坏死性下垂
裂谷1
炎症
细胞生物学
生物
程序性细胞死亡
特里夫
激酶
信号转导
受体
发病机制
细胞凋亡
肿瘤坏死因子α
免疫学
Toll样受体
先天免疫系统
遗传学
作者
Manolis Pasparakis,Peter Vandenabeele
出处
期刊:Nature
[Nature Portfolio]
日期:2015-01-13
卷期号:517 (7534): 311-320
被引量:1749
摘要
Regulated cell death has essential functions in development and in adult tissue homeostasis. Necroptosis is a newly discovered pathway of regulated necrosis that requires the proteins RIPK3 and MLKL and is induced by death receptors, interferons, toll-like receptors, intracellular RNA and DNA sensors, and probably other mediators. RIPK1 has important kinase-dependent and scaffolding functions that inhibit or trigger necroptosis and apoptosis. Mouse-model studies have revealed important functions for necroptosis in inflammation and suggested that it could be implicated in the pathogenesis of many human inflammatory diseases. We discuss the mechanisms regulating necroptosis and its potential role in inflammation and disease.
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