Raynal P, Pollard H B, Cushman S W, Guerre-Millo M
Laboratory of Cell Biology and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Biochem Biophys Res Commun. 1996 Aug 5;225(1):116-21. doi: 10.1006/bbrc.1996.1139.
Several lines of evidence suggest that annexins, a family of phospholipid-binding proteins, play a role in cellular trafficking. Five annexins (I, II, V, VI, VII) were detected in rat adipose cells. They were primarily associated with the plasma membrane in a calcium-dependent manner. None of them redistributed with insulin treatment of the cells, in contrast to the glucose transporter GLUT4, which moved from intracellular membranes to the plasma membrane. Although the actual function of annexins in adipose cells remains to be determined, our data indicate that insulin-stimulated GLUT4 trafficking does not rely on a change in subcellular location of any of the five annexins detected so far in these cells.
多项证据表明,膜联蛋白(一类磷脂结合蛋白)在细胞运输中发挥作用。在大鼠脂肪细胞中检测到了五种膜联蛋白(I、II、V、VI、VII)。它们主要以钙依赖的方式与质膜相关联。与葡萄糖转运蛋白GLUT4不同,用胰岛素处理细胞时,这些膜联蛋白均不会重新分布,GLUT4会从细胞内膜转移到质膜。尽管膜联蛋白在脂肪细胞中的实际功能仍有待确定,但我们的数据表明,胰岛素刺激的GLUT4运输并不依赖于迄今为止在这些细胞中检测到的五种膜联蛋白中任何一种的亚细胞定位变化。