Kelvin D J, Michiel D F, Johnston J A, Lloyd A R, Sprenger H, Oppenheim J J, Wang J M
Laboratory of Immunoregulation, Frederick Cancer Research and Development Center, Maryland 21702.
J Leukoc Biol. 1993 Dec;54(6):604-12. doi: 10.1002/jlb.54.6.604.
Chemokines are pro-inflammatory molecules with a diverse array of biological and biochemical functions. These molecules induce the migration of a number of leukocyte subsets including monocytes, neutrophils, and T-cells. The recent cloning of the IL-8, GRO, and MIP-1 alpha chemokine receptors revealed that these glycoproteins belong to the serpentine family of seven transmembrane G-protein-coupled receptors. Other members of this family include the chemotactic receptors for fMLP and C5a, indicating that a common pathway for eliciting the directional migration of leukocytes is probably transduced via G proteins. Ligand binding to chemokine receptors is complex, featured by multiple chemokines binding to a single receptor and multiple receptors binding a specific ligand. Future directions in this field appear to be focused on the cloning of novel receptors and the identification of ligands for orphaned receptors.
趋化因子是具有多种生物学和生化功能的促炎分子。这些分子可诱导包括单核细胞、中性粒细胞和T细胞在内的多种白细胞亚群迁移。最近对白细胞介素-8、生长调节致癌基因α(GRO)和巨噬细胞炎症蛋白-1α(MIP-1α)趋化因子受体的克隆表明,这些糖蛋白属于七个跨膜G蛋白偶联受体的蛇形家族。该家族的其他成员包括fMLP和C5a的趋化受体,这表明引发白细胞定向迁移的共同途径可能是通过G蛋白转导的。趋化因子受体与配体的结合很复杂,其特点是多种趋化因子与单个受体结合以及多种受体与特定配体结合。该领域未来的研究方向似乎集中在新型受体的克隆以及孤儿受体配体的鉴定上。