Interfaculty Institute of Biochemistry, Tübingen University, Germany.
Max-Planck Institute for Intelligent Systems, Stuttgart, Germany.
FEBS J. 2018 Feb;285(3):416-431. doi: 10.1111/febs.14186. Epub 2017 Sep 4.
Bax and Bak are members of the Bcl-2 family and core regulators of the intrinsic pathway of apoptosis. Upon apoptotic stimuli, they are activated and oligomerize at the mitochondrial outer membrane (MOM) to mediate its permeabilization, which is considered a key step in apoptosis. However, the molecular mechanism underlying Bax and Bak function has remained a key question in the field. Here, we review recent structural and biophysical evidence that has changed our understanding of how Bax and Bak promote MOM permeabilization. We also discuss how the spatial regulation of Bcl-2 family preference for binding partners contributes to regulate Bax and Bak activation. Finally, we consider the contribution of mitochondrial composition, dynamics and interaction with other organelles to apoptosis commitment. A new perspective is emerging, in which the control of apoptosis by Bax and Bak goes beyond them and is highly influenced by additional mitochondrial components.
Bax 和 Bak 是 Bcl-2 家族的成员,也是细胞凋亡内在途径的核心调节因子。在凋亡刺激下,它们在线粒体外膜(MOM)处被激活并寡聚化,从而介导其通透性,这被认为是细胞凋亡的关键步骤。然而,Bax 和 Bak 功能的分子机制一直是该领域的一个关键问题。在这里,我们回顾了最近的结构和生物物理证据,这些证据改变了我们对 Bax 和 Bak 如何促进 MOM 通透性的理解。我们还讨论了 Bcl-2 家族对结合伙伴的偏好的空间调节如何有助于调节 Bax 和 Bak 的激活。最后,我们考虑了线粒体组成、动态和与其他细胞器相互作用对细胞凋亡的影响。一种新的观点正在出现,即 Bax 和 Bak 对细胞凋亡的控制不仅限于它们本身,而且还受到其他线粒体成分的高度影响。