Davey Katherine A B, Garlick Pamela B, Warley Alice, Southworth Richard
Division of Imaging Sciences, Guy's, King's, and St. Thomas' School of Medicine, King's College London, London, United Kingdom.
Am J Physiol Heart Circ Physiol. 2007 Apr;292(4):H2009-19. doi: 10.1152/ajpheart.00663.2006. Epub 2006 Dec 22.
Whereas glucose transporter 1 (GLUT-1) is thought to be responsible for basal glucose uptake in cardiac myocytes, little is known about its relative distribution between the different plasma membranes and cell types in the heart. GLUT-4 translocates to the myocyte surface to increase glucose uptake in response to a number of stimuli. The mechanisms underlying ischemia- and insulin-mediated GLUT-4 translocation are known to be different, raising the possibility that the intracellular destinations of GLUT-4 following these stimuli also differ. Using immunogold labeling, we describe the cellular localization of these two transporters and investigate whether insulin and ischemia induce differential translocation of GLUT-4 to different cardiac membranes. Immunogold labeling of GLUT-1 and GLUT-4 was performed on left ventricular sections from isolated hearts following 30 min of either insulin, ischemia, or control perfusion. In control tissue, GLUT-1 was predominantly (76%) localized in the capillary endothelial cells, with only 24% of total cardiac GLUT-1 present in myocytes. GLUT-4 was found predominantly in myocytes, distributed between sarcolemmal and T tubule membranes (1.84 +/- 0.49 and 1.54 +/- 0.33 golds/microm, respectively) and intracellular vesicles (127 +/- 18 golds/microm(2)). Insulin increased T tubule membrane GLUT-4 content (2.8 +/- 0.4 golds/microm, P < 0.05) but had less effect on sarcolemmal GLUT-4 (1.72 +/- 0.53 golds/microm). Ischemia induced greater GLUT-4 translocation to both membrane types (4.25 +/- 0.84 and 4.01 +/- 0.27 golds/microm, respectively P < 0.05). The localization of GLUT-1 suggests a significant role in transporting glucose across the capillary wall before myocyte uptake via GLUT-1 and GLUT-4. We demonstrate independent spatial translocation of GLUT-4 under insulin or ischemic stimulation and propose independent roles for T-tubular and sarcolemmal GLUT-4.
虽然葡萄糖转运蛋白1(GLUT-1)被认为负责心肌细胞的基础葡萄糖摄取,但对于其在心脏不同质膜和细胞类型之间的相对分布却知之甚少。GLUT-4会响应多种刺激而转位到心肌细胞表面,以增加葡萄糖摄取。已知缺血和胰岛素介导的GLUT-4转位机制不同,这增加了这些刺激后GLUT-4的细胞内目的地也不同的可能性。我们使用免疫金标记来描述这两种转运蛋白的细胞定位,并研究胰岛素和缺血是否会诱导GLUT-4向不同心脏膜的差异转位。在胰岛素、缺血或对照灌注30分钟后,对离体心脏的左心室切片进行GLUT-1和GLUT-4的免疫金标记。在对照组织中,GLUT-1主要(76%)定位于毛细血管内皮细胞,心肌细胞中仅存在24%的心脏总GLUT-1。GLUT-4主要存在于心肌细胞中,分布在肌膜和T小管膜之间(分别为1.84±0.49和1.54±0.33个金颗粒/微米)以及细胞内囊泡中(127±18个金颗粒/微米²)。胰岛素增加了T小管膜GLUT-4含量(2.8±0.4个金颗粒/微米,P<0.05),但对肌膜GLUT-4的影响较小(1.72±0.53个金颗粒/微米)。缺血诱导更多的GLUT-4转位到这两种膜类型(分别为4.25±0.84和4.01±0.27个金颗粒/微米,P<0.05)。GLUT-1的定位表明其在通过GLUT-1和GLUT-4进行心肌细胞摄取之前,在跨毛细血管壁转运葡萄糖方面发挥重要作用。我们证明了在胰岛素或缺血刺激下GLUT-4的独立空间转位,并提出了T小管和肌膜GLUT-4的独立作用。