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Sex differences influence intestinal epithelial stem cell proliferation independent of obesity
The intestinal epithelium is continuously regenerated by cell renewal of intestinal epithelial stem cells (IESCs) located in the intestinal crypts. Obesity affects this process and results in changes in the size and cellular make‐up of the tissue, but it remains unknown if there are sex differences...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021372/ https://www.ncbi.nlm.nih.gov/pubmed/29952094 http://dx.doi.org/10.14814/phy2.13746 |
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author | Zhou, Weinan Davis, Elizabeth A. Li, Kailiang Nowak, Romana A. Dailey, Megan J. |
author_facet | Zhou, Weinan Davis, Elizabeth A. Li, Kailiang Nowak, Romana A. Dailey, Megan J. |
author_sort | Zhou, Weinan |
collection | PubMed |
description | The intestinal epithelium is continuously regenerated by cell renewal of intestinal epithelial stem cells (IESCs) located in the intestinal crypts. Obesity affects this process and results in changes in the size and cellular make‐up of the tissue, but it remains unknown if there are sex differences in obesity‐induced alterations in IESC proliferation and differentiation. We fed male and female mice a 60% high‐fat diet (HFD) or a 10% low‐fat diet (LFD) for 3 months and investigated the differences in (1) the expression of markers of different intestinal epithelial cell types in vivo, and (2) lasting effects on IESC growth in vitro. We found that the growth of IESCs in vitro were enhanced in females compared with males. HFD induced similar in vivo changes and in vitro early growth of IESCs in males and females. The IESCs isolated and grown in vitro from females, though, showed an enhanced growth that was independent of obesity. To determine whether this effect was driven by sex steroid hormones, we used primary intestinal crypts isolated from male and female mice and investigated the differences in (1) the expression of steroid hormone receptors, and (2) cell proliferation in response to steroid hormones. We found that estrogen receptor α was expressed in crypts from both sexes, but estrogen had no effect on proliferation in either sex. These results suggest that obesity similarly effects IESCs in males and females, but IESCs in females have greater proliferation ability than males, but this is not driven by a direct effect of sex steroid hormones on IESCs or other crypt cells that provide essential niche support for IESCs. |
format | Online Article Text |
id | pubmed-6021372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60213722018-07-06 Sex differences influence intestinal epithelial stem cell proliferation independent of obesity Zhou, Weinan Davis, Elizabeth A. Li, Kailiang Nowak, Romana A. Dailey, Megan J. Physiol Rep Original Research The intestinal epithelium is continuously regenerated by cell renewal of intestinal epithelial stem cells (IESCs) located in the intestinal crypts. Obesity affects this process and results in changes in the size and cellular make‐up of the tissue, but it remains unknown if there are sex differences in obesity‐induced alterations in IESC proliferation and differentiation. We fed male and female mice a 60% high‐fat diet (HFD) or a 10% low‐fat diet (LFD) for 3 months and investigated the differences in (1) the expression of markers of different intestinal epithelial cell types in vivo, and (2) lasting effects on IESC growth in vitro. We found that the growth of IESCs in vitro were enhanced in females compared with males. HFD induced similar in vivo changes and in vitro early growth of IESCs in males and females. The IESCs isolated and grown in vitro from females, though, showed an enhanced growth that was independent of obesity. To determine whether this effect was driven by sex steroid hormones, we used primary intestinal crypts isolated from male and female mice and investigated the differences in (1) the expression of steroid hormone receptors, and (2) cell proliferation in response to steroid hormones. We found that estrogen receptor α was expressed in crypts from both sexes, but estrogen had no effect on proliferation in either sex. These results suggest that obesity similarly effects IESCs in males and females, but IESCs in females have greater proliferation ability than males, but this is not driven by a direct effect of sex steroid hormones on IESCs or other crypt cells that provide essential niche support for IESCs. John Wiley and Sons Inc. 2018-06-27 /pmc/articles/PMC6021372/ /pubmed/29952094 http://dx.doi.org/10.14814/phy2.13746 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Zhou, Weinan Davis, Elizabeth A. Li, Kailiang Nowak, Romana A. Dailey, Megan J. Sex differences influence intestinal epithelial stem cell proliferation independent of obesity |
title | Sex differences influence intestinal epithelial stem cell proliferation independent of obesity |
title_full | Sex differences influence intestinal epithelial stem cell proliferation independent of obesity |
title_fullStr | Sex differences influence intestinal epithelial stem cell proliferation independent of obesity |
title_full_unstemmed | Sex differences influence intestinal epithelial stem cell proliferation independent of obesity |
title_short | Sex differences influence intestinal epithelial stem cell proliferation independent of obesity |
title_sort | sex differences influence intestinal epithelial stem cell proliferation independent of obesity |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021372/ https://www.ncbi.nlm.nih.gov/pubmed/29952094 http://dx.doi.org/10.14814/phy2.13746 |
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