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Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/1669

Title: The progesterone receptor in human term amniochorion and placenta is isoform C.
Authors: Taylor, Anthony H.
McParland, Penny C.
Taylor, David J.
Bell, Stephen C.
Issue Date: 27-Oct-2005
Publisher: The Endocrine Society
Citation: Endocrinology, 2006, 147 (2), pp.687-693
Abstract: The mechanism that initiates human parturition has been proposed to be functional progesterone withdrawal whereby the 116-kDa B-isoform of the progesterone receptor (PR-B) switches in favor of the 94-kDa A-isoform (PR-A) in reproductive tissues. Recently other PR isoforms, PR-S, PR-C, and PR-M generated from the same gene have been identified and partially characterized. Using immunohistochemical, Western blotting, and RT-PCR techniques, evidence is provided that the major PR isoform present in human term fetal membranes (amnion and chorion) and syncytiotrophoblast of the placenta is neither of the classical nuclear PR-B or PR-A isoforms but is the N terminally truncated 60-kDa PR-C isoform. Evidence is also provided that the PR-C isoform resides in the cytoplasm of the expressing cell types. Data are also presented to show that PR-B, PR-A, and PR-S isoforms are essentially absent from the amnion and chorion, whereas PR isoforms A, B, C, and S are all present in the decidua, with PR-A being the major isoform. The syncytiotrophoblast of the placenta contains the cytoplasmic PR-C isoform but not PR-A, PR-B, or PR-S. The major PR isoform in the amnion, chorion, and placenta is PR-C, suggesting that the cytoplasmic PR-C isoform has a specific role in extraembryonic tissues and may be involved in the regulation of human parturition.
DOI Link: 10.1210/en.2005-0510
ISSN: 0013-7227
eISSN: 1945-7170
Links: http://hdl.handle.net/2381/1669
http://endo.endojournals.org/content/147/(...)
Version: Publisher Version
Status: Peer-reviewed
Type: Article
Rights: Copyright © 2005, The Endocrine Society. Deposited with reference to the publisher’s archiving policy available on the SHERPA/RoMEO website.
Appears in Collections:Published Articles, Dept. of Cancer Studies and Molecular Medicine

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