Skip Navigation



Mol. Hum. Reprod. Advance Access published online on September 7, 2006

Molecular Human Reproduction, doi:10.1093/molehr/gal070
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
12/11/695    most recent
gal070v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Tyson-Capper, A. J.
Right arrow Articles by Loughney, A. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tyson-Capper, A. J.
Right arrow Articles by Loughney, A. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Received June 8, 2006
Accepted July 13, 2006

Article

Characterization of cellular retinoid-binding proteins in human myometrium during pregnancy

Alison J. Tyson-Capper 1 *, David M.W. Cork 1, Emily Wesley 1, Elizabeth A. Shiells 1, and Andrew D. Loughney 2

1 School of Surgical and Reproductive Sciences, The Medical School, University of Newcastle upon Tyne, UK
2 Women’s Services, Newcastle upon Tyne Hospitals NHS Trust, Royal Victoria Infirmary, Newcastle upon Tyne, UK

* To whom correspondence should be addressed.
Alison J. Tyson-Capper, E-mail: a.j.tyson-capper{at}ncl.ac.uk


   Abstract

Many complementary or competing signalling pathways bear an influence on the myometrium at any one time, and because the retinoic acid signalling pathway influences differentiation of a wide array of human tissues, this may be one of the determinants of myometrial differentiation during pregnancy. We have explored the novel hypothesis that the retinoids may act as important regulators in controlling the differentiated state of the human myometrium during pregnancy by characterizing the expression profiles for cellular retinoid-binding proteins CRBPI, CRABPI and CRABPII in non-pregnant, pregnant (non-labouring) and labouring human myometrium taken from the functionally distinct upper and lower uterine segments. In addition, we have investigated the effect of all-trans retinoic acid (ATRA) on the expression of several retinoic acid response genes including cyclooxygenase-2 (COX-2) and connexin-43 (Cx-43). Different spatial and temporal patterns of expression were observed for CRBPI, CRABPI and CRABPII within the upper and lower uterine segments through the three trimesters of pregnancy and in labour. Furthermore, the expression of COX-2, Cx-43, CRABPI, the transcription factor c-Jun and the retinoic acid receptor RAR{beta} altered in response to different concentrations of ATRA, suggesting that the differential expression of cellular retinoid-binding proteins may lead to different levels of retinoic acid being delivered to its nuclear targets, leading to the differential expression of specific target genes within the myometrium during pregnancy.

Keywords: all-trans retinoic acid/cellular retinoid-binding proteins/myometrium/parturition/pregnancy/retinoic acid.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Reproductive SciencesHome page
M. O'Brien, J. J. Morrison, and T. J. Smith
Upregulation of PSCDBP, TLR2, TWIST1, FLJ35382, EDNRB, and RGS12 Gene Expression in Human Myometrium at Labor
Reproductive Sciences, April 1, 2008; 15(4): 382 - 393.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.