Reproduction  
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  

Reproduction (2007) 133 1213-1221
DOI: 10.1530/REP-07-0085
Copyright © 2007 Society for Reproduction and Fertility
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Herington, J. L
Right arrow Articles by Bany, B. M
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Herington, J. L
Right arrow Articles by Bany, B. M

RESEARCH

The conceptus increases secreted phosphoprotein 1 gene expression in the mouse uterus during the progression of decidualization mainly due to its effects on uterine natural killer cells

Jennifer L Herington and Brent M Bany

Department of Physiology, Southern Illinois University School of Medicine, Carbondale, Illinois 62901, USA

Correspondence should be addressed to B M Bany; Email: bbany{at}siumed.edu

Within the mouse endometrium, secreted phosphoprotein 1 (SPP1) gene expression is mainly expressed in the luminal epithelium and some macrophages around the onset of implantation. However, during the progression of decidualization, it is expressed mainly in the mesometrial decidua. To date, the precise cell types responsible for the expression in the mesometrial decidua has not been absolutely identified. The goal of the present study was to assess the expression of SPP1 in uteri of pregnant mice (decidua) during the progression of decidualization and compared it with those undergoing artificially induced decidualization (deciduoma). Significantly (P<0.05) greater steady-state levels of SPP1 mRNA were seen in the decidua when compared with deciduoma. Further, in the decidua, the majority of the SPP1 protein was localized within a subpopulation of granulated uterine natural killer (uNK) cells but not co-localized to their granules. However, in addition to being localized to uNK cells, SPP1 protein was also detected in another cell type(s) that were not epidermal growth factor-like containing mucin-like hormone receptor-like sequence 1 protein-positive immune cells that are known to be present in the uterus at this time. Finally, decidual SPP1 expression dramatically decreased in uteri of interleukin-15-deficient mice that lack uNK cells. In conclusion, SPP1 expression is greater in the mouse decidua when compared with the deciduoma after the onset of implantation during the progression of decidualization. Finally, uNK cells were found to be the major source of SPP1 in the pregnant uterus during decidualization. SPP1 might play a key role in uNK killer cell functions in the uterus during decidualization.




This article has been cited by other articles:


Home page
EndocrinologyHome page
J. L. Herington, T. Underwood, M. McConaha, and B. M. Bany
Paracrine Signals from the Mouse Conceptus Are Not Required for the Normal Progression of Decidualization
Endocrinology, September 1, 2009; 150(9): 4404 - 4413.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
A. Franchi, J. Zaret, X. Zhang, S. Bocca, and S. Oehninger
Expression of immunomodulatory genes, their protein products and specific ligands/receptors during the window of implantation in the human endometrium
Mol. Hum. Reprod., July 1, 2008; 14(7): 413 - 421.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  
Copyright © 2007 by the Society for Reproduction and Fertility.