Literature DB >> 27888215

Super-resolution microscopy reveals the insulin-resistance-regulated reorganization of GLUT4 on plasma membranes.

Lan Gao1,2, Junling Chen2,3, Jing Gao2,3, Hongda Wang4, Wenyong Xiong5.   

Abstract

GLUT4 (also known as SLC2A4) is essential for glucose uptake in skeletal muscles and adipocytes, which play central roles in whole-body glucose metabolism. Here, using direct stochastic optical reconstruction microscopy (dSTORM) to investigate the characteristics of plasma-membrane-fused GLUT4 at the single-molecule level, we have demonstrated that insulin and insulin resistance regulate the spatial organization of GLUT4 in adipocytes. Stimulation with insulin shifted the balance of GLUT4 on the plasma membrane toward a more dispersed configuration. In contrast, insulin resistance induced a more clustered distribution of GLUT4 and increased the mean number of molecules per cluster. Furthermore, our data demonstrate that the F5QQI motif and lipid rafts mediate the maintenance of GLUT4 clusters on the plasma membrane. Mutation of F5QQI (F5QQA-GLUT4) induced a more clustered distribution of GLUT4; moreover, destruction of lipid rafts in adipocytes expressing F5QQA-GLUT4 dramatically decreased the percentage of large clusters and the mean number of molecules per cluster. In conclusion, our data clarify the effects of insulin stimulation or insulin resistance on GLUT4 reorganization on the plasma membrane and reveal new pathogenic mechanisms of insulin resistance.
© 2017. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Direct stochastic optical reconstruction microscopy; GLUT4; Insulin resistance; Membrane protein; dSTORM

Mesh:

Substances:

Year:  2016        PMID: 27888215     DOI: 10.1242/jcs.192450

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  12 in total

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8.  Fluorescence Microscopy-Based Quantitation of GLUT4 Translocation: High Throughput or High Content?

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9.  Aging-associated changes in CD47 arrangement and interaction with thrombospondin-1 on red blood cells visualized by super-resolution imaging.

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10.  Super-Resolution Live Cell Microscopy of Membrane-Proximal Fluorophores.

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