Yang Won-Mo, Min Kyung-Ho, Lee Wan
Department of Biochemistry, Dongguk University College of Medicine, Gyeongju, 780-714, South Korea.
Department of Biochemistry, Dongguk University College of Medicine, Gyeongju, 780-714, South Korea; Endocrine Channelopathy, Channelopathy Research Center, Dongguk University College of Medicine, Goyang, 410-773, South Korea.
Biochem Biophys Res Commun. 2016 Sep 30;478(4):1786-91. doi: 10.1016/j.bbrc.2016.09.029. Epub 2016 Sep 7.
Dietary saturated fatty acids (SFA) in excess not only induce hepatic insulin resistance, but also result in type 2 diabetes (T2DM). Although microRNAs (miRNAs) participate widely in the pathogenesis of a range of diseases through the suppression of target gene expression at the post-transcriptional level, the implications of SFA-induced miRNAs in the dysregulation of metabolism, particularly in the development of insulin resistance, are largely unclear. SFA palmitate provoked an impairment of insulin signaling in HepG2 cells via a reduction in the expression of INSR and IRS-1 protein. The significant upregulation of miR-1271, which was presumed to target INSR and IRS-1 3'UTRs, was observed in the palmitate-treated HepG2 cells. Using a reporter gene assay, miR-1271 authentically targeted the 3'UTRs of INSR and IRS-1. Furthermore, the overexpression of miR-1271 caused a substantial decrease in INSR and IRS-1 expression, which led to an impairment in insulin signaling and glycogen metabolism. Therefore, these findings suggest that the induction of miR-1271 by SFA palmitate promotes the development of insulin resistance by targeting INSR and IRS-1 in hepatocytes.
过量的膳食饱和脂肪酸(SFA)不仅会诱发肝脏胰岛素抵抗,还会导致2型糖尿病(T2DM)。尽管微小RNA(miRNA)通过在转录后水平抑制靶基因表达而广泛参与一系列疾病的发病机制,但SFA诱导的miRNA在代谢失调,尤其是胰岛素抵抗发展中的作用在很大程度上尚不清楚。饱和脂肪酸棕榈酸酯通过降低胰岛素受体(INSR)和胰岛素受体底物-1(IRS-1)蛋白的表达,引发HepG2细胞中胰岛素信号传导的损伤。在棕榈酸酯处理的HepG2细胞中观察到miR-1271的显著上调,推测其靶向INSR和IRS-1的3'非翻译区(3'UTR)。使用报告基因测定法,miR-1271确实靶向INSR和IRS-1的3'UTR。此外,miR-1271的过表达导致INSR和IRS-1表达大幅下降,进而导致胰岛素信号传导和糖原代谢受损。因此,这些发现表明,棕榈酸酯饱和脂肪酸诱导的miR-1271通过靶向肝细胞中的INSR和IRS-1促进胰岛素抵抗的发展。