| created | [InstanceEdit:1267803] Shamovsky, V, 2011-05-09 |
| dbId | 1267801 |
| displayName | In mammals, virus-triggered RIG-1 or MDA5 receptor complex h... |
| literatureReference |
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| modified | [InstanceEdit:1273407] Shamovsky, V, 2011-05-11 |
| schemaClass | Summation |
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In mammals, virus-triggered RIG-1 or MDA5 receptor complex has been shown to recruit initiator caspases-8 and -10 via adapter FADD (Fas-associated death domain-containing protein) leading to NF-kB activation [Takahashi K et al 2006]. Other FADD and caspase-interacting adaptors - RIP-1(receptor interacting protein-1) and TRADD (TNFR-associated death domain) - have been also implicated in RLR-dependent antiviral responses [Kawai T et al 2005, Balachandran M et al 2004, Michallet MC et al 2008]. FADD, TRADD and RIP-1 form signaling complexes that coordinate both apoptotic and non-apoptotic functions of caspases. It has been suggested that large prodomains with DED (death effector domains) of caspases-8/10 can function as a bridge to link downstream mediators like IKK complex to the adaptor proteins [Chaudhary PM et al 2000, Lamkanfi M et al 2006]. Recruitment of caspases-8/10 to activated receptor complex is also believed to result in conformational changes leading to caspase auto-proteolysis. Processed caspases were shown to activate NF-kB signaling. However, the detailed mechanism of caspase-mediated NF-kB induction remains unclear [Takahashi K et al 2006, Lamkanfi M et al 2006]. |
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