Baggiolini M, Loetscher P, Moser B
Theodor-Kocher Institute, University of Bern, Switzerland.
Int J Immunopharmacol. 1995 Feb;17(2):103-8. doi: 10.1016/0192-0561(94)00088-6.
Two subfamilies of chemokines are distinguished depending on the arrangement of the first two of four conserved cysteines, which are either separated by one amino acid (CXC chemokines) or adjacent (CC chemokines). IL-8 and the other CXC chemokines act preferentially on neutrophils, while the CC chemokines (MCP-1, MCP-2, MCP-3, RANTES, MIP-1 alpha and MIP-1 beta) act on monocytes, but not neutrophils, and have additional activities toward basophil and eosinophil granulocytes, and T-lymphocytes. Several chemokine receptors have been identified, all of which belong to the seven-transmembrane-domain type and are coupled to G-proteins. The discovery of chemokines has provided the basis for the understanding of leukocyte recruitment and activation in inflammation and other disturbances of tissue homeostasis.
趋化因子可根据四个保守半胱氨酸中前两个的排列方式分为两个亚家族,它们要么被一个氨基酸隔开(CXC趋化因子),要么相邻(CC趋化因子)。白细胞介素-8和其他CXC趋化因子主要作用于中性粒细胞,而CC趋化因子(单核细胞趋化蛋白-1、单核细胞趋化蛋白-2、单核细胞趋化蛋白-3、调节激活正常T细胞表达和分泌因子、巨噬细胞炎性蛋白-1α和巨噬细胞炎性蛋白-1β)作用于单核细胞,而非中性粒细胞,并且对嗜碱性粒细胞、嗜酸性粒细胞和T淋巴细胞还有其他作用。已经鉴定出几种趋化因子受体,它们都属于七跨膜结构域类型,并与G蛋白偶联。趋化因子的发现为理解炎症及其他组织内环境稳定紊乱中白细胞的募集和激活提供了基础。