HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS SYNTHESIZE FUNCTIONAL C3, C5, C6, C8 AND C9 INVITRO

被引:37
作者
JOHNSON, E
HETLAND, G
机构
[1] ULLEVAL HOSP,INST EXPT MED RES,N-0407 OSLO 4,NORWAY
[2] ULLEVAL HOSP,BLOOD BANK,N-0407 OSLO 4,NORWAY
[3] ULLEVAL HOSP,DEPT IMMUNOL,N-0407 OSLO 4,NORWAY
关键词
D O I
10.1111/j.1365-3083.1991.tb02539.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human endothelial cells (EC), cultured serum-free, synthesize de novo protein which increasingly bind to agarose beads (an alternative pathway activator), until a plateau phase is reached after 24-48 h. EC synthesize functional C3, C5, C6, C8 and C9, which were detected on co-cultured agarose beads, using relevant polyclonal anti-complement antibodies. Two monoclonal anti-C9 neoepitope antibodies (aE11, poly C9-MA) bound to the co-cultured beads, showing that the terminal complement complex (TCC) (C5b-9) was assembled on the beads. This also suggests that C7 is synthesized. There seems to be a positive correlation between the amount of agarose-bound labelled protein and agarose-bound complement. The results indicate that EC produce and secrete the components for the functional alternative and terminal pathways of complement.
引用
收藏
页码:667 / 671
页数:5
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