Chen Lu, Dong Wei, Zou Tingting, Ouyang Lu, He Guoqing, Liu Yingle, Qi Yipeng
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei, PR China.
FEBS Lett. 2008 Aug 20;582(19):2843-9. doi: 10.1016/j.febslet.2008.07.014. Epub 2008 Jul 15.
TRAF6 is an E3 ubiquitin ligase that transduces signals from members of the TLR/IL-1R family. Multiple molecules have been found to associate with TRAF6 and exert their functions in this pathway. Herein, by yeast two-hybrid screen using TRAF6 as bait, we identified PP4 as a potential TRAF6-interacting protein. PP4 physically interacted with TRAF6 and was recruited to TLR4 complex upon LPS stimulation. PP4 negatively regulated LPS-induced and TRAF6-mediated NF-kappaB activation by inhibiting the ubiquitination of TRAF6. LPS stimulation also induced the expression of PP4. Taken together, our findings suggest that PP4 is a negative feedback regulator of LPS/TLR4 pathway.
TRAF6是一种E3泛素连接酶,可转导来自TLR/IL-1R家族成员的信号。已发现多种分子与TRAF6相互作用并在该信号通路中发挥作用。在此,我们以TRAF6为诱饵,通过酵母双杂交筛选,鉴定出PP4是一种潜在的与TRAF6相互作用的蛋白。PP4与TRAF6发生物理相互作用,并在LPS刺激后被募集到TLR4复合物中。PP4通过抑制TRAF6的泛素化,对LPS诱导的以及TRAF6介导的NF-κB激活起负向调节作用。LPS刺激也可诱导PP4的表达。综上所述,我们的研究结果表明PP4是LPS/TLR4信号通路的负反馈调节因子。