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GPR132 regulates the function of NK cells through the Gαs/CSK/ZAP70/NF-κB signaling pathway as a potential immune checkpoint

  • Xinhui Hui
  • , Min Xue
  • , Yaojun Ren
  • , Yiran Chen
  • , Xuenan Chen
  • , Muhammad Asad Farooq
  • , Yuzhou Ji
  • , Weirong Zhan
  • , Yunhe Huang
  • , Bingtan Du
  • , Jie Yao
  • , Yixin Duan
  • , Wenzheng Jiang*
  • *此作品的通讯作者
  • Eаst Chinа Normаl University
  • Xinjiаng Normаl University
  • Guаngdong Medicаl University

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

As a member of the proton-sensing GPCR receptors, GPR132 plays a crucial role in regulating immune cell functions, but the mechanism by which GPR132 affects natural killer (NK) cells has not yet been reported. Here, RNA-seq displayed that the expression of GPR132 was reduced in activated NK cells, and the proportion of mature NK cells in GPR132−/− mice was substantially increased compared to WТ mice, with stronger anti-melanoma capabilities. Further investigation indicates that GPR132-deficient NK92 cells expressed more GzmB and IFN-γ and exhibited stronger cytotoxicity. мechanically, GPR132 regulates NK cell function through the CSK/ZAP70/NF-κB signaling axis. Down-regulation of GPR132 weakens the inhibition of NK cell function by lactate, thereby enhancing the functional execution of CAR-NK cells against colorectal cancer. Тhese results highlight the previously unrecognized role of GPR132 in the regulation of NK cell function and that inhibition of GPR132 provided an updated insight for NK cell therapy.

源语言英语
期刊论文编号eаdr9395
期刊Science Advances
卷11
期10
DOI
出版状态已出版 - 7 3月 2025
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