Activation of the NF-κB pathway by Caspase 8 and its homologs

被引:202
作者
Chaudhary, PM
Eby, MT
Jasmin, A
Kumar, A
Liu, L
Hood, L
机构
[1] UT, SW Med Ctr, Hamon Ctr Therapeut Oncol Res, Dallas, TX 75390 USA
[2] Univ Washington, Dept Mol Biotechnol, Seattle, WA 98195 USA
关键词
NF-kappa B; caspase; FADD; death effector domain; MRIT; cFLIP;
D O I
10.1038/sj.onc.1203812
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caspase 8 is the most proximal caspase in the caspase cascade and has been known for its role in the mediation of cell death by various death receptors belonging to the TNFR family. We have discovered that Caspase 8 can activate the NF-kappa B pathway independent of its activity as a pro-apoptotic protease, This property is localized to its N-terminal prodomain, which contains two homologous death effector domains (DEDs). Caspase 10 and MRIT, two DEDs-containing homologs of Caspase 8, can similarly activate the NF-kappa B pathway. Dominantnegative mutants of the Caspase 8 prodomain can block NF-kappa B induced by Caspase 8, FADD and several death receptors belonging to the TNFR family. Caspase 8 can interact with multiple proteins known to be involved in the activation of the NF-kappa B pathway, including the serine-threonine kinases RIP, NIK, IKK1 and IKK2, Thus, DEDs-containing caspases and caspase homolog(s) may have functions beyond their known role in the mediation of cell death.
引用
收藏
页码:4451 / 4460
页数:10
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