Emerging Roles for RIPK1 and RIPK3 in Pathogen-Induced Cell Death and Host Immunity

被引:15
|
作者
Saleh, Danish [1 ,2 ]
Degterev, Alexei [3 ]
机构
[1] Tufts Univ, Sch Med, Sackler Sch Grad Biomed Sci, Med Scientist Training Program, Boston, MA 02111 USA
[2] Tufts Univ, Sackler Sch Grad Biomed Sci, Program Neurosci, Boston, MA 02111 USA
[3] Tufts Univ, Sch Med, Dept Dev Mol & Chem Biol, Boston, MA 02111 USA
来源
关键词
VIRUS-INFECTED CELLS; TNF-INDUCED NECROSIS; NF-KAPPA-B; YERSINIA-PSEUDOTUBERCULOSIS; PROGRAMMED NECROSIS; APOPTOSIS; NECROPTOSIS; KINASE; MACROPHAGES; ALPHA;
D O I
10.1007/82_2015_449
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Receptor-interacting protein kinases 1 and 3 (RIPK1 and RIPK3) are homologous serine-threonine kinases that were recognized for their roles in directing programmed necrotic cell death or necroptosis under a broad range of pathologic settings. Emerging evidence suggests new physiologic roles for RIPK1 and RIPK3 in mediating cell death of innate immune responses. Our review discusses current evidence on the mechanisms and the impact of RIPK1- and/or RIPK3-dependent cell death in responses to a variety of viral and bacterial pathogens. Furthermore, the discussion also summarizes emerging roles for RIPK1 and RIPK3 in other facets of host immunity, including the maintenance of epithelial barrier function and pro-inflammatory processes that may, in some cases, manifest independent of cell death. Finally, we briefly consider the therapeutic opportunities in targeting RIPK1- and RIPK3-dependent processes in infection and immunity.
引用
收藏
页码:37 / 75
页数:39
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