Critical roles of TRAF2 and TRAF5 in tumor necrosis factor-induced NF-κB activation and protection from cell death

被引:246
作者
Tada, K
Okazaki, T
Sakon, S
Kobarai, T
Kurosawa, K
Yamaoka, S
Hashimoto, H
Mak, TW
Yagita, H
Okumura, K
Yeh, WC
Nakano, H
机构
[1] Juntendo Univ, Sch Med, Dept Immunol, Bunkyo Ku, Tokyo 1138421, Japan
[2] Juntendo Univ, Sch Med, Dept Rheumatol & Internal Med, Bunkyo Ku, Tokyo 1138421, Japan
[3] Japan Sci & Technol Corp, PRESTO, Shibuya Ku, Tokyo 1510053, Japan
[4] CREST, Japan Sci & Techol Corp, Chiyoda Ku, Tokyo 1010062, Japan
[5] Tokyo Med & Dent Univ, Sch Med, Dept Microbiol, Bunkyo Ku, Tokyo 1138519, Japan
[6] Univ Toronto, Ontario Canc Inst, Amgen Inst, Toronto, ON M5G 2M9, Canada
[7] Univ Toronto, Ontario Canc Inst, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
关键词
D O I
10.1074/jbc.M104837200
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
Tumor necrosis factor (TNF) receptor-associated factors (TRAFs) were identified as signal transducers for the TNF receptor superfamily. However, the exact roles of TRAF2 and TRAF5 in TNF-induced NF-kappaB activation still remain controversial. To address this issue, we generated TRAF2 and TRAF5 double knockout (DKO) mice. TNF- but not interleukin-1-induced nuclear translocation of NF-kappaB was severely impaired in murine embryonic fibroblasts (MEFs) derived from DKO mice. Moreover, DKO MEFs were more susceptible to TNF-induced cytotoxicity than TRAF2 knockout MEFs. Collectively, these results indicate that both TRAF2 and TRAF5 are involved in TNF-induced NF-kappaB activation and protection from cell death.
引用
收藏
页码:36530 / 36534
页数:5
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