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A miR-155-Peli1-c-Rel pathway controls the generation and function of T follicular helper cells.
Liu, Wen-Hsien; Kang, Seung Goo; Huang, Zhe; Wu, Cheng-Jang; Jin, Hyun Yong; Maine, Christian J; Liu, Yi; Shepherd, Jovan; Sabouri-Ghomi, Mohsen; Gonzalez-Martin, Alicia; Xu, Shunbin; Hoffmann, Alexander; Zheng, Ye; Lu, Li-Fan; Xiao, Nengming; Fu, Guo; Xiao, Changchun.
Afiliação
  • Liu WH; State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China cxiao@scripps.edu whliu@xmu.edu.cn guofu@xmu.edu.cn.
  • Kang SG; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037 Division of Biomedical Convergence/Institute of Bioscience and Biotechnology, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.
  • Huang Z; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
  • Wu CJ; Division of Biological Sciences, Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093.
  • Jin HY; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
  • Maine CJ; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
  • Liu Y; Department of Microbiology, Immunology, and Molecular Genetics, Institute for Quantitative and Computational Biosciences, University of California, Los Angeles, Los Angeles, CA 90095.
  • Shepherd J; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
  • Sabouri-Ghomi M; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
  • Gonzalez-Martin A; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
  • Xu S; Department of Ophthalmology/Kresge Eye Institute, School of Medicine, Wayne State University, Detroit, MI 48202 Department of Anatomy and Cell Biology, School of Medicine, Wayne State University, Detroit, MI 48202.
  • Hoffmann A; Department of Microbiology, Immunology, and Molecular Genetics, Institute for Quantitative and Computational Biosciences, University of California, Los Angeles, Los Angeles, CA 90095.
  • Zheng Y; Nomis Foundation Laboratories for Immunobiology and Microbial Pathogenesis, Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Lu LF; Division of Biological Sciences, Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093.
  • Xiao N; State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China.
  • Fu G; State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China cxiao@scripps.edu whliu@xmu.edu.cn guofu@xmu.edu.cn.
  • Xiao C; State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037 cxiao@scripps.edu whliu@xmu.edu.cn guofu@
J Exp Med ; 213(9): 1901-19, 2016 08 22.
Article em En | MEDLINE | ID: mdl-27481129
ABSTRACT
MicroRNA (miRNA) deficiency impairs the generation of T follicular helper (Tfh) cells, but the contribution of individual miRNAs to this phenotype remains poorly understood. In this study, we performed deep sequencing analysis of miRNAs expressed in Tfh cells and identified a five-miRNA signature. Analyses of mutant mice deficient of these miRNAs revealed that miR-22 and miR-183/96/182 are dispensable, but miR-155 is essential for the generation and function of Tfh cells. miR-155 deficiency led to decreased proliferation specifically at the late stage of Tfh cell differentiation and reduced CD40 ligand (CD40L) expression on antigen-specific CD4(+) T cells. Mechanistically, miR-155 repressed the expression of Peli1, a ubiquitin ligase that promotes the degradation of the NF-κB family transcription factor c-Rel, which controls cellular proliferation and CD40L expression. Therefore, our study identifies a novel miR-155-Peli1-c-Rel pathway that specifically regulates Tfh cell generation and function.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Transdução de Sinais / Linfócitos T Auxiliares-Indutores / Proteínas Proto-Oncogênicas c-rel / MicroRNAs / Ubiquitina-Proteína Ligases Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Transdução de Sinais / Linfócitos T Auxiliares-Indutores / Proteínas Proto-Oncogênicas c-rel / MicroRNAs / Ubiquitina-Proteína Ligases Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article