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Genetic Regulation of RIPK1 and Necroptosis
Annual Review of Genetics ( IF 11.1 ) Pub Date : 2021-11-23 , DOI: 10.1146/annurev-genet-071719-022748
Daichao Xu 1 , Chengyu Zou 1 , Junying Yuan 1
Affiliation  

The receptor-interacting protein kinase 1 (RIPK1) is recognized as a master upstream regulator that controls cell survival and inflammatory signaling as well as multiple cell death pathways, including apoptosis and necroptosis. The activation of RIPK1 kinase is extensively modulated by ubiquitination and phosphorylation, which are mediated by multiple factors that also control the activation of the NF-κB pathway. We discuss current findings regarding the genetic modulation of RIPK1 that controls its activation and interaction with downstream mediators, such as caspase-8 and RIPK3, to promote apoptosis and necroptosis. We also address genetic autoinflammatory human conditions that involve abnormal activation of RIPK1. Leveraging these new genetic and mechanistic insights, we postulate how an improved understanding of RIPK1 biology may support the development of therapeutics that target RIPK1 for the treatment of human inflammatory and neurodegenerative diseases.

中文翻译:


RIPK1 和坏死性凋亡的遗传调控

受体相互作用蛋白激酶 1 (RIPK1) 被认为是一种主要的上游调节因子,可控制细胞存活和炎症信号以及多种细胞死亡途径,包括细胞凋亡和坏死性凋亡。RIPK1 激酶的激活受到泛素化和磷酸化的广泛调节,泛素化和磷酸化由多种因素介导,这些因素也控制 NF-κB 通路的激活。我们讨论了目前关于 RIPK1 的基因调节的发现,该基因调节控制其激活以及与下游介质(如 caspase-8 和 RIPK3)的相互作用,以促进细胞凋亡和坏死性凋亡。我们还解决了涉及 RIPK1 异常激活的遗传性自身炎症性人类疾病。利用这些新的遗传和机制见解,

更新日期:2021-11-24
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