Multitasking Kinase RIPK1 Regulates Cell Death and Inflammation

被引:72
作者
Newton, Kim [1 ]
机构
[1] Genentech Inc, Dept Physiol Chem, San Francisco, CA 94080 USA
关键词
NF-KAPPA-B; RECEPTOR-INTERACTING PROTEIN; NECROSIS-FACTOR RECEPTOR; MIXED LINEAGE KINASE; TANK-BINDING KINASE-1; SPATA2 LINKS CYLD; PROGRAMMED NECROSIS; DOMAIN-LIKE; PSEUDOKINASE MLKL; CUTTING EDGE;
D O I
10.1101/cshperspect.a036368
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Receptor-interacting serine threonine kinase 1 (RIPK1) is a widely expressed kinase that is essential for limiting inflammation in both mice and humans. Mice lacking RIPK1 die at birth from multiorgan inflammation and aberrant cell death, whereas humans lacking RIPK1 are immunodeficient and develop very early-onset inflammatory bowel disease. In contrast to complete loss of RIPK1, inhibiting the kinase activity of RIPK1 genetically or pharmacologically prevents cell death and inflammation in several mouse disease models. Indeed, small molecule inhibitors of RIPK1 are in phase I clinical trials for amyotrophic lateral sclerosis, and phase H clinical trials for psoriasis, rheumatoid arthritis, and ulcerative colitis. This review focuses on which signaling pathways use RIPK1, how activation of RIPK1 is regulated, and when activation of RIPK1 appears to be an important driver of inflammation.
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页数:21
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