Purification and characterization of a complex from placental syncytiotrophoblast microvillous membranes which inhibits the proliferation of human umbilical vein endothelial cells

被引:26
作者
Kertesz, Z [1 ]
Hurst, G
Ward, M
Willis, AC
Caro, H
Linton, EA
Sargent, IL
Redman, CWG
机构
[1] Univ Oxford, Nuffield Dept Obstet & Gynaecol, Oxford OX3 9DU, England
[2] Glaxo Wellcome Res & Dev Ltd, Med Ctr, Biomol Struct Unit, Stevenage SG1 2NY, Herts, England
[3] Univ Oxford, Dept Biochem, MRC, Immunochem Unit, Oxford OX1 3QU, England
[4] UCL, Sch Med, Dept Mol Pathol, London W1P 6DB, England
基金
英国惠康基金;
关键词
D O I
10.1053/plac.1998.0351
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The signs of pre-eclampsia are thought to arise from maternal endothelial dysfunction caused by circulating factors of placental origin. Syncytiotrophoblast microvillous membranes (STBM) cause endothelial disruption and inhibit proliferation in vitro. Significantly increased amounts of STBM can be detected in blood from pre-eclamptic women and could contribute to endothelial dysfunction in vivo. This study purified a complex from STEM which inhibits the proliferation of cultured human endothelial cells. Integral membrane proteins were solubilized with sucrose monolaurate. Anion exchange chromatography yielded two peaks of anti-proliferative activity. Only the second peak was specific to STEM and was subjected to further separation by Sephacryl S-200 gel filtration chromatography (GFC). A single peak of specific activity eluted close to the void volume, at a position unaltered by added denaturing agents, guanidium chloride or urea. On Sephacryl S-300 GFC, two peaks were obtained of 410 and 820 kDa, with similar anti-proliferative activity and protein components (by SDS-polyacrylamide gel electrophoresis). The major protein bands were as integrins alpha(5) and alpha(v), dipeptidyl peptidase IV, alpha-actinin, transferrin, transferrin receptor, placental alkaline phosphatase and monoamine oxidase A. (C) 1999 W. B. Saunders Company Ltd.
引用
收藏
页码:71 / 79
页数:9
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