School Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
J Biol Chem. 2012 Mar 30;287(14):11002-10. doi: 10.1074/jbc.M111.328187. Epub 2012 Jan 19.
The Toll-like receptor (TLR)/IL-1 receptor (IL-1R) signaling pathway is essential for innate immune responses and immune homeostasis. Lys-63-polyubiquitinated TRAF6 mediates its downstream signaling activation. In a gain-of-expression screen of 66 different deubiquitinating enzymes, we identified USP4 as a potent negative regulator of TLR/IL-1R signaling and TRAF6-interacting protein. USP4 deubiquitinates TRAF6 and thereby prevents the activation of NF-κB and AP-1 transcription factors and subsequent proinflammatory responses. LPS-treated usp4-depleted zebrafish larvae expressed higher levels of proinflammatory cytokines and were more susceptible to endotoxic challenge. Taken together, our results demonstrate that USP4 plays an essential role in negative regulation of the TLR/IL-1R signaling-mediated innate immune response.
Toll 样受体 (TLR)/IL-1 受体 (IL-1R) 信号通路对于先天免疫反应和免疫稳态至关重要。赖氨酸 63 多聚泛素化 TRAF6 介导其下游信号激活。在对 66 种不同去泛素化酶的表达增加筛选中,我们发现 USP4 是 TLR/IL-1R 信号和 TRAF6 相互作用蛋白的有效负调控因子。USP4 去泛素化 TRAF6,从而防止 NF-κB 和 AP-1 转录因子的激活以及随后的促炎反应。用 LPS 处理的usp4 耗尽的斑马鱼幼虫表达更高水平的促炎细胞因子,并且更容易受到内毒素挑战。总之,我们的结果表明 USP4 在 TLR/IL-1R 信号介导的先天免疫反应的负调控中发挥重要作用。