Laboratory of Autoimmunity and Tolerance, National Centre for Cell Science, Pune, India.
Front Immunol. 2020 Oct 2;11:536326. doi: 10.3389/fimmu.2020.536326. eCollection 2020.
Chemokine receptor CCR9 is a G protein-coupled receptor and expressed on several types of immune cells, including dendritic cells (DCs), CD4 T cells, and B cells. CCR9 drives the migration of immune cells to gradients of its cognate ligand CCL25. The chemokine CCL25 is mostly produced by gut and thymic epithelial cells. Gut- and thymic-homing DCs are known to express CCR9, and these cells are predominantly localized in the gut lining and thymus. CCR9 DCs are implicated in regulating inflammation, food allergy, alloimmunity, and autoimmunity. Differential interaction of CCR9 DCs with lymphoid and myeloid cells in the thymus, secondary lymphoid tissues, and mucosal sites offer crucial insights to immune regulation. In this review, we examine the phenotypes, distributions, and interactions of CCR9 DCs with other immune cells, elucidating their functions and role in inflammation and autoimmunity.
趋化因子受体 CCR9 是一种 G 蛋白偶联受体,表达于多种免疫细胞上,包括树突状细胞(DC)、CD4 T 细胞和 B 细胞。CCR9 驱动免疫细胞向其同源配体 CCL25 的浓度梯度迁移。趋化因子 CCL25 主要由肠道和胸腺上皮细胞产生。已知归巢于肠道和胸腺的 DC 表达 CCR9,这些细胞主要定位于肠道衬里和胸腺。CCR9 DC 参与调节炎症、食物过敏、同种免疫和自身免疫。CCR9 DC 与胸腺、次级淋巴组织和黏膜部位的淋巴样和髓样细胞的差异相互作用为免疫调节提供了重要的见解。在这篇综述中,我们检查了 CCR9 DC 与其他免疫细胞的表型、分布和相互作用,阐明了它们在炎症和自身免疫中的功能和作用。