학제간연구 | Interdisciplinary Studies in Gambling | 跨学科研究
- date : 2015-05-20 01:10|hit : 2083
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- Article] Comparative analysis of maternal-fetal interface in preeclampsia and preterm labor
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DocNo of ILP: 4140
Doc. Type: Article
Title: Comparative analysis of maternal-fetal interface in preeclampsia and preterm labor
Authors: Zhou, Y; Bianco, K; Huang, L; Nien, JK; McMaster, M; Romero, R; Fisher, SJ
Full Name of Authors: Zhou, Yan; Bianco, Katherine; Huang, Ling; Nien, Jyh K.; McMaster, Michael; Romero, Roberto; Fisher, Susan J.
Keywords by Author: pregnancy; preeclampsia; preterm birth; placenta; trophoblast; human
Keywords Plus: UTERINE ARTERY DOPPLER; PLACENTAL BED; G exPRESSION; CYTOTROPHOBLASTS; PATHOGENESIS; WOMEN; RISK; DIFFERENTIATION; HYPERTENSION; PREVENTION
Abstract: The maternal-fetal interface, a chimeric structure, is formed when fetal cytotrophoblasts (CTBs) from the placenta invade the uterine wall and its resident vasculature. In preeclampsia (PE), interstitial and endovascular invasion are often shallow, and fewer spiral arterioles are breached in toto. Our previous work has shown that faulty CTB differentiation to an invasive phenotype is a contributing factor. Here, we have tested the hypothesis that the constellation of morphological and molecular defects that are associated with PE are unique to this condition. Specifically, we have compared the histology of the maternal-fetal interface and CTB expression of stage-specific antigens in PE and in preterm labor (PTL) with or without inflammation. In the absence of inflammation, biopsies obtained after PTL were near normal at histological and molecular levels. In accord with previously published data, PE had severe negative effects on the endpoints analyzed. Biopsies obtained after PTL with inflammation had an intermediate phenotype. Our results suggest that the maternal-fetal interface from cases of PTL without inflammation can be used for comparative purposes, e.g., as age-matched controls, in studies of the effects of PE on cells in this region.
Cate of OECD: Biological sciences
Year of Publication: 2007
Business Area: other
Detail Business: medicine & science
Country: USA
Study Area:
Name of Journal: CELL AND TISSUE RESEARCH
Language: English
Country of Authors: Univ Calif San Francisco, San Francisco, CA 94143 USA; Univ Calif San Francisco, Dept Cell & Tissue Biol, San Francisco, CA 94143 USA; Univ Calif San Francisco, Dept Obstet Gynecol & Reprod Sci, San Francisco, CA 94143 USA; NICHHD, NIH, Perinatol Res Branch, Dept Hlth & Human Serv, Detroit, MI USA; Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA; Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Press Adress: Fisher, SJ (reprint author), Univ Calif San Francisco, 513 Parnassus Ave,HSE 1619, San Francisco, CA 94143 USA.
Email Address: sfisher@cgl.ucsf.edu
Citaion:
Funding:
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Number of Citaion: 40
Publication: SPRINGER
City of Publication: NEW YORK
Address of Publication: 233 SPRING STREET, NEW YORK, NY 10013 USA
ISSN: 0302-766X
29-Character Source Abbreviation: CELL TISSUE RES
ISO Source Abbreviation: Cell Tissue Res.
Volume: 329
Version: 3
Start of File: 559
End of File: 569
DOI: 10.1007/s00441-007-0428-0
Number of Pages: 11
Web of Science Category: Cell Biology
Subject Category: Cell Biology
Document Delivery Number: 205PZ
Unique Article Identifier: WOS:000249128400013
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