Valentijn Anthony J, Metcalfe Anthony D, Kott Jane, Streuli Charles H, Gilmore Andrew P
Wellcome Trust Centre for Cell Matrix Research, School of Biological Sciences, University of Manchester, 3.35 Stopford Building, Oxford Road, Manchester M13 9PT, UK.
J Cell Biol. 2003 Aug 18;162(4):599-612. doi: 10.1083/jcb.200302154.
Bax, a member of the Bcl-2 family, translocates to mitochondria during apoptosis, where it forms oligomers which are thought to release apoptogenic factors such as cytochrome c. Using anoikis as a model system, we have examined spatial and temporal changes in Bax distribution. Bax translocates to mitochondria within 15 min of detaching cells from extracellular matrix, but mitochondrial permeabilization does not occur for a number of hours. The formation of Bax oligomers and perimitochondrial clusters occurs concomitant with caspase activation and loss of mitochondrial membrane potential, before nuclear condensation. Cells can be rescued from apoptosis if they are replated onto extracellular matrix within an hour, whereas cells detached for longer could not. The loss of ability to rescue cells from anoikis occurs after Bax translocation, but before the formation of clusters and cytochrome c release. Our data suggest that Bax regulation occurs at several levels, with formation of clusters a late event, and with critical changes determining cell fate occurring earlier.
Bax是Bcl-2家族的成员之一,在细胞凋亡过程中会转位至线粒体,在那里它形成寡聚体,据认为这些寡聚体会释放诸如细胞色素c等促凋亡因子。我们以失巢凋亡作为模型系统,研究了Bax分布的时空变化。在将细胞从细胞外基质分离后的15分钟内,Bax转位至线粒体,但线粒体通透性转变在数小时内都不会发生。Bax寡聚体和线粒体外周簇的形成与半胱天冬酶激活以及线粒体膜电位丧失同时发生,且发生在核浓缩之前。如果在一小时内将细胞重新接种到细胞外基质上,细胞可以从凋亡中被挽救,而分离更长时间的细胞则无法被挽救。从失巢凋亡中挽救细胞的能力丧失发生在Bax转位之后,但在簇形成和细胞色素c释放之前。我们的数据表明,Bax的调控发生在多个层面,簇的形成是一个晚期事件,而决定细胞命运的关键变化发生得更早。