Guillam M T, Burcelin R, Thorens B
Institute of Pharmacology and Toxicology, University of Lausanne, 27, rue du Bugnon, CH-1005 Lausanne, Switzerland.
Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12317-21. doi: 10.1073/pnas.95.21.12317.
Glucose production by liver is a major physiological function, which is required to prevent development of hypoglycemia in the postprandial and fasted states. The mechanism of glucose release from hepatocytes has not been studied in detail but was assumed instead to depend on facilitated diffusion through the glucose transporter GLUT2. Here, we demonstrate that in the absence of GLUT2 no other transporter isoforms were overexpressed in liver and only marginally significant facilitated diffusion across the hepatocyte plasma membrane was detectable. However, the rate of hepatic glucose output was normal. This was evidenced by (i) the hyperglycemic response to i.p. glucagon injection; (ii) the in vivo measurement of glucose turnover rate; and (iii) the rate of release of neosynthesized glucose from isolated hepatocytes. These observations therefore indicated the existence of an alternative pathway for hepatic glucose output. Using a [14C]-pyruvate pulse-labeling protocol to quantitate neosynthesis and release of [14C]glucose, we demonstrated that this pathway was sensitive to low temperature (12 degreesC). It was not inhibited by cytochalasin B nor by the intracellular traffic inhibitors brefeldin A and monensin but was blocked by progesterone, an inhibitor of cholesterol and caveolae traffic from the endoplasmic reticulum to the plasma membrane. Our observations thus demonstrate that hepatic glucose release does not require the presence of GLUT2 nor of any plasma membrane glucose facilitative diffusion mechanism. This implies the existence of an as yet unsuspected pathway for glucose release that may be based on a membrane traffic mechanism.
肝脏产生葡萄糖是一项主要的生理功能,对于预防餐后和禁食状态下低血糖的发生至关重要。肝细胞释放葡萄糖的机制尚未得到详细研究,而是被认为依赖于通过葡萄糖转运体GLUT2的易化扩散。在此,我们证明在缺乏GLUT2的情况下,肝脏中没有其他转运体异构体过度表达,并且仅能检测到极少量的跨肝细胞膜的易化扩散。然而,肝脏葡萄糖输出率是正常的。这通过以下几点得到证明:(i)腹腔注射胰高血糖素后的高血糖反应;(ii)体内葡萄糖周转率的测量;以及(iii)分离肝细胞中新合成葡萄糖的释放速率。因此,这些观察结果表明存在肝脏葡萄糖输出的替代途径。使用[14C] - 丙酮酸脉冲标记方案来定量[14C]葡萄糖的新合成和释放,我们证明该途径对低温(12℃)敏感。它不受细胞松弛素B的抑制,也不受细胞内运输抑制剂布雷菲德菌素A和莫能菌素的抑制,但被孕酮阻断,孕酮是一种从内质网到质膜的胆固醇和小窝运输的抑制剂。我们的观察结果因此表明,肝脏葡萄糖释放既不需要GLUT2的存在,也不需要任何质膜葡萄糖易化扩散机制。这意味着存在一种尚未被怀疑的葡萄糖释放途径,其可能基于膜运输机制。