坏死性下垂
裂谷1
程序性细胞死亡
细胞生物学
激酶
细胞凋亡
蛋白激酶A
癌症研究
化学
生物
生物化学
作者
Kim Newton,Debra L. Dugger,Katherine E. Wickliffe,Neeraj Kapoor,M. Cristina de Almagro,Domagoj Vucic,László G. Kömüves,Ronald E. Ferrando,Dorothy French,Joshua D. Webster,Merone Roose‐Girma,Søren Warming,Vishva M. Dixit
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2014-02-21
卷期号:343 (6177): 1357-1360
被引量:606
标识
DOI:10.1126/science.1249361
摘要
Life and Cell Death Trying to protect animals from one form of cell death may lead to death by another. Two protein kinases, known as RIPK1 and RIPK3 promote signaling that leads to cell death by necroptosis. However, Newton et al. (p. 1357 , published online 20 February; see the Perspective by Zhang and Chan ) found that inhibition of RIPK3 was not always beneficial. Instead, mice expressing a form of RIPK3 with no catalytic activity died from increased apoptotic cell death, but animals lacking the RIPK3 protein entirely, did not die perhaps because RIPK3 restrains apoptosis mediated by caspase-8 by an independent mechanism.
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