Phosphatase PTPN4 Preferentially Inhibits TRIF-Dependent TLR4 Pathway by Dephosphorylating TRAM

被引:28
|
作者
Huai, Wanwan [1 ]
Song, Hui [1 ]
Wang, Lijuan [2 ]
Li, Bingqing [3 ]
Zhao, Jing [1 ]
Han, Lihui [1 ]
Gao, Chengjiang [1 ]
Jiang, Guosheng [3 ]
Zhang, Lining [1 ]
Zhao, Wei [1 ]
机构
[1] Shandong Univ, Sch Med, Dept Immunol, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Qilu Hosp, Pathol Tissue Bank, Jinan 250012, Shandong, Peoples R China
[3] Shandong Acad Med Sci, Inst Basic Med, Jinan 250062, Shandong, Peoples R China
来源
JOURNAL OF IMMUNOLOGY | 2015年 / 194卷 / 09期
基金
中国国家自然科学基金;
关键词
PROTEIN-TYROSINE PHOSPHATASES; TOLL-LIKE RECEPTORS; NF-KAPPA-B; I-INTERFERON; SIGNAL-TRANSDUCTION; ADAPTER MOLECULE; PROINFLAMMATORY CYTOKINE; PROTEASOMAL DEGRADATION; INNATE IMMUNITY; RIG-I;
D O I
10.4049/jimmunol.1402183
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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-beta 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.
引用
收藏
页码:4458 / 4465
页数:8
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