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Specific ablation of the apoptotic functions of cytochrome c reveals a differential requirement for cytochrome c and apaf-1 in apoptosis
被引:234
作者:
Hao, ZY
[1
]
Duncan, GS
Chang, CC
Elia, A
Fang, M
Wakeham, A
Okada, H
Calzascia, T
Jang, YJ
Annick, YT
Yeh, WC
Ohashi, P
Wang, XD
Mak, TW
机构:
[1] Univ Toronto, Campbell Family Inst Breast Canc Res, Toronto, ON M5G 2C1, Canada
[2] Univ Toronto, Ontario Canc Inst, Univ Hlth Network, Toronto, ON, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON, Canada
[4] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[5] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Dallas, TX 75390 USA
[6] Univ Texas, SW Med Ctr, Dept Biochem, Dallas, TX 75390 USA
来源:
关键词:
D O I:
10.1016/j.cell.2005.03.016
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
As components of the apoptosome, a caspase-activating complex, cytochrome c (Cyt c) and Apaf-1 are thought to play critical roles during apoptosis. Due to the obligate function of Cyt c in electron transport, its requirement for apoptosis in animals has been difficult to establish. We generated "knockin" mice expressing a mutant Cyt c (KA allele), which retains normal electron transfer function but fails to activate Apaf-1. Most KA/KA mice displayed embryonic or perinatal lethality caused by defects in the central nervous system, and surviving mice exhibited impaired lymphocyte homeostasis. Although fibroblasts from the KA/KA mice were resistant to apoptosis, their thymocytes were markedly more sensitive to death stimuli than Apaf-1(-/-) thymocytes. Upon treatment with gamma irradiation, procaspases were efficiently activated in apoptotic KA/KA thymocytes, but Apaf-1 oligomerization was not observed. These studies indicate the existence of a Cyt c- and apoptosome-independent but Apaf-1-dependent mechanism(s) for caspase activation.
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页码:579 / 591
页数:13
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