Rajan A S, Aguilar-Bryan L, Nelson D A, Yaney G C, Hsu W H, Kunze D L, Boyd A E
Department of Medicine, Baylor College of Medicine, Houston, TX 77030.
Diabetes Care. 1990 Mar;13(3):340-63. doi: 10.2337/diacare.13.3.340.
We review the role of ion channels in regulating insulin secretion from pancreatic beta-cells. By controlling ion permeability, ion channels at the membrane play a major role in regulating both electrical activity and signal transduction in the beta-cell. A proximal step in the cascade of events required for stimulus-secretion coupling is the closure of ATP-sensitive K+ channels, resulting in cell depolarization. Of particular relevance is the finding that this channel is directly regulated by a metabolite of glucose, which is the primary insulin secretagogue. In addition, this channel, or a closely associated protein, contains the sulfonylurea-binding site. Another K+ channel, the Ca2(+)-activated K+ channel, may be involved in cell repolarization to create homeostasis. Voltage-dependent Ca2+ channels are activated by cell depolarization and regulate Ca2+ influx into the cell. By controlling cytosolic free-Ca2+ levels ([Ca2+]i), these channels play an important role in transducing the initial stimulus to the effector systems that modulate insulin secretion. The link between a rise in [Ca2+]i and the terminal event of exocytosis is the least-understood aspect of stimulus-secretion coupling. However, phosphorylation studies have identified substrate proteins that may correspond to those involved in smooth muscle contraction, suggesting an analogy in the processes of stimulus secretion and excitation contraction. The advent of new methodology, particularly the patch-clamp technique, has fostered a more detailed characterization of the beta-cell ion channels. Furthermore, biochemical and molecular approaches developed for the structural analysis of ion channels in other tissues can now be applied to the isolation and characterization of the beta-cell ion channels. This is of particular significance because there appear to be tissue-specific variations in the different types of ion channels. Given the importance of ion channels in cell physiology, a knowledge of the structure and properties of these channels in the beta-cell is required for understanding the abnormalities of insulin secretion that occur in non-insulin-dependent diabetes mellitus. Ultimately, these studies should also provide new therapeutic approaches to the treatment of this disease.
我们综述了离子通道在调节胰腺β细胞胰岛素分泌中的作用。通过控制离子通透性,细胞膜上的离子通道在调节β细胞的电活动和信号转导方面发挥着主要作用。刺激-分泌偶联所需事件级联反应的一个近端步骤是ATP敏感性钾通道的关闭,导致细胞去极化。特别相关的发现是,该通道直接受葡萄糖代谢物的调节,而葡萄糖是主要的胰岛素促分泌剂。此外,该通道或与之密切相关的蛋白质含有磺酰脲结合位点。另一种钾通道,即钙激活钾通道,可能参与细胞复极化以建立内环境稳态。电压依赖性钙通道通过细胞去极化被激活,并调节钙离子流入细胞。通过控制胞质游离钙离子水平([Ca2+]i),这些通道在将初始刺激转导至调节胰岛素分泌的效应系统中发挥重要作用。[Ca2+]i升高与胞吐作用终末事件之间的联系是刺激-分泌偶联中了解最少的方面。然而,磷酸化研究已经确定了可能与平滑肌收缩相关的底物蛋白,这表明刺激分泌和兴奋收缩过程存在相似之处。新方法的出现,特别是膜片钳技术,促进了对β细胞离子通道更详细的表征。此外,为其他组织中离子通道结构分析开发的生化和分子方法现在可应用于β细胞离子通道的分离和表征。这具有特别重要的意义,因为不同类型的离子通道似乎存在组织特异性差异。鉴于离子通道在细胞生理学中的重要性,了解β细胞中这些通道的结构和特性对于理解非胰岛素依赖型糖尿病中发生的胰岛素分泌异常是必要的。最终,这些研究也应为该疾病的治疗提供新的治疗方法。