Division of Biosignal Regulation, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe 650-0047, Japan.
Division of Molecular and Cellular Signaling, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
Proc Natl Acad Sci U S A. 2023 Aug 15;120(33):e2304943120. doi: 10.1073/pnas.2304943120. Epub 2023 Aug 7.
Conventional dendritic cells (cDCs) are required for peripheral T cell homeostasis in lymphoid organs, but the molecular mechanism underlying this requirement has remained unclear. We here show that T cell-specific CD47-deficient () mice have a markedly reduced number of T cells in peripheral tissues. Direct interaction of CD47-deficient T cells with cDCs resulted in activation of the latter cells, which in turn induced necroptosis of the former cells. The deficiency and cell death of T cells in mice required expression of its receptor signal regulatory protein α on cDCs. The development of CD4 T helper cell-dependent contact hypersensitivity and inhibition of tumor growth by cytotoxic CD8 T cells were both markedly impaired in mice. CD47 on T cells thus likely prevents their necroptotic cell death initiated by cDCs and thereby promotes T cell survival and function.
传统树突状细胞(cDCs)是外周 T 细胞在淋巴器官中维持稳态所必需的,但这一需求的分子机制仍不清楚。我们在这里表明,T 细胞特异性 CD47 缺陷()小鼠在外周组织中的 T 细胞数量明显减少。CD47 缺陷 T 细胞与 cDCs 的直接相互作用导致后者细胞的激活,进而诱导前者细胞的坏死性凋亡。cDCs 上信号调节蛋白α受体的表达是 小鼠中 T 细胞缺陷和细胞死亡所必需的。在 小鼠中,CD4 T 辅助细胞依赖性接触超敏反应和细胞毒性 CD8 T 细胞抑制肿瘤生长的能力均明显受损。因此,T 细胞上的 CD47 可能防止了由 cDCs 引发的 T 细胞坏死性凋亡,从而促进了 T 细胞的存活和功能。