Johnston Brent, Butcher Eugene C
Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305-5324, USA.
Semin Immunol. 2002 Apr;14(2):83-92. doi: 10.1006/smim.2001.0345.
Leukocyte subsets are recruited from the blood to lymphoid and non-lymphoid tissues via a multi-step process that involves distinct adhesive and activation steps. Chemokines, a family of chemotactic cytokines that signal through G-protein-coupled receptors, play critical roles in regulating the leukocyte recruitment cascade. Chemokines can be transported and immobilized on the surface of vascular endothelial cells, where they activate leukocyte subsets expressing specific receptors. Activation signals induce firm adhesion of rolling leukocytes by rapidly upregulating integrin affinity and/or avidity. Chemokines can also direct migration of adherent cells across the endothelium, and control segregation of cells into specific microenvironments within tissues. The regulated expression of chemokines and their receptors is a critical determinant for homing of specialized lymphocyte subsets, and controls both tissue and inflammation-specific immune processes.
白细胞亚群通过一个多步骤过程从血液中募集到淋巴组织和非淋巴组织,该过程涉及不同的黏附与激活步骤。趋化因子是一类通过G蛋白偶联受体发出信号的趋化性细胞因子,在调节白细胞募集级联反应中发挥关键作用。趋化因子可被转运并固定在血管内皮细胞表面,在那里它们激活表达特定受体的白细胞亚群。激活信号通过快速上调整合素亲和力和/或亲合力诱导滚动白细胞牢固黏附。趋化因子还可引导黏附细胞穿过内皮迁移,并控制细胞在组织内特定微环境中的分隔。趋化因子及其受体的调控表达是特定淋巴细胞亚群归巢的关键决定因素,并控制组织特异性和炎症特异性免疫过程。