Department of Infectious Diseases, St. Jude Childrens Research Hospital, Memphis, Tennessee 38105, USA.
Nat Rev Immunol. 2011 Jun 10;11(7):457-68. doi: 10.1038/nri2998.
Tumour necrosis factor receptor (TNFR)-associated factor (TRAF) proteins are essential components of signalling pathways activated by TNFR or Toll-like receptor (TLR) family members. Acting alone or in combination, the seven known TRAFs control many biological processes, including cytokine production and cell survival. The function of one TRAF in particular, TRAF3, remained elusive for many years. Recent work has revealed that TRAF3 is a highly versatile regulator that positively controls type I interferon production, but negatively regulates mitogen-activated protein kinase activation and alternative nuclear factor-κB signalling. In this Review, we discuss our current understanding of the role of TRAF3 in TNFR and TLR signalling pathways, and its role in disease.
肿瘤坏死因子受体(TNFR)相关因子(TRAF)蛋白是 TNFR 或 Toll 样受体(TLR)家族成员激活的信号通路的重要组成部分。这七种已知的 TRAFs 单独或组合作用,控制着许多生物学过程,包括细胞因子的产生和细胞存活。其中一个 TRAF 的功能,TRAF3,多年来一直难以捉摸。最近的研究表明,TRAF3 是一种高度通用的调节剂,它正向控制 I 型干扰素的产生,但负向调节丝裂原活化蛋白激酶的激活和替代核因子-κB 信号转导。在这篇综述中,我们讨论了我们目前对 TRAF3 在 TNFR 和 TLR 信号通路中的作用及其在疾病中的作用的理解。