Becker C G, Harpel P C
J Exp Med. 1976 Jul 1;144(1):1-9. doi: 10.1084/jem.144.1.1.
alpha2-Macroglobulin (alpha2M) has been identified on the luminal surface of endothelial cells in sections of normal human arteries, veins, and lymphatics by the indirect immunofluorescent technique. The specificity of the immunofluorescent reaction was confirmed by immunoabsorption studies. Prior absorption of the anti-alpha2M antiserum by purified alpha2M at equivalence completely inhibited endothelial surface as well as hepatic parenchymal cell staining. Endothelial cells in blood vessels were not stained when sections were treated with rabbit antisera toward alpha1-antitrypsin, antithrombin III, IgG, IgA, IgM, C3, or fibrinogen. The location of alpha2M at the surface of the vessel wall suggests that this protease inhibitor may protect the vascular endothelium from potentially injurious intravascular proteases.
通过间接免疫荧光技术,已在正常人动脉、静脉和淋巴管切片的内皮细胞腔面鉴定出α2-巨球蛋白(α2M)。免疫吸收研究证实了免疫荧光反应的特异性。用等量纯化的α2M预先吸收抗α2M抗血清可完全抑制内皮表面以及肝实质细胞的染色。当用针对α1-抗胰蛋白酶、抗凝血酶III、IgG、IgA、IgM、C3或纤维蛋白原的兔抗血清处理切片时,血管内皮细胞未被染色。α2M在血管壁表面的定位表明,这种蛋白酶抑制剂可能保护血管内皮免受潜在有害的血管内蛋白酶的损伤。