Sphingosine kinase interacts with TRAF2 and dissects tumor necrosis factor-α signaling

被引:256
作者
Xia, P
Wang, LJ
Moretti, PAB
Albanese, N
Chai, FG
Pitson, SM
D'Andrea, RJ
Gamble, JR
Vadas, MA
机构
[1] Inst Med & Vet Sci, Hanson Inst, Div Human Immunol, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Adelaide, SA 5000, Australia
关键词
D O I
10.1074/jbc.M111423200
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-alpha (TNF) receptor-associated factor 2 (TRAF2) is one of the major mediators of TNF receptor superfamily transducing TNF signaling to various functional targets, including activation of NF-kappaB, JNK, and antiapoptosis. We investigated how TRAF2 mediates differentially the distinct downstream signals. We now report a novel mechanism of TRAF2-mediated signal transduction revealed by an association of TRAF2 with sphingosine kinase (SphK), a lipid kinase that is responsible for the production of sphingosine 1-phosphate. We identified a TRAF2-binding motif of SphK that mediated the interaction between TRAF2 and SphK resulting in the activation of the enzyme, which in turn is required for TRAF2-mediated activation of NF-kappaB but not JNK In addition, by using a kinase inactive dominant-negative SphK and a mutant SphK that lacks TRAF2-binding motif we show that the interaction of TRAF2 with SphK and subsequent activation of SphK are critical for prevention of apoptosis during TNF stimulation. These findings show a role for SphK in the signal transduction by TRAF2 specifically leading to activation of NF-kappaB and antiapoptosis.
引用
收藏
页码:7996 / 8003
页数:8
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