Keeble James A, Gilmore Andrew P
Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, A.3034 Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
Cell Res. 2007 Dec;17(12):976-84. doi: 10.1038/cr.2007.101.
Most defective and unwanted cells die by apoptosis, an exquisitely controlled genetic programme for removing such cells without damaging the surrounding tissue. Once a cell has committed to apoptosis, the process is remarkably efficient, and is completed within a few minutes of initiation. This point of no return for an apoptotic cell is commonly held to be the point at which the outer mitochondrial membrane is permeabilised, a process regulated by the Bcl-2 family of proteins. How these proteins regulate this decision point is central to diseases such as cancer where apoptotic control is lost. In this review, we will discuss apoptotic signalling and how a cell makes the irreversible decision to die. We will focus on one set of survival signals, those derived by cell adhesion to the extracellular matrix (ECM), and use these to highlight the complexities of apoptotic signalling. In particular, we will illustrate how multiple signalling pathways converge to determine critical cell fate decisions.
大多数有缺陷和不需要的细胞通过凋亡死亡,凋亡是一种精确控制的遗传程序,用于清除此类细胞而不损伤周围组织。一旦细胞开始凋亡,这个过程就非常高效,并且在启动后的几分钟内完成。凋亡细胞的这个不可逆转的点通常被认为是线粒体外膜通透性增加的点,这一过程由Bcl-2蛋白家族调节。这些蛋白质如何调节这个决定点是诸如癌症等凋亡控制丧失的疾病的核心问题。在这篇综述中,我们将讨论凋亡信号传导以及细胞如何做出不可逆的死亡决定。我们将重点关注一组存活信号,即细胞与细胞外基质(ECM)粘附所产生的信号,并利用这些信号来突出凋亡信号传导的复杂性。特别是,我们将说明多个信号通路如何汇聚以决定关键的细胞命运。