Mondino B J, Sundar-Raj C V, Brady K J
Arch Ophthalmol. 1982 Mar;100(3):478-80. doi: 10.1001/archopht.1982.01030030480022.
Corneal fibroblasts were studied to determine if they have the ability to synthesize and secrete complement components in tissue culture. Culture media were assayed for functional complement activity of C1, C4, C2, C3, C5, C6, and C7 with the use of 50% hemolysis of sensitized sheep RBCs. Only C1 showed a progressive increase in hemolytic activity at days 3, 5, 7, 9, and 11 of tissue culture. This increase in hemolytic C1 could be reversibly inhibited by cycloheximide, an inhibitor of protein synthesis. Corneal fibroblasts may be a potential source of C1 in the cornea.
研究角膜成纤维细胞,以确定它们在组织培养中是否具有合成和分泌补体成分的能力。使用致敏绵羊红细胞50%溶血法检测培养基中C1、C4、C2、C3、C5、C6和C7的功能性补体活性。在组织培养的第3、5、7、9和11天,只有C1的溶血活性呈逐渐增加。溶血C1的这种增加可被蛋白质合成抑制剂环己酰亚胺可逆性抑制。角膜成纤维细胞可能是角膜中C1的潜在来源。