Back to Search Start Over

Inhibin/activin subunits alpha, beta-A and beta-B are differentially expressed in normal human endometrium throughout the menstrual cycle.

Authors :
Mylonas, Ioannis
Jeschke, Udo
Wiest, Irmgard
Hoeing, Anna
Vogl, Julia
Shabani, Naim
Kuhn, Christina
Schulze, Sandra
Kupka, Markus S.
Friese, Klaus
Source :
Histochemistry & Cell Biology; Nov2004, Vol. 122 Issue 5, p461-471, 11p
Publication Year :
2004

Abstract

Inhibins are dimeric glycoproteins composed of an alpha (α) subunit and one of two possible beta (β) subunits (βA or βB). The aims of this study were to assess the frequency and tissue distribution patterns of the inhibin subunits in normal human endometrium. Samples from human endometrium from proliferative phase (PP; n=32), early secretory phase (ES; n=1O) and late secretory phase (LS; n=1 2) were obtained. Immunohistochemistry, immunofluorescence and a statistical analysis were performed. All three inhibin subunits were expressed by normal endometrium by immunohistochemistry and immunofluorescence. Inhibin-a was primarily detected in glandular epithelial cells, while inhibin-β subunits were additionally localised in stromal tissue. Inhibin-a staining reaction increased significantly between PP and ES (P<0.05), PP and LS (P<0.01), and ES and LS (P<0.02). Inhibin-βA and -βB were significant higher in LS than PP (P<0.05) and LS than ES (P<0.05). All three inhibin subunits were expressed by human endometrium varying across the menstrual cycle. This suggests substantial functions in human implantation of inhibin-α subunit, while stromal expression of the β subunits could be important in the paracrine signalling for adequate endometrial maturation. The distinct expression in human endometrial tissue suggests a synthesis of inhibins into the lumen and a predominant secretion of activins into the stroma. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09486143
Volume :
122
Issue :
5
Database :
Complementary Index
Journal :
Histochemistry & Cell Biology
Publication Type :
Academic Journal
Accession number :
15108283
Full Text :
https://doi.org/10.1007/s00418-004-0709-6