Activation of SAPK/JNK by TNF receptor 1 through a noncytotoxic TRAF2-dependent pathway

被引:403
作者
Natoli, G
Costanzo, A
Ianni, A
Templeton, DJ
Woodgett, JR
Balsano, C
Levrero, M
机构
[1] POLICLIN UMBERTO 1,IST CLIN MED 1,I-00161 ROME,ITALY
[2] CASE WESTERN RESERVE UNIV,SCH MED,CLEVELAND,OH 44106
[3] PRINCESS MARGARET HOSP,ONTARIO CANC INST,TORONTO,ON M5G 2M9,CANADA
[4] UNIV AQUILA,DEPT MED INTERNA,I-67100 LAQUILA,ITALY
关键词
D O I
10.1126/science.275.5297.200
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interaction oi the p55 tumor necrosis factor receptor 1 (TNF-R1)-associated signal transducer TRADD with FADD signals apoptosis, whereas the TNF receptor-associated factor 2 protein (TRAF2) is required for activation of the nuclear transcription factor nuclear factor kappa B. TNF-induced activation of the stress-activated protein kinase (SAPK) was shown to occur through a noncytotoxic TRAF2-dependent pathway. TRAF2 was both sufficient and necessary for activation of SAPK by TNF-R1; conversely, expression of a dominant-negative FADD mutant, which blocks apoptosis, did not interfere with SAPK activation. Therefore, SAPK activation occurs through a pathway that is not required for TNF-R1-induced apoptosis.
引用
收藏
页码:200 / 203
页数:4
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