Shoshan-Barmatz Varda, Keinan Nurit, Zaid Hilal
Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
J Bioenerg Biomembr. 2008 Jun;40(3):183-91. doi: 10.1007/s10863-008-9147-9.
Proper cell activity requires an efficient exchange of molecules between mitochondria and cytoplasm. Lying in the outer mitochondrial membrane, VDAC assumes a crucial position in the cell, forming the main interface between the mitochondrial and the cellular metabolisms. As such, it has been recognized that VDAC plays a crucial role in regulating the metabolic and energetic functions of mitochondria. Indeed, down-regulation of VDAC1 expression by shRNA leads to a decrease in energy production and cell growth. VDAC has also been recognized as a key protein in mitochondria-mediated apoptosis through its involvement in the release of apoptotic proteins located in the inter-membranal space and as the proposed target of pro- and anti-apoptotic members of the Bcl2-family and of hexokinase. Questions, however, remain as to if and how VDAC mediates the transfer of apoptotic proteins from the inter-membranal space to the cytosol. The diameter of the VDAC pore is only about 2.5-3 nm, insufficient for the passage of a folded protein like cytochrome c. New work, however, suggests that pore formation involves the assembly of homo-oligomers of VDAC or hetero-oligomers composed of VDAC and pro-apoptotic proteins, such as Bax. Thus, VDAC appears to represent a convergence point for a variety of cell survival and cell death signals. This review provides insight into the central role of VDAC in mammalian cell life and death, emphasizing VDAC function in the regulation of mitochondria-mediated apoptosis and, as such, its potential as a rational target for new therapeutics.
正常的细胞活动需要线粒体与细胞质之间高效地交换分子。位于线粒体外膜的电压依赖性阴离子通道(VDAC)在细胞中占据关键位置,形成线粒体与细胞代谢之间的主要界面。因此,人们已经认识到VDAC在调节线粒体的代谢和能量功能方面起着至关重要的作用。事实上,通过短发夹RNA(shRNA)下调VDAC1的表达会导致能量产生和细胞生长减少。VDAC还因其参与位于膜间隙的凋亡蛋白的释放,以及作为Bcl2家族促凋亡和抗凋亡成员及己糖激酶的假定靶点,而被认为是线粒体介导的凋亡中的关键蛋白。然而,关于VDAC是否以及如何介导凋亡蛋白从膜间隙转移到细胞质溶胶的问题仍然存在。VDAC孔的直径仅约2.5 - 3纳米,不足以让像细胞色素c这样的折叠蛋白通过。然而,新的研究表明,孔的形成涉及VDAC同型寡聚体或由VDAC和促凋亡蛋白(如Bax)组成的异型寡聚体的组装。因此,VDAC似乎代表了多种细胞存活和细胞死亡信号的汇聚点。本综述深入探讨了VDAC在哺乳动物细胞生死中的核心作用,强调了VDAC在调节线粒体介导的凋亡中的功能,以及其作为新治疗靶点的潜力。