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Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue

BACKGROUND: Inhibins are important regulators of the female reproductive system. Recently, two new inhibin subunits betaC and betaE have been described, although it is unclear if they are synthesized in normal human endometrium. METHODS: Samples of human endometrium were obtained from 82 premenopaus...

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Autores principales: Mylonas, Ioannis, Brüning, Ansgar, Shabani, Naim, Kunze, Susanne, Kupka, Markus S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002354/
https://www.ncbi.nlm.nih.gov/pubmed/21092084
http://dx.doi.org/10.1186/1477-7827-8-143
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author Mylonas, Ioannis
Brüning, Ansgar
Shabani, Naim
Kunze, Susanne
Kupka, Markus S
author_facet Mylonas, Ioannis
Brüning, Ansgar
Shabani, Naim
Kunze, Susanne
Kupka, Markus S
author_sort Mylonas, Ioannis
collection PubMed
description BACKGROUND: Inhibins are important regulators of the female reproductive system. Recently, two new inhibin subunits betaC and betaE have been described, although it is unclear if they are synthesized in normal human endometrium. METHODS: Samples of human endometrium were obtained from 82 premenopausal, non-pregnant patients undergoing gynecological surgery for benign diseases. Endometrium samples were classified according to anamnestic and histological dating into proliferative (day 1-14, n = 46), early secretory (day 15-22, n = 18) and late secretory phase (day 23-28, n = 18). Immunohistochemical analyses were performed with specific antibodies against inhibin alpha (n = 81) as well as inhibin betaA (n = 82), betaB (n = 82), betaC (n = 74) and betaE (n = 76) subunits. RT-PCR was performed for all inhibin subunits. Correlation was assessed with the Spearman factor to assess the relationship of inhibin-subunits expression within the different endometrial samples. RESULTS: The novel inhibin betaC and betaE subunits were found in normal human endometrium by immunohistochemical and molecular techniques. Inhibin alpha, betaA, betaB and betaE subunits showed a circadian expression pattern, being more abundant during the late secretory phase than during the proliferative phase. Additionally, a significant correlation between inhibin alpha and all inhibin beta subunits was observed. CONCLUSIONS: The differential expression pattern of the betaC- and betaE-subunits in normal human endometrial tissue suggests that they function in endometrial maturation and blastocyst implantation. However, the precise role of these novel inhibin/activin subunits in human endometrium is unclear and warrants further investigation.
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spelling pubmed-30023542010-12-16 Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue Mylonas, Ioannis Brüning, Ansgar Shabani, Naim Kunze, Susanne Kupka, Markus S Reprod Biol Endocrinol Research BACKGROUND: Inhibins are important regulators of the female reproductive system. Recently, two new inhibin subunits betaC and betaE have been described, although it is unclear if they are synthesized in normal human endometrium. METHODS: Samples of human endometrium were obtained from 82 premenopausal, non-pregnant patients undergoing gynecological surgery for benign diseases. Endometrium samples were classified according to anamnestic and histological dating into proliferative (day 1-14, n = 46), early secretory (day 15-22, n = 18) and late secretory phase (day 23-28, n = 18). Immunohistochemical analyses were performed with specific antibodies against inhibin alpha (n = 81) as well as inhibin betaA (n = 82), betaB (n = 82), betaC (n = 74) and betaE (n = 76) subunits. RT-PCR was performed for all inhibin subunits. Correlation was assessed with the Spearman factor to assess the relationship of inhibin-subunits expression within the different endometrial samples. RESULTS: The novel inhibin betaC and betaE subunits were found in normal human endometrium by immunohistochemical and molecular techniques. Inhibin alpha, betaA, betaB and betaE subunits showed a circadian expression pattern, being more abundant during the late secretory phase than during the proliferative phase. Additionally, a significant correlation between inhibin alpha and all inhibin beta subunits was observed. CONCLUSIONS: The differential expression pattern of the betaC- and betaE-subunits in normal human endometrial tissue suggests that they function in endometrial maturation and blastocyst implantation. However, the precise role of these novel inhibin/activin subunits in human endometrium is unclear and warrants further investigation. BioMed Central 2010-11-19 /pmc/articles/PMC3002354/ /pubmed/21092084 http://dx.doi.org/10.1186/1477-7827-8-143 Text en Copyright ©2010 Mylonas et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Mylonas, Ioannis
Brüning, Ansgar
Shabani, Naim
Kunze, Susanne
Kupka, Markus S
Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue
title Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue
title_full Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue
title_fullStr Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue
title_full_unstemmed Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue
title_short Evidence of inhibin/activin subunit betaC and betaE synthesis in normal human endometrial tissue
title_sort evidence of inhibin/activin subunit betac and betae synthesis in normal human endometrial tissue
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002354/
https://www.ncbi.nlm.nih.gov/pubmed/21092084
http://dx.doi.org/10.1186/1477-7827-8-143
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