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

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 controv...

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Detalles Bibliográficos
Autores principales: Li, Yanchuan, Wang, Hui, Zhou, Xiaofei, Xie, Xiaoping, Chen, Xiang, Jie, Zuliang, Zou, Qiang, Hu, Hongbo, Zhu, Lele, Cheng, Xuhong, Brightbill, Hans D, Wu, Lawren C., Wang, Linfang, Sun, Shao-Cong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766435/
https://www.ncbi.nlm.nih.gov/pubmed/26912039
http://dx.doi.org/10.1038/srep22115
Descripción
Sumario: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.