| First Author | Wong WW | Year | 2010 |
| Journal | Cell Death Differ | Volume | 17 |
| Issue | 3 | Pages | 482-7 |
| PubMed ID | 19927158 | Mgi Jnum | J:169430 |
| Mgi Id | MGI:4940962 | Doi | 10.1038/cdd.2009.178 |
| Citation | Wong WW, et al. (2010) RIPK1 is not essential for TNFR1-induced activation of NF-kappaB. Cell Death Differ 17(3):482-7 |
| abstractText | On TNF binding, receptor-interacting protein kinase 1 (RIPK1) is recruited to the cytoplasmic domain of TNFR1, at which it becomes ubiquitylated and serves as a platform for recruitment and activation of NEMO/IKK1/IKK2 and TAK1/TAB2. RIPK1 is commonly thought to be required for the activation of canonical NF-kappaB and for inhibition TNFR1-induced apoptosis. RIPK1 has, however, also been reported to be essential for TNFR1-induced apoptosis when cIAPs are depleted. To determine the role of RIPK1 in TNF/IAP antagonist-induced death, we compared wild type (WT) and RIPK1(-/-) mouse embryonic fibroblasts (MEFs) treated with these compounds. On being treated with TNF plus IAP antagonist, RIPK1(-/-) MEFs survived, unlike WT MEFs, demonstrating a killing activity of RIPK1. Surprisingly, however, on being treated with TNF alone, RIPK1(-/-) MEFs activated canonical NF-kappaB and did not die. Furthermore, several cell types from E18 RIPK1(-/-) embryos seem to activate NF-kappaB in response to TNF. These data indicate that models proposing that RIPK1 is essential for TNFR1 to activate canonical NF-kappaB are incorrect. |
