Lauritzen Hans P M M, Galbo Henrik, Brandauer Josef, Goodyear Laurie J, Ploug Thorkil
Research Division, Joslin Diabetes Center and Harvard Medical School, Boston, MA 02215, USA.
Diabetes. 2008 Feb;57(2):315-24. doi: 10.2337/db06-1578. Epub 2007 Oct 31.
Insulin stimulates glucose transport in skeletal muscle by GLUT4 translocation from intracellular compartments to sarcolemma and t-tubules. We studied in living animals the recruitment of GLUT4 vesicles in more detail than previously done and, for the first time, analyzed the steady-state recycling and subsequent re-internalization of GLUT4 on an insulin bolus.
A confocal imaging technique was used in GLUT4-enhanced green fluorescent protein-transfected superficial muscle fibers in living mice.
During the first 30 min of insulin stimulation, very few superficially or deeply located GLUT4 storage vesicles (>1 microm) moved in toto. Rather, big vesicles were stationary in their original position at sarcolemma or t-tubules and were locally depleted of GLUT4 by budding off of smaller vesicles. Photobleaching experiments revealed that during initial translocation and steady-state recycling, GLUT4 microvesicles (<1 microm) move from perinuclear GLUT4 depots out along the plasma membrane. Furthermore, after photobleaching of t-tubule areas, recovery of GLUT4 was slow or absent, indicating no recycling of GLUT4 from perinuclear or adjacent (1 microm) or more distant (20 microm) t-tubule areas. During waning of insulin effect, GLUT4 was re-internalized to basal stores with a delay in t-tubules compared with sarcolemma, probably reflecting delayed disappearance of insulin from t-tubules.
In skeletal muscle, insulin reversibly stimulates local depletion of GLUT4 storage vesicles at sarcolemma and t-tubules rather than inducing movement of intact storage vesicles. During steady-state stimulation, recycling of GLUT4-containing microvesicles over longer distances (10-20 microm) takes place between perinuclear depots and sarcolemma but not at t-tubules.
胰岛素通过葡萄糖转运蛋白4(GLUT4)从细胞内区室转位至肌膜和横管,刺激骨骼肌中的葡萄糖转运。我们在活体动物中比以往更详细地研究了GLUT4囊泡的募集情况,并首次分析了胰岛素推注后GLUT4的稳态再循环及随后的再内化过程。
在转染了GLUT4增强型绿色荧光蛋白的活体小鼠浅表肌纤维中使用共聚焦成像技术。
在胰岛素刺激的最初30分钟内,极少有位于浅表或深部的GLUT4储存囊泡(>1微米)整体移动。相反,大囊泡在肌膜或横管的原始位置静止不动,并通过出芽形成较小的囊泡而局部耗尽GLUT4。光漂白实验表明,在初始转位和稳态再循环过程中,GLUT4微囊泡(<1微米)从核周GLUT4储存库沿质膜向外移动。此外,在横管区域进行光漂白后,GLUT4的恢复缓慢或未发生,表明GLUT4没有从核周、相邻(1微米)或更远(20微米)的横管区域进行再循环。在胰岛素作用减弱期间,GLUT4再内化至基础储存库,与肌膜相比,横管中的延迟,这可能反映了胰岛素从横管中消失的延迟。
在骨骼肌中,胰岛素可逆地刺激肌膜和横管处GLUT4储存囊泡的局部耗尽,而不是诱导完整储存囊泡的移动。在稳态刺激期间,含GLUT4的微囊泡在核周储存库和肌膜之间进行较长距离(10 - 20微米)的再循环,但在横管处则不然。