Crossref journal-article
Springer Science and Business Media LLC
EMBO reports (297)
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‐κB 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.

Bibliography

Devin, A., Lin, Y., & Liu, Z. (2003). The role of the death‐domain kinase RIP in tumour‐necrosis‐factor‐induced activation of mitogen‐activated protein kinases. EMBO Reports, 4(6), 623–627. Portico.

Authors 3
  1. Anne Devin (first)
  2. Yong Lin (additional)
  3. Zheng‐gang Liu (additional)
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Dates
Type When
Created 22 years, 3 months ago (May 16, 2003, 9:32 a.m.)
Deposited 1 year, 8 months ago (Dec. 18, 2023, 3:56 p.m.)
Indexed 3 weeks, 1 day ago (Aug. 6, 2025, 8:14 a.m.)
Issued 22 years, 3 months ago (May 16, 2003)
Published 22 years, 3 months ago (May 16, 2003)
Published Online 22 years, 3 months ago (May 16, 2003)
Published Print 22 years, 2 months ago (June 1, 2003)
Funders 0

None

@article{Devin_2003, title={The role of the death‐domain kinase RIP in tumour‐necrosis‐factor‐induced activation of mitogen‐activated protein kinases}, volume={4}, ISSN={1469-3178}, url={http://dx.doi.org/10.1038/sj.embor.embor854}, DOI={10.1038/sj.embor.embor854}, number={6}, journal={EMBO reports}, publisher={Springer Science and Business Media LLC}, author={Devin, Anne and Lin, Yong and Liu, Zheng‐gang}, year={2003}, month=may, pages={623–627} }