Expression of natural antimicrobials by human placenta and fetal membranes

被引:176
作者
King, A. E.
Paltoo, A.
Kelly, R. W.
Sallenave, J. -M.
Bocking, A. D.
Challis, J. R. G.
机构
[1] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Dept Obstet & Gynaecol, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Med, Toronto, ON M5S 1A8, Canada
[4] MRC, Ctr Reprod Biol, Human Reprod Sci Unit, Edinburgh EH16 4SB, Midlothian, Scotland
[5] Univ Edinburgh, Sch Med, MRC, Ctr Inflammat Res, Edinburgh EH8 9AG, Midlothian, Scotland
基金
加拿大健康研究院;
关键词
natural antimicrobials; placenta; fetal membranes; labour; infection;
D O I
10.1016/j.placenta.2006.01.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Preterm birth associated with infection is a major clinical problem. We hypothesized that this condition is associated with altered expression natural antimicrobial molecules ( beta-defensins (HBD), elafin). Therefore, we examined expression of these molecules and their regulation by proinflammatory cytokines in placentae and fetal membranes from term pregnancy. HBD1-3 and elafin were localized by immumohistochemistry in fetal membranes and placenta. Real-time quantitative PCR was used to examine mRNA expression in primary trophoblast cells treated with inflammatory molecules. HBD1-3 and elafin were immunolocalized to placenta] and chorion trophoblast layers of fetal membranes and placenta. Immunoreactivity was also observed in amnion epithelium and decidua. No differences were noted between samples from women who were not in tabour compared to those in active labour, In in vitro cultures of primary trophoblast cells, HBD2 and elafin mRNA expression was upregulated by the proinflammatory cytokine, IL-1 beta. These results suggest that the chorion and placental trophoblast layers may be key barriers to the progression of infection in the pregnant uterus. Natural antimicrobial expression may be altered in response to inflammatory mediator expression associated with the onset of labour and/or uterine infection, providing increased protection when the uterus may be particularly susceptible to infection. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:161 / 169
页数:9
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