与几乎所有细胞过程。最近有几种miRNA与葡萄糖代谢有关,但miRNA在肥胖或2型糖尿病等胰岛素抵抗状态中的作用尚不清楚。在此,我们聚焦于miR-222,在用硫代葡萄糖金注射的高脂/高蔗糖饮食喂养小鼠(G+HFHSD)的肝脏中,其表达增加。在原代小鼠肝细胞中过表达miR-222可减弱胰岛素诱导的Akt磷酸化,表明miR-222负向调节胰岛素信号传导。根据计算机分析,miR-222可能与关键胰岛素信号分子IRS-1基因的3'非翻译区(3'UTR)结合。事实上,在G+HFHSD喂养小鼠的肝脏中,IRS-1蛋白表达降低。我们通过荧光素酶测定进一步证实了miR-222与IRS-1的3'UTR之间存在直接相互作用。我们的研究结果表明,miR-222上调随后IRS-1表达降低可能是肝脏胰岛素抵抗的一种可行机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c49/5783395/a99079907ff6/pone.0191553.g001.jpg

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