Funaki Makoto, DiFransico Lesley, Janmey Paul A
Department of Physiology, Institute for Medicine and Engineering, University of Pennsylvania, 1080 Vagelos Research Laboratories, 3340 Smith Walk, Philadelphia, 19104, USA.
Biochim Biophys Acta. 2006 Aug;1763(8):889-99. doi: 10.1016/j.bbamcr.2006.05.012. Epub 2006 May 24.
Insulin-stimulated glucose uptake through GLUT4 plays a pivotal role in maintaining normal blood glucose levels. Glucose transport through GLUT4 requires both GLUT4 translocation to the plasma membrane and GLUT4 activation at the plasma membrane. Here we report that a cell-permeable phosphoinositide-binding peptide, which induces GLUT4 translocation without activation, sequestered PI 4,5-P2 in the plasma membrane from its binding partners. Restoring PI 4,5-P2 to the plasma membrane after the peptide treatment increased glucose uptake. No additional glucose transporters were recruited to the plasma membrane, suggesting that the increased glucose uptake was attributable to GLUT4 activation. Cells overexpressing phosphatidylinositol-4-phosphate 5-kinase treated with the peptide followed by its removal exhibited a higher level of glucose transport than cells stimulated with a submaximal level of insulin. However, only cells treated with submaximal insulin exhibited translocation of the PH-domains of the general receptor for phosphoinositides (GRP1) to the plasma membrane. Thus, PI 4,5-P2, but not PI 3,4,5-P3 converted from PI 4,5-P2, induced GLUT4 activation. Inhibiting F-actin remodeling after the peptide treatment significantly impaired GLUT4 activation induced either by PI 4,5-P2 or by insulin. These results suggest that PI 4,5-P2 in the plasma membrane acts as a second messenger to activate GLUT4, possibly through F-actin remodeling.
胰岛素通过GLUT4刺激葡萄糖摄取在维持正常血糖水平中起关键作用。通过GLUT4进行的葡萄糖转运既需要GLUT4转运至质膜,也需要GLUT4在质膜上被激活。在此我们报告,一种可穿透细胞的磷酸肌醇结合肽,它能诱导GLUT4转运而不激活,将质膜中的PI 4,5-P2与其结合伙伴隔离。肽处理后将PI 4,5-P2恢复到质膜可增加葡萄糖摄取。没有额外的葡萄糖转运体被招募至质膜,这表明增加的葡萄糖摄取归因于GLUT4的激活。用该肽处理过表达磷脂酰肌醇-4-磷酸5-激酶的细胞,随后去除该肽,其葡萄糖转运水平高于用次最大剂量胰岛素刺激的细胞。然而,只有用次最大剂量胰岛素处理的细胞显示磷酸肌醇通用受体(GRP1)的PH结构域转位至质膜。因此,是PI 4,5-P2而非由PI 4,5-P2转化而来的PI 3,4,5-P3诱导了GLUT4的激活。肽处理后抑制F-肌动蛋白重塑显著损害了由PI 4,5-P2或胰岛素诱导的GLUT4激活。这些结果表明,质膜中的PI 4,5-P2可能通过F-肌动蛋白重塑作为激活GLUT4的第二信使。