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Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) levels: A cross-sectional study
Women have higher adiposity but maintain insulin sensitivity when compared to men. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) inhibits insulin signaling, but it is not known if PTEN regulate insulin resistance in a sex-specific manner. In this cross-sectional study, muscle biopsi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366049/ https://www.ncbi.nlm.nih.gov/pubmed/25777795 http://dx.doi.org/10.1038/srep09154 |
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author | Samaan, M. Constantine Anand, Sonia S. Sharma, Arya M. Samjoo, Imtiaz A. Tarnopolsky, Mark A. |
author_facet | Samaan, M. Constantine Anand, Sonia S. Sharma, Arya M. Samjoo, Imtiaz A. Tarnopolsky, Mark A. |
author_sort | Samaan, M. Constantine |
collection | PubMed |
description | Women have higher adiposity but maintain insulin sensitivity when compared to men. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) inhibits insulin signaling, but it is not known if PTEN regulate insulin resistance in a sex-specific manner. In this cross-sectional study, muscle biopsies from participants in the Molecular Study of Health and Risk in Ethnic Groups (Mol-SHARE) were used to test for sex differences in PTEN expression. Quantitative real-time PCR was performed to determine PTEN gene expression (n = 53), and western blotting detected total and phosphorylated PTEN protein (n = 36). Study participants were comparable in age and body mass index. Women had higher fat mass percentage compared to men (40.25 ± 9.9% in women versus 27.6 ± 8.8% in men; mean difference −0.18, 95%CI (−0.24, −0.11), p-value <0.0001), with similar HOMA-IR (2.46 ± 2.05 in men versus 2.34 ± 3.06 in women; mean difference 0.04; 95% CI (−0.12, 0.21), p-value 0.59). Women had significant downregulation of PTEN gene expression (p-value 0.01) and upregulation of PTEN protein phosphorylation (inactivation) (p-value 0.001) when compared to men after correction for age, ethnicity, HOMA-IR, fat mass and sex. We conclude that the downregulation of muscle PTEN may explain the retention of insulin sensitivity with higher adiposity in women compared to men. |
format | Online Article Text |
id | pubmed-4366049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43660492015-03-31 Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) levels: A cross-sectional study Samaan, M. Constantine Anand, Sonia S. Sharma, Arya M. Samjoo, Imtiaz A. Tarnopolsky, Mark A. Sci Rep Article Women have higher adiposity but maintain insulin sensitivity when compared to men. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) inhibits insulin signaling, but it is not known if PTEN regulate insulin resistance in a sex-specific manner. In this cross-sectional study, muscle biopsies from participants in the Molecular Study of Health and Risk in Ethnic Groups (Mol-SHARE) were used to test for sex differences in PTEN expression. Quantitative real-time PCR was performed to determine PTEN gene expression (n = 53), and western blotting detected total and phosphorylated PTEN protein (n = 36). Study participants were comparable in age and body mass index. Women had higher fat mass percentage compared to men (40.25 ± 9.9% in women versus 27.6 ± 8.8% in men; mean difference −0.18, 95%CI (−0.24, −0.11), p-value <0.0001), with similar HOMA-IR (2.46 ± 2.05 in men versus 2.34 ± 3.06 in women; mean difference 0.04; 95% CI (−0.12, 0.21), p-value 0.59). Women had significant downregulation of PTEN gene expression (p-value 0.01) and upregulation of PTEN protein phosphorylation (inactivation) (p-value 0.001) when compared to men after correction for age, ethnicity, HOMA-IR, fat mass and sex. We conclude that the downregulation of muscle PTEN may explain the retention of insulin sensitivity with higher adiposity in women compared to men. Nature Publishing Group 2015-03-17 /pmc/articles/PMC4366049/ /pubmed/25777795 http://dx.doi.org/10.1038/srep09154 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Samaan, M. Constantine Anand, Sonia S. Sharma, Arya M. Samjoo, Imtiaz A. Tarnopolsky, Mark A. Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) levels: A cross-sectional study |
title | Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome
10 (PTEN) levels: A cross-sectional study |
title_full | Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome
10 (PTEN) levels: A cross-sectional study |
title_fullStr | Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome
10 (PTEN) levels: A cross-sectional study |
title_full_unstemmed | Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome
10 (PTEN) levels: A cross-sectional study |
title_short | Sex differences in skeletal muscle Phosphatase and tensin homolog deleted on chromosome
10 (PTEN) levels: A cross-sectional study |
title_sort | sex differences in skeletal muscle phosphatase and tensin homolog deleted on chromosome
10 (pten) levels: a cross-sectional study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366049/ https://www.ncbi.nlm.nih.gov/pubmed/25777795 http://dx.doi.org/10.1038/srep09154 |
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