Cell intrinsic role of NF-κB-inducing kinase in regulating T cell-mediated immune and autoimmune responses

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作者
Yanchuan Li
Hui Wang
Xiaofei Zhou
Xiaoping Xie
Xiang Chen
Zuliang Jie
Qiang Zou
Hongbo Hu
Lele Zhu
Xuhong Cheng
Hans D Brightbill
Lawren C. Wu
Linfang Wang
Shao-Cong Sun
机构
[1] National Laboratory of Medical Molecular Biology,Department of Biochemistry and Molecular Biology
[2] Institute of Basic Medical Sciences,Department of Immunology
[3] Chinese Academy of Medical Sciences,Department of Immunology
[4] Peking Union Medical College,undefined
[5] Tsinghua University,undefined
[6] The University of Texas MD Anderson Cancer Center,undefined
[7] 7455 Fannin Street,undefined
[8] Box 902,undefined
[9] The University of Texas Graduate School of Biomedical Sciences,undefined
[10] State Key Laboratory of Biotherapy,undefined
[11] West China Hospital,undefined
[12] Si-Chuan University and Collaborative Innovation Center for Biotherapy,undefined
[13] Genentech Inc.,undefined
[14] Present address: Department of Oncology,undefined
[15] Amgen Inc.,undefined
[16] South San Francisco,undefined
[17] CA.,undefined
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摘要
NF-κB inducing kinase (NIK) is a central component of the noncanonical NF-κB signaling pathway. Although NIK has been extensively studied for its function in the regulation of lymphoid organ development and B-cell maturation, the role of NIK in regulating T cell functions remains unclear and controversial. Using T cell-conditional NIK knockout mice, we here demonstrate that although NIK is dispensable for thymocyte development, it has a cell-intrinsic role in regulating the homeostasis and function of peripheral T cells. T cell-specific NIK ablation reduced the frequency of effector/memory-like T cells and impaired T cell responses to bacterial infection. The T cell-conditional NIK knockout mice were also defective in generation of inflammatory T cells and refractory to the induction of a T cell-dependent autoimmune disease, experimental autoimmune encephalomyelitis. Our data suggest a crucial role for NIK in mediating the generation of effector T cells and their recall responses to antigens. Together, these findings establish NIK as a cell-intrinsic mediator of T cell functions in both immune and autoimmune responses.
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