Experimental Diabetes, Metabolism, and Nutrition Section, Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Cell Metab. 2010 Sep 8;12(3):250-9. doi: 10.1016/j.cmet.2010.08.005.
While the glucose transporter-4 (GLUT4) is fundamental to insulin-regulated glucose metabolism, its dynamic spatial organization in the plasma membrane (PM) is unclear. Here, using multicolor TIRF microscopy in transfected adipose cells, we demonstrate that insulin regulates not only the exocytosis of GLUT4 storage vesicles but also PM distribution of GLUT4 itself. In the basal state, domains (clusters) of GLUT4 molecules in PM are created by an exocytosis that retains GLUT4 at the fusion site. Surprisingly, when insulin induces a burst of GLUT4 exocytosis, it does not merely accelerate this basal exocytosis but rather stimulates approximately 60-fold another mode of exocytosis that disperses GLUT4 into PM. In contradistinction, internalization of most GLUT4, regardless of insulin, occurs from pre-existing clusters via the subsequent recruitment of clathrin. The data fit a new kinetic model that features multifunctional clusters as intermediates of exocytosis and endocytosis.
葡萄糖转运蛋白-4(GLUT4)对于胰岛素调节的葡萄糖代谢至关重要,但它在质膜(PM)中的动态空间组织尚不清楚。在这里,我们使用转染脂肪细胞中的多色 TIRF 显微镜,证明胰岛素不仅调节 GLUT4 储存囊泡的胞吐作用,还调节 GLUT4 本身在 PM 中的分布。在基础状态下,PM 中 GLUT4 分子的域(簇)是通过保留融合部位 GLUT4 的胞吐作用产生的。令人惊讶的是,当胰岛素诱导 GLUT4 胞吐作用爆发时,它不仅加速了这种基础胞吐作用,而且还刺激了大约 60 倍的另一种胞吐作用模式,将 GLUT4 分散到 PM 中。相比之下,大多数 GLUT4 的内化,无论是否有胰岛素,都是通过网格蛋白的后续募集,从预先存在的簇中发生的。这些数据符合一种新的动力学模型,该模型以多功能簇作为胞吐作用和胞吞作用的中间产物。