Laboratory of Experimental Medicine, Université Libre de Bruxelles, Route de Lennik, 808, 1070, Brussels, Belgium.
Trends Cell Biol. 2011 Jul;21(7):424-31. doi: 10.1016/j.tcb.2011.03.001. Epub 2011 Apr 12.
Diabetes is a metabolic disease affecting nearly 300 million individuals worldwide. Both types of diabetes (1 and 2) are characterized by loss of functional pancreatic β-cell mass causing different degrees of insulin deficiency. The Bcl-2 family has a double-edged effect in diabetes. These proteins are crucial controllers of the mitochondrial pathway of β-cell apoptosis induced by pro-inflammatory cytokines or lipotoxicity. In parallel, some Bcl-2 members also regulate glucose metabolism and β-cell function. In this review, we describe the role of Bcl-2 proteins in β-cell homeostasis and death. We focus on how these proteins interact, their contribution to the crosstalk between endoplasmic reticulum stress and mitochondrial permeabilization, their context-dependent usage following different pro-apoptotic stimuli, and their role in β-cell physiology.
糖尿病是一种影响全球近 3 亿人口的代谢疾病。1 型和 2 型糖尿病的特征均为功能性胰腺β细胞数量减少,导致不同程度的胰岛素缺乏。Bcl-2 家族在糖尿病中具有双重作用。这些蛋白是促炎细胞因子或脂毒性诱导的β细胞凋亡的线粒体途径的关键调控因子。同时,一些 Bcl-2 成员也调节葡萄糖代谢和β细胞功能。在这篇综述中,我们描述了 Bcl-2 蛋白在β细胞稳态和死亡中的作用。我们重点介绍了这些蛋白如何相互作用,它们对内质网应激和线粒体通透性之间串扰的贡献,以及在不同的促凋亡刺激下它们的上下文相关使用,以及它们在β细胞生理学中的作用。