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CD147 regulates the formation and function of immune synapses.
Xu, Yingming; Zhang, Kui; Miao, Jinlin; Guo, Na; Fu, Xianghui; Yang, Fengfan; Luo, Xing; Jia, Junfeng; Zheng, Zhaohui; Zhu, Ping.
Afiliação
  • Xu Y; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: xuyingming@fmmu.edu.cn.
  • Zhang K; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: zhk100@fmmu.edu.cn.
  • Miao J; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: miaojinlin@fmmu.edu.cn.
  • Guo N; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China; Department of Immunology, School of Basic Medicine, Xian Medical University, Xi'an, China. Electronic
  • Fu X; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: fuxianghui0225@126.com.
  • Yang F; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: yangfengfan6975@sina.cn.
  • Luo X; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: karalx@163.com.
  • Jia J; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: junfeng@fmmu.edu.cn.
  • Zheng Z; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: zhengzh@fmmu.edu.cn.
  • Zhu P; Department of Clinical Immunology, Xijing Hospital, and Department of Cell Biology of National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China. Electronic address: zhuping@fmmu.edu.cn.
Cell Immunol ; 401-402: 104845, 2024.
Article em En | MEDLINE | ID: mdl-38909549
ABSTRACT
CD147 is a T cell activation-associated molecule which is closely involved in the formation of the immune synapse (IS). However, the precise role of CD147 in T cell activation and IS formation remains unclear. In the present study, we demonstrated that CD147 translocated to the IS upon T cell activation and was primarily distributed in the peripheral super molecular cluster (p-SMAC). The knock down of CD147 expression in T cells, but not in B cells, impaired IS formation. CD147 participated in IS formation between T cells and different types of antigen-presenting cells (APCs), including macrophages and dendritic cells. Ligation of CD147 with its monoclonal antibody (mAb) HAb18 effectively inhibited T cell activation and IL-2 secretion. CD98, a critical molecule interacting with CD147, was distributed in IS in a CD147-dependent way. Phosphorylation levels of T cell receptor (TCR) related molecules, like ZAP-70, ERK, and cJun, were down-regulated by CD147 ligation, which is crucial for the interaction of CD147 and TCR signaling transduction. CD147 is indispensable for the formation of immune synapses and plays an important role in the regulation of its function.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ativação Linfocitária / Linfócitos T / Basigina / Sinapses Imunológicas Limite: Animals / Humans Idioma: En Revista: Cell Immunol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ativação Linfocitária / Linfócitos T / Basigina / Sinapses Imunológicas Limite: Animals / Humans Idioma: En Revista: Cell Immunol Ano de publicação: 2024 Tipo de documento: Article