作者: Tom Vanden Berghe , Behrouz Hassannia , Peter Vandenabeele
DOI: 10.1007/S00018-016-2189-Y
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摘要: Necroptosis was initially identified as a backup cell death program when apoptosis is blocked. However, it now recognized cellular defense mechanism against infections and presumed to be detrimental factor in several pathologies driven by death. prototypic form of regulated necrosis that depends on activation the necrosome, which protein complex receptor interacting kinase (RIPK) 3 activated. The RIP homotypic interaction motif (RHIM) core domain regulates necrosome. To date, three RHIM-containing proteins have been reported activate activity RIPK3 within necrosome: RIPK1, Toll/IL-1 domain-containing adaptor inducing IFN-β (TRIF), DNA-dependent activator interferon regulatory factors (DAI). Here, we review discuss commonalities differences increasing number activators Since discovery mixed lineage domain-like (MLKL) crucial necroptosis, interest has increased monitoring therapeutically targeting their activation. availability new phospho-specific antibodies, pharmacologic inhibitors, transgenic models will allow us further document role necroptosis degenerative, inflammatory infectious diseases.