Fischer E, Couturier C, Weiss L, Kazatchkine M D
INSERM U 28, Hôpital Broussais, Paris.
Nephrologie. 1991;12(4):169-78.
Most of the biological effects derived from complement activation depends on interactions between cleavage fragments of complement components and cells bearing specific receptors. This review overviews structure and function of receptors for C3 cleavage fragments. Genes encoding for CR1, CR2 and CR3 have been cloned and they code for integral transmembrane glycoproteins which function as cellular receptors for human C3b, C3dg/C3d and C3bi fragments respectively. These receptors have a wide cellular distribution and participate in transport of immune complexes, phagocytosis and regulation of immune response. Alterations of expression of these molecules are observed in pathology.
补体激活产生的大多数生物学效应取决于补体成分的裂解片段与带有特定受体的细胞之间的相互作用。本综述概述了C3裂解片段受体的结构和功能。编码CR1、CR2和CR3的基因已被克隆,它们分别编码完整的跨膜糖蛋白,作为人C3b、C3dg/C3d和C3bi片段的细胞受体。这些受体具有广泛的细胞分布,并参与免疫复合物的转运、吞噬作用和免疫反应的调节。在病理学中可观察到这些分子表达的改变。