坏死性下垂
裂谷1
细胞生物学
生物
程序性细胞死亡
激酶
蛋白激酶A
信号转导
细胞凋亡
癌症研究
生物化学
作者
Ricardo Weinlich,Andrew Oberst,Helen M. Beere,Green
摘要
In the early 2000s, receptor-interacting serine/threonine protein kinase 1 (RIPK1), a molecule already recognized as an important regulator of cell survival, inflammation and disease, was attributed an additional function: the regulation of a novel cell death pathway that came to be known as necroptosis. Subsequently, the related kinase RIPK3 and its substrate mixed-lineage kinase domain-like protein (MLKL) were also implicated in the necroptotic pathway, and links between this pathway and apoptosis were established. In this Timeline article, we outline the discoveries that have helped to identify the roles of RIPK1, RIPK3, MLKL and other regulators of necroptosis, and how they interact to determine cell fate.
科研通智能强力驱动
Strongly Powered by AbleSci AI