Mechanism of INSR clustering with insulin activation and resistance revealed by super-resolution imaging

被引:7
|
作者
Li, Hongru [1 ,2 ]
Zhang, Jinrui [1 ]
Shi, Yan [1 ]
Zhao, Guanfang [1 ,2 ]
Xu, Haijiao [1 ]
Cai, Mingjun [1 ,2 ]
Gao, Jing [1 ]
Wang, Hongda [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China
[3] Qing Dao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Wenhai Rd, Qingdao 266237, Shandong, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
RECEPTOR; MICROSCOPY; SPECTRIN; GLUT4; PROTEINS; SKELETON; DOMAIN;
D O I
10.1039/d2nr01051h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Insulin receptor (INSR) is a key protein in the INSR signaling pathway and plays a critical role in biological processes, especially in the regulation of glucose homeostasis. Many metabolic diseases are often accompanied by abnormal INSR signaling. However, the specific effector mechanisms regulating insulin resistance and the distribution patterns of INSR during cell membrane activation remain unclear. Here, we investigated the changes in the distribution of INSR during activation using super-resolution imaging. By observing the connection between INSR activation and its distribution, we found that insulin resistance inhibits its receptor clustering. More importantly, we found that INSR has a highly co-localized relationship with the skeletal protein beta II-spectrin. Specific knockout of beta II-spectrin inhibited the interaction of INSR with GLUT4 and affected the normal metabolism of glucose. Our work elucidates the effects of insulin activation and insulin resistance on INSR distribution and reveals a potential relationship between INSR and cytoskeleton at the single molecule level, which promotes a deeper understanding of the roles associated with insulin signaling and insulin resistance.
引用
收藏
页码:7747 / 7755
页数:9
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