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磷酸酶PTPN4通过使TRAM去磷酸化来优先抑制依赖TRIF的TLR4信号通路。

Phosphatase PTPN4 preferentially inhibits TRIF-dependent TLR4 pathway by dephosphorylating TRAM.

作者信息

Huai Wanwan, Song Hui, Wang Lijuan, Li Bingqing, Zhao Jing, Han Lihui, Gao Chengjiang, Jiang Guosheng, Zhang Lining, Zhao Wei

机构信息

Department of Immunology, Shandong University School of Medicine, Jinan, Shandong 250012, China;

Pathology Tissue Bank, Qilu Hospital, Shandong University, Jinan, Shandong 250012, China; and.

出版信息

J Immunol. 2015 May 1;194(9):4458-65. doi: 10.4049/jimmunol.1402183. Epub 2015 Mar 30.

Abstract

TLR4 recruits TRIF-related adaptor molecule (TRAM, also known as TICAM2) as a sorting adaptor to facilitate the interaction between TLR4 and TRIF and then initiate TRIF-dependent IRF3 activation. However, the mechanisms by which TRAM links downstream molecules are not fully elucidated. In this study, we show that TRAM undergoes tyrosine phosphorylation upon TLR4 activation and that is required for TLR4-induced IRF3 activation. Protein tyrosine phosphatase nonreceptor type 4 (PTPN4), a protein tyrosine phosphatase, inhibits tyrosine phosphorylation and subsequent cytoplasm translocation of TRAM, resulting in the disturbance of TRAM-TRIF interaction. Consequently, PTPN4 specifically inhibits TRIF-dependent IRF3 activation and IFN-β production in TLR4 pathway. Therefore, our results provide new insight into the TLR4 pathway and identify PTPN4 as a specific inhibitor of TRIF-dependent TLR4 pathway. Targeting PTPN4 would be beneficial for the development of new strategy to control TLR4-associated diseases without unwanted side effects.

摘要

Toll样受体4(TLR4)招募TRIF相关衔接分子(TRAM,也称为TICAM2)作为分选衔接子,以促进TLR4与TRIF之间的相互作用,进而启动依赖TRIF的IRF3激活。然而,TRAM连接下游分子的机制尚未完全阐明。在本研究中,我们发现TRAM在TLR4激活后发生酪氨酸磷酸化,这是TLR4诱导IRF3激活所必需的。蛋白酪氨酸磷酸酶非受体4型(PTPN4)作为一种蛋白酪氨酸磷酸酶,可抑制TRAM的酪氨酸磷酸化及其随后的细胞质转位,从而导致TRAM与TRIF相互作用的紊乱。因此,PTPN4特异性抑制TLR4信号通路中依赖TRIF的IRF3激活和IFN-β产生。所以,我们的研究结果为TLR4信号通路提供了新的见解,并确定PTPN4是依赖TRIF的TLR4信号通路的特异性抑制剂。靶向PTPN4将有助于开发控制TLR4相关疾病的新策略,且不会产生不良副作用。

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