Mechanism of INSR clustering with insulin activation and resistance revealed by super-resolution imaging.
Hongru LiJinrui ZhangYan ShiGuanfang ZhaoHaijiao XuMingjun CaiHongda WangQiuyan YanPublished in: Nanoscale (2022)
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 βII-spectrin. Specific knockout of βII-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.
Keyphrases
- insulin resistance
- type diabetes
- single molecule
- glycemic control
- adipose tissue
- high fat diet
- metabolic syndrome
- signaling pathway
- high resolution
- skeletal muscle
- single cell
- atomic force microscopy
- epithelial mesenchymal transition
- binding protein
- blood glucose
- immune response
- rna seq
- regulatory t cells
- climate change
- dendritic cells
- cell proliferation
- small molecule
- induced apoptosis
- protein protein