Gonadal white adipose tissue-derived exosomal MiR-222 promotes obesity-associated insulin resistance

被引:6
作者
Song, Huichen [1 ]
Li, Dameng [1 ]
Shuo, Linghu [1 ]
Wang, Lei [1 ]
Xie, Ping [1 ]
Li, Weili [1 ]
Liu, Jiachen [1 ]
Tong, Yafei [1 ]
Zhang, Chen-Yu [1 ]
Jiang, Xiaohong [1 ]
Li, Jing [1 ]
Zhang, Yujing [1 ]
机构
[1] Nanjing Univ, Nanjing DrumTower Hosp, Ctr Mol Diagnost & Therapy,Sch Life Sci,NJU Inst, State Key Lab Pharmaceut Biotechnol,Jiangsu Engn, Nanjing 210023, Peoples R China
来源
AGING-US | 2020年 / 12卷 / 22期
基金
中国国家自然科学基金;
关键词
miR-222; adipose; insulin resistance; liver; skeletal muscle; CIRCULATING MICRORNAS; TNF-ALPHA; CANCER; BIOGENESIS; EXPRESSION; MIRNAS; CELLS; LINK; FAT;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In this study, we investigated the role of serum exosomal miR-222 in obesity-related insulin resistance. Bioinformatics analyses showed that miR-222 levels were significantly upregulated in the white adipose tissue of obese patients with insulin resistance (GSE25402 dataset) and in serum samples from type 2 diabetes mellitus (T2DM) patients (GSE90028 dataset). Moreover, analysis of miRNA expression in adipose tissue specific Dicer knockout mice (GitHub dataset) and diabetic model mice (GSE81976 and GSE85101 datasets), gonadal white adipose tissue (gWAT) was the main source of serum exosomal miR-222. MiR-222 levels were significantly elevated in the serum, serum exosomes and gWAT of mice fed a high-fat diet (HFD), and there was a corresponding downregulation of IRS1 and phospho-AKT levels in their liver and skeletal muscle tissues, which correlated with impaired insulin sensitivity and glucose intolerance. These effects were abrogated by surgically removing the gWAT from the HFD-fed mice. Thus, gWAT-derived serum exosomal miR-222 appears to promote insulin resistance in the liver and skeletal muscle of HFD-fed obese mice by suppressing IRS1 expression.
引用
收藏
页码:22719 / 22743
页数:25
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