Mikhailov Valery, Mikhailova Margarita, Degenhardt Kurt, Venkatachalam Manjeri A, White Eileen, Saikumar Pothana
Department of Pathology, The University of Texas Health Science Center, San Antonio, Texas 78229, USA.
J Biol Chem. 2003 Feb 14;278(7):5367-76. doi: 10.1074/jbc.M203392200. Epub 2002 Nov 25.
ATP depletion induced by hypoxia or mitochondrial inhibitors results in Bax translocation from cytosol to mitochondria and release of cytochrome c from mitochondria into cytosol in cultured rat proximal tubule cells. Translocated Bax undergoes further conformational changes to oligomerize into high molecular weight complexes (Mikhailov, V., Mikhailova, M., Pulkrabek, D. J., Dong, Z., Venkatachalam, M. A., and Saikumar, P. (2001) J. Biol. Chem. 276, 18361-18374). Here we report that following Bax translocation in ATP-depleted rat proximal tubule cells, Bak, a proapoptotic molecule that normally resides in mitochondria, also reorganizes to form homo-oligomers. Oligomerization of both Bax and Bak occurred independently of Bid cleavage and/or translocation. Western blots of chemically cross-linked membrane extracts showed nonoverlapping "ladders" of Bax and Bak complexes in multiples of approximately 21 and approximately 23 kDa, respectively, consistent with molecular homogeneity within each ladder. This indicated that Bax and Bak complexes were homo-oligomeric. Nevertheless, each oligomer could be co-immunoprecipitated with the other, suggesting a degree of affinity between Bax and Bak that permitted co-precipitation but not cross-linking. Furthermore, dissociation of cross-linked complexes by SDS and renaturation prior to immunoprecipitation did not prevent reassociation of the two oligomeric species. Notably, expression of Bcl-2 prevented not only the oligomerization of Bax and Bak, but also the association between these two proteins in energy-deprived cells. Using Bax-deficient HCT116 and BMK cells, we show that there is stringent Bax requirement for Bak homo-oligomerization and for cytochrome c release during energy deprivation. Using Bak-deficient BMK cells we further show that Bak deficiency is associated with delayed kinetics of Bax translocation but does not affect either the oligomerization of translocated Bax or the leakage of cytochrome c. These results suggest a degree of functional cooperation between Bax and Bak in this form of cell injury, but also demonstrate an absolute requirement of Bax for mitochondrial permeabilization.
缺氧或线粒体抑制剂诱导的ATP耗竭导致培养的大鼠近端肾小管细胞中Bax从胞质溶胶转位至线粒体,以及细胞色素c从线粒体释放到胞质溶胶中。转位的Bax会进一步发生构象变化,聚合成高分子量复合物(米哈伊洛夫,V.,米哈伊洛娃,M.,普尔克拉贝克,D. J.,董,Z.,文卡塔查拉姆,M. A.,以及赛库马尔,P.(2001年)《生物化学杂志》276,18361 - 18374)。在此我们报告,在ATP耗竭的大鼠近端肾小管细胞中Bax转位后,正常定位于线粒体的促凋亡分子Bak也会重新组织形成同源寡聚体。Bax和Bak的寡聚化独立于Bid的切割和/或转位发生。化学交联膜提取物的蛋白质免疫印迹显示,Bax和Bak复合物分别形成倍数约为21 kDa和约23 kDa的不重叠“条带”,这与每个条带内的分子同质性一致。这表明Bax和Bak复合物是同源寡聚体。然而,每个寡聚体都能与另一个进行共免疫沉淀,这表明Bax和Bak之间存在一定程度的亲和力,允许共沉淀但不允许交联。此外,在免疫沉淀之前用SDS解离交联复合物并使其复性,并不会阻止这两种寡聚体的重新结合。值得注意的是,Bcl - 2的表达不仅阻止了Bax和Bak的寡聚化,还阻止了能量剥夺细胞中这两种蛋白质之间的结合。使用缺乏Bax的HCT116和BMK细胞,我们发现能量剥夺期间Bak同源寡聚化和细胞色素c释放严格依赖Bax。使用缺乏Bak的BMK细胞,我们进一步表明Bak缺乏与Bax转位的延迟动力学相关,但不影响转位Bax的寡聚化或细胞色素c的泄漏。这些结果表明在这种形式的细胞损伤中Bax和Bak之间存在一定程度的功能协作,但也证明了线粒体通透性转换绝对需要Bax。