Granzyme B can cause mitochondrial depolarization and cell death in the absence of BID, BAX, and BAK

被引:98
作者
Thomas, DA
Scorrano, L
Putcha, GV
Korsmeyer, SJ
Ley, TJ
机构
[1] Washington Univ, Sch Med, Div Oncol, Dept Med,Siteman Canc Ctr, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Oncol, Dept Genet,Siteman Canc Ctr, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Howard Hughes Med Inst,Dept Pathol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Howard Hughes Med Inst,Dept Med, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.261581498
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Granzyme B (GzmB) is a serine protease that is used by activated cytoltoxic T lymphocytes to induce target cell apoptosis. Although GzmB directly cleaves the Bcl2 family member BID on target cell entry, Bid-deficient (and Bax, Bak doubly deficient) cells are susceptible to GzmB-induced death, even though they fail to release cytochrome c from mitochondria. GzmB still induces mitochondrial depolarization in Bax, Bak double knockout cells without cytochrome c release or opening of the permeability transition pore. Because GzmB cannot directly cause depolarization of isolated mitochondria, novel intracellular factor(s) may be required for GzmB to depolarize mitochondria in situ. GzmB therefore utilizes two distinct mitochondrial pathways to amplify the proapoptotic signal that it delivers to target cells.
引用
收藏
页码:14985 / 14990
页数:6
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