自噬
程序性细胞死亡
细胞生物学
半胱氨酸蛋白酶
细胞凋亡
激酶
丝氨酸
坏死
生物
蛋白激酶A
信号转导
化学
磷酸化
生物化学
遗传学
作者
Li Yu,Ajjai Alva,Helen C. Su,Parmesh Dutt,Eric C. Freundt,Sarah J. Welsh,Eric H. Baehrecke,Michael J. Lenardo
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2004-05-11
卷期号:304 (5676): 1500-1502
被引量:1212
标识
DOI:10.1126/science.1096645
摘要
Caspases play a central role in apoptosis, a well-studied pathway of programmed cell death. Other programs of death potentially involving necrosis and autophagy may exist, but their relation to apoptosis and mechanisms of regulation remains unclear. We define a new molecular pathway in which activation of the receptor-interacting protein (a serine-threonine kinase) and Jun amino-terminal kinase induced cell death with the morphology of autophagy. Autophagic death required the genes ATG7 and beclin 1 and was induced by caspase-8 inhibition. Clinical therapies involving caspase inhibitors may arrest apoptosis but also have the unanticipated effect of promoting autophagic cell death.
科研通智能强力驱动
Strongly Powered by AbleSci AI