Chemokine-chemokine receptor network in immune cell trafficking.

Chang H Kim
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引用次数: 93

Abstract

Chemokines play critical roles in leukocyte trafficking in normal and inflammatory conditions. The primary roles of chemokines are to activate integrins for leukocyte adherence on endothelial cells and to induce chemotaxis of leukocytes in tissue microenvironments. Specificity in leukocyte migration is regulated at multiple levels. First, it is achieved through differential tissue expression of chemokines and adhesion molecules. Second, it is achieved by limited and differential expression of chemokine receptors by leukocyte subsets. Third, combinatorial expression of multiple chemokine receptors and adhesion molecules makes leukocyte migration more specific. Homing of leukocytes into various tissue sites (e.g. inflamed skin, small intestine, mucosal tissues, T cell areas vs. B cell follicles) requires different chemokines and chemokine receptors. Furthermore, distinct immune responses and diseases (e.g. Th1 vs. Th2 responses) involve different sets of chemokines and leukocyte subsets. This review examines the recent advances in research on chemokines and chemokine receptors in tissue-specific migration of immune cells, and discusses potential targets of intervention in chemokine-mediated leukocyte migration in normal and diseased conditions.

免疫细胞运输中的趋化因子-趋化因子受体网络。
趋化因子在正常和炎症条件下的白细胞运输中发挥关键作用。趋化因子的主要作用是激活整合素,使白细胞粘附在内皮细胞上,并在组织微环境中诱导白细胞趋化。白细胞迁移的特异性在多个水平上受到调节。首先,它是通过趋化因子和粘附分子的组织差异表达实现的。其次,它是通过白细胞亚群有限和差异的趋化因子受体表达来实现的。第三,多种趋化因子受体和粘附分子的组合表达使白细胞迁移更具特异性。白细胞归巢到不同的组织部位(如发炎的皮肤、小肠、粘膜组织、T细胞区与B细胞滤泡)需要不同的趋化因子和趋化因子受体。此外,不同的免疫反应和疾病(例如Th1与Th2反应)涉及不同的趋化因子和白细胞亚群。本文综述了近年来趋化因子和趋化因子受体在免疫细胞组织特异性迁移中的研究进展,并讨论了在正常和病变情况下,干预趋化因子介导的白细胞迁移的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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