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Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome

The failure of reproductive success in polycystic ovary syndrome (PCOS) patients could be in part due to endometrial dysfunction. However, no studies have investigated any causality between androgen, androgen receptor (AR) expression, and adenosine monophosphate activated protein kinase (AMPK) activ...

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Autores principales: Li, Xin, Pishdari, Bano, Cui, Peng, Hu, Min, Yang, Hong-Ping, Guo, Yan-Rong, Jiang, Hong-Yuan, Feng, Yi, Billig, Håkan, Shao, Ruijin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671995/
https://www.ncbi.nlm.nih.gov/pubmed/26681917
http://dx.doi.org/10.7150/ijbs.13109
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author Li, Xin
Pishdari, Bano
Cui, Peng
Hu, Min
Yang, Hong-Ping
Guo, Yan-Rong
Jiang, Hong-Yuan
Feng, Yi
Billig, Håkan
Shao, Ruijin
author_facet Li, Xin
Pishdari, Bano
Cui, Peng
Hu, Min
Yang, Hong-Ping
Guo, Yan-Rong
Jiang, Hong-Yuan
Feng, Yi
Billig, Håkan
Shao, Ruijin
author_sort Li, Xin
collection PubMed
description The failure of reproductive success in polycystic ovary syndrome (PCOS) patients could be in part due to endometrial dysfunction. However, no studies have investigated any causality between androgen, androgen receptor (AR) expression, and adenosine monophosphate activated protein kinase (AMPK) activation in the endometrium under physiological and pathological conditions. In the present study, we show that 1) endometrial AR expression levels fluctuate in non-PCOS and PCOS patients during the menstrual cycle; 2) the menstrual phase-dependent alteration of p-AMPKα expression occurs in non-PCOS patients but not in PCOS patients; 3) AR expression is higher in PCOS patients than non-PCOS patients during hyperplasia while AMPKα activation (indicated by the ratio of p-AMPKα to AMPKα); and 4) co-localization of AR and Ki-67 in epithelial cell nuclei is observed in endometrial hyperplasia. Importantly, using in vitro human tissue culture and an in vivo 5α-dihydrotestosterone-treated rat model, we show that the action of androgen on AMPKα activation is likely mediated through nuclear AR, especially in epithelial cells. Collectively, we present evidence that AR expression and AMPKα activation depend on menstrual cycle phase and the presence of PCOS, and the data suggest that AR-mediated regulation of AMPKα activation might play a role in the development of endometrial hyperplasia.
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spelling pubmed-46719952015-12-17 Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome Li, Xin Pishdari, Bano Cui, Peng Hu, Min Yang, Hong-Ping Guo, Yan-Rong Jiang, Hong-Yuan Feng, Yi Billig, Håkan Shao, Ruijin Int J Biol Sci Research Paper The failure of reproductive success in polycystic ovary syndrome (PCOS) patients could be in part due to endometrial dysfunction. However, no studies have investigated any causality between androgen, androgen receptor (AR) expression, and adenosine monophosphate activated protein kinase (AMPK) activation in the endometrium under physiological and pathological conditions. In the present study, we show that 1) endometrial AR expression levels fluctuate in non-PCOS and PCOS patients during the menstrual cycle; 2) the menstrual phase-dependent alteration of p-AMPKα expression occurs in non-PCOS patients but not in PCOS patients; 3) AR expression is higher in PCOS patients than non-PCOS patients during hyperplasia while AMPKα activation (indicated by the ratio of p-AMPKα to AMPKα); and 4) co-localization of AR and Ki-67 in epithelial cell nuclei is observed in endometrial hyperplasia. Importantly, using in vitro human tissue culture and an in vivo 5α-dihydrotestosterone-treated rat model, we show that the action of androgen on AMPKα activation is likely mediated through nuclear AR, especially in epithelial cells. Collectively, we present evidence that AR expression and AMPKα activation depend on menstrual cycle phase and the presence of PCOS, and the data suggest that AR-mediated regulation of AMPKα activation might play a role in the development of endometrial hyperplasia. Ivyspring International Publisher 2015-11-01 /pmc/articles/PMC4671995/ /pubmed/26681917 http://dx.doi.org/10.7150/ijbs.13109 Text en © 2015 Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions.
spellingShingle Research Paper
Li, Xin
Pishdari, Bano
Cui, Peng
Hu, Min
Yang, Hong-Ping
Guo, Yan-Rong
Jiang, Hong-Yuan
Feng, Yi
Billig, Håkan
Shao, Ruijin
Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome
title Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome
title_full Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome
title_fullStr Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome
title_full_unstemmed Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome
title_short Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome
title_sort regulation of androgen receptor expression alters ampk phosphorylation in the endometrium: in vivo and in vitro studies in women with polycystic ovary syndrome
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671995/
https://www.ncbi.nlm.nih.gov/pubmed/26681917
http://dx.doi.org/10.7150/ijbs.13109
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