TY - JOUR
T1 - Granzyme B can cause mitochondrial depolarization and cell death in the absence of BID, BAX, and BAK
AU - Thomas, Dori A.
AU - Scorrano, Luca
AU - Putcha, Girish V.
AU - Korsmeyer, Stanley J.
AU - Ley, Timothy J.
PY - 2001/12/18
Y1 - 2001/12/18
N2 - Granzyme B (GzmB) is a serine protease that is used by activated cytotoxic 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.
AB - Granzyme B (GzmB) is a serine protease that is used by activated cytotoxic 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.
UR - http://www.scopus.com/inward/record.url?scp=0035910057&partnerID=8YFLogxK
U2 - 10.1073/pnas.261581498
DO - 10.1073/pnas.261581498
M3 - Article
C2 - 11752447
AN - SCOPUS:0035910057
SN - 0027-8424
VL - 98
SP - 14985
EP - 14990
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 26
ER -