Gao Lan, Chen Junling, Gao Jing, Wang Hongda, Xiong Wenyong
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan 650201, P.R. China.
Graduate University of Chinese Academy of Sciences, Beijing 100049, P.R. China.
J Cell Sci. 2017 Jan 15;130(2):396-405. doi: 10.1242/jcs.192450. Epub 2016 Nov 25.
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 FQQI motif and lipid rafts mediate the maintenance of GLUT4 clusters on the plasma membrane. Mutation of FQQI (FQQA-GLUT4) induced a more clustered distribution of GLUT4; moreover, destruction of lipid rafts in adipocytes expressing FQQA-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.
葡萄糖转运蛋白4(也称为溶质载体家族2成员4)对于骨骼肌和脂肪细胞摄取葡萄糖至关重要,而骨骼肌和脂肪细胞在全身葡萄糖代谢中发挥着核心作用。在此,我们使用直接随机光学重建显微镜(dSTORM)在单分子水平上研究质膜融合的葡萄糖转运蛋白4的特征,证明了胰岛素和胰岛素抵抗调节脂肪细胞中葡萄糖转运蛋白4的空间组织。胰岛素刺激使质膜上葡萄糖转运蛋白4的平衡向更分散的构型转变。相反,胰岛素抵抗导致葡萄糖转运蛋白4分布更聚集,并增加了每个簇中分子的平均数。此外,我们的数据表明,FQQI基序和脂筏介导了质膜上葡萄糖转运蛋白4簇的维持。FQQI突变(FQQA-葡萄糖转运蛋白4)导致葡萄糖转运蛋白4分布更聚集;此外,在表达FQQA-葡萄糖转运蛋白4的脂肪细胞中破坏脂筏显著降低了大簇的百分比和每个簇中分子的平均数。总之,我们的数据阐明了胰岛素刺激或胰岛素抵抗对质膜上葡萄糖转运蛋白4重组的影响,并揭示了胰岛素抵抗的新致病机制。