Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (13)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Nasu, K.
Right arrow Articles by Miyakawa, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nasu, K.
Right arrow Articles by Miyakawa, I.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Human Reproduction, Vol. 7, No. 8, 741-746, August 2001
© 2001 European Society of Human Reproduction and Embryology


Uterine physiology

Expression and regulation of growth-regulated oncogene {alpha} in human endometrial stromal cells

Kaei Nasu,1, Kayo Fujisawa, Kazuyo Arima, Kengo Kai, Terumasa Sugano and Isao Miyakawa

Department of Obstetrics and Gynecology, Oita Medical University, Hasama-machi, Oita 879-5593, Japan

Abstract

Growth-regulated oncogene {alpha} (GRO{alpha}), a potent chemoattractant for neutrophils, has previously been detected in the endometrial stromal cells (ESC) of human endometrium. In this study, the mRNA expression of GRO{alpha} in the endometrium was evaluated by reverse transcription–polymerase chain reaction analysis, while the localization of GRO{alpha} protein was studied by immunohistochemistry and the concentrations of GRO{alpha} were measured using an enzyme-linked immunosorbent assay (ELISA). The effects of known modulators of endometrial function on the production of GRO{alpha} by ESC were also examined by ELISA and Northern blot analysis. The expression of both GRO{alpha} mRNA and GRO{alpha} protein was detected in the cycling endometrium. GRO{alpha} protein was localized mainly in the stroma, and endometrial tissues in the secretory phase contained higher amounts of GRO{alpha} protein than did those in the proliferative phase. The production of GRO{alpha} by ESC was enhanced by in-vitro decidualization. Lipopolysaccharide, tumour necrosis factor-{alpha} and interleukin-1ß also stimulated the expression of GRO{alpha} mRNA and protein by ESC. These results suggest that the production of GRO{alpha} by ESC is regulated by ovarian steroid hormones as well as by inflammatory mediators. The modulation of GRO{alpha} concentrations in the local environment may contribute to normal and pathological processes in the uterus by regulating leukocyte trafficking in the endometrium.

cytokine network/endometrial stromal cell/growth-regulated oncogene {alpha}/menstrual cycle

Notes

1 To whom correspondence should be addressed. E-mail: nasu{at}oita-med.ac.jp


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
Biol. Reprod.Home page
C.-w. Cheng, H. Bielby, D. Licence, S. K. Smith, C. G. Print, and D. S. Charnock-Jones
Quantitative Cellular and Molecular Analysis of the Effect of Progesterone Withdrawal in a Murine Model of Decidualization
Biol Reprod, May 1, 2007; 76(5): 871 - 883.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
A.P. Hess, A.E. Hamilton, S. Talbi, C. Dosiou, M. Nyegaard, N. Nayak, O. Genbecev-Krtolica, P. Mavrogianis, K. Ferrer, J. Kruessel, et al.
Decidual Stromal Cell Response to Paracrine Signals from the Trophoblast: Amplification of Immune and Angiogenic Modulators
Biol Reprod, January 1, 2007; 76(1): 102 - 117.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
M. Rossi, A. M Sharkey, P. Vigano, G. Fiore, R. Furlong, P. Florio, G. Ambrosini, S. K Smith, and F. Petraglia
Identification of genes regulated by interleukin-1{beta} in human endometrial stromal cells
Reproduction, November 1, 2005; 130(5): 721 - 729.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
M. Nishida, K. Nasu, J. Fukuda, Y. Kawano, H. Narahara, and I. Miyakawa
Down-Regulation of Interleukin-1 Receptor Type 1 Expression Causes the Dysregulated Expression of CXC Chemokines in Endometriotic Stromal Cells: A Possible Mechanism for the Altered Immunological Functions in Endometriosis
J. Clin. Endocrinol. Metab., October 1, 2004; 89(10): 5094 - 5100.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
K. Kitaya, T. Nakayama, N. Daikoku, S. Fushiki, and H. Honjo
Spatial and Temporal Expression of Ligands for CXCR3 and CXCR4 in Human Endometrium
J. Clin. Endocrinol. Metab., May 1, 2004; 89(5): 2470 - 2476.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
K. Kitaya, T. Nakayama, T. Okubo, H. Kuroboshi, S. Fushiki, and H. Honjo
Expression of Macrophage Inflammatory Protein-1{beta} in Human Endometrium: Its Role in Endometrial Recruitment of Natural Killer Cells
J. Clin. Endocrinol. Metab., April 1, 2003; 88(4): 1809 - 1814.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
B. Sun, K. Nasu, J. Fukuda, S. Mine, M. Nishida, and I. Miyakawa
Expression of macrophage inflammatory protein-3{alpha} in an endometrial epithelial cell line, HHUA, and cultured human endometrial stromal cells
Mol. Hum. Reprod., October 1, 2002; 8(10): 930 - 933.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
K. Kai, K. Nasu, S. Nakamura, J. Fukuda, M. Nishida, and I. Miyakawa
Expression of interferon-{gamma}-inducible protein-10 in human endometrial stromal cells
Mol. Hum. Reprod., February 1, 2002; 8(2): 176 - 180.
[Abstract] [Full Text] [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.