| Literature DB >> 12776182 |
Anne Devin1, Yong Lin, Zheng-gang Liu.
Abstract
The death-domain kinase RIP (receptor-interacting protein) is an important effector of tumour necrosis factor (TNF) signalling and is essential for TNF-induced nuclear factor-kappaB activation. However, the function of RIP in the TNF-induced activation of mitogen-activated protein kinases (MAPKs) has not been fully investigated. In this report, using Rip null (Rip(-/-)) mouse fibroblast cells, we investigated whether RIP is required for TNF-induced activation of the MAPKs extracellular-signal-related kinase (ERK), p38 and c-Jun amino-terminal kinase (JNK). We found that TNF-induced activation of ERK, p38 and JNK is decreased in Rip(-/-) cells. The activation of these kinases by interleukin-1 is normal in Rip(-/-) cells. More importantly, we showed that the kinase activity of RIP is needed for ERK activation.Entities:
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Year: 2003 PMID: 12776182 PMCID: PMC1319199 DOI: 10.1038/sj.embor.embor854
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807