Proteomics reveals different pathological processes of adipose tissue, liver, and skeletal muscle under insulin resistance

被引:6
作者
Li, Yaqi [1 ]
Ma, Quantao [1 ]
Li, Pengfei [1 ]
Wang, Jingkang [1 ]
Wang, Min [1 ]
Fan, Yuanyuan [1 ]
Wang, Tieshan [2 ]
Wang, Chunguo [2 ]
Wang, Ting [2 ]
Zhao, Baosheng [2 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing, Peoples R China
[2] Beijing Univ Chinese Med, Beijing Res Inst Chinese Med, 11 North 3rd Ring East Rd, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
adipose tissue; diabetes mellitus Type 2; insulin resistance; liver; muscle; proteomics; skeletal; LONG NONCODING RNAS; RENIN-ANGIOTENSIN-SYSTEM; FOAM CELL-FORMATION; CHAIN AMINO-ACIDS; BINDING PROTEIN; MOUSE MODEL; EXTRACELLULAR-MATRIX; GLUCOSE-INTOLERANCE; DIABETIC-PATIENTS; LIPID-METABOLISM;
D O I
10.1002/jcp.29658
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Type 2 diabetes mellitus is the most common type of diabetes, and insulin resistance (IR) is its core pathological mechanism. Proteomics is an ingenious and promising Omics technology that can comprehensively describe the global protein expression profiling of body or specific tissue, and is widely applied to the study of molecular mechanisms of diseases. In this paper, we focused on insulin target organs: adipose tissue, liver, and skeletal muscle, and analyzed the different pathological processes of IR in these three tissues based on proteomics research. By literature studies, we proposed that the main pathological processes of IR among target organs were diverse, which showed unique characteristics and focuses. We further summarized the differential proteins in target organs which were verified to be related to IR, and discussed the proteins that may play key roles in the emphasized pathological processes, aiming at discovering potentially specific differential proteins of IR, and providing new ideas for pathological mechanism research of IR.
引用
收藏
页码:6441 / 6461
页数:21
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