Macrophage inhibitory cytokine-1 in gestational tissues and maternal serum in normal and pre-eclamptic pregnancy

被引:72
作者
Marjono, AB
Brown, DA
Horton, KE
Wallace, EM
Breit, SN
Manuelpillai, U
机构
[1] Monash Univ, Dept Obstet & Gynaecol, Med Ctr, Ctr Womens Hlth Res, Clayton, Vic 3168, Australia
[2] Univ New S Wales, Sydney, NSW, Australia
[3] St Vincents Hosp, Ctr Immunol, Sydney, NSW 2010, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1053/plac.2002.0881
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
DMacrophage inhibitory cytokine-1 (MIC-1), a divergent member of transforming growth factor-beta superfamily, has been recently shown to be produced by the human placenta with detectable levels in maternal serum. In this study, using immunohistochemistry, we have localized MIC-1 in placenta, decidua and foetal membranes across pregnancy and, using an enzyme-linked immunoassay, measured MIC-1 in maternal serum in normal pregnancy, in association with labour and pre-eclampsia. In the placenta MIC-1 was principally localized to the syncytiotrophoblast while in the foetal membranes MIC-1 was present in the amniotic epithelium, chorionic trophoblasts and adherent decidual cells. There were no differences in MIC-1 staining distribution or intensity in the placentae between women in labour and not in labour, or between healthy and pre-eclamptic pregnancies. MIC-1 staining in the foetal membranes was slightly stronger after a labour and delivery compared to those delivered by elective Caesarean section. MIC-1 levels in the maternal serum increased with advancing gestation but there were no significant differences in maternal serum levels associated with either labour or pre-eclampsia. These observations would be consistent with MIC-1 having roles at the maternal-foetal interface, perhaps in the establishment and/or maintenance of pregnancy. Our data argue against MICA having a significant role in the regulation of labour or in the pathophysiology of pre-eclampsia. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
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页码:100 / 106
页数:7
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