Roles of long noncoding RNAs and small extracellular vesicle-long noncoding RNAs in type 2 diabetes

被引:11
|
作者
Chang, Wenguang [1 ]
Wang, Man [1 ]
Zhang, Yuan [1 ]
Yu, Fei [1 ]
Hu, Bin [2 ]
Goljanek-Whysall, Katarzyna [3 ]
Li, Peifeng [1 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Coll Med, Inst Translat Med, Qingdao, Peoples R China
[2] Univ Aberdeen, Sch Med Med Sci & Nutr, Inst Med Sci IMS, Aberdeen, Scotland
[3] Natl Univ Ireland, Coll Med, Dept Physiol Nursing & Hlth Sci, Galway, Ireland
基金
中国国家自然科学基金;
关键词
diabetes; exosomes; long noncoding RNA; small extracellular vesicle; sorting mechanism; SKELETAL-MUSCLE; MITOCHONDRIAL-FUNCTION; MESSENGER-RNAS; HIGH GLUCOSE; EARLY-STAGE; LNCRNA; EXPRESSION; CELLS; EXOSOMES; MALAT1;
D O I
10.1111/tra.12868
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The prevalence of a high-energy diet and a sedentary lifestyle has increased the incidence of type 2 diabetes (T2D). T2D is a chronic disease characterized by high blood glucose levels and insulin resistance in peripheral tissues. The pathological mechanism of this disease is not fully clear. Accumulated evidence has shown that noncoding RNAs have an essential regulatory role in the progression of diabetes and its complications. The roles of small noncoding RNAs, such as miRNAs, in T2D, have been extensively investigated, while the function of long noncoding RNAs (lncRNAs) in T2D has been unstudied. It has been reported that lncRNAs in T2D play roles in the regulation of pancreatic function, peripheral glucose homeostasis and vascular inflammation. In addition, lncRNAs carried by small extracellular vesicles (sEV) were shown to mediate communication between organs and participate in diabetes progression. Some sEV lncRNAs derived from stem cells are being developed as potential therapeutic agents for diabetic complications. In this review, we summarize the current knowledge relating to lncRNA biogenesis, the mechanisms of lncRNA sorting into sEV and the regulatory roles of lncRNAs and sEV lncRNAs in diabetes. Knowledge of lncRNAs and sEV lncRNAs in diabetes will aid in the development of new therapeutic drugs for T2D in the future.
引用
收藏
页码:526 / 537
页数:12
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