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Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum
BACKGROUND: Estradiol plays an important role in the regulation of collagen metabolism. Deficiency of estradiol has been reported to be associated with the degeneration of many connective tissues. However, the association of estradiol and hypertrophy of the ligamentum flavum was seldom explored. The...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108226/ https://www.ncbi.nlm.nih.gov/pubmed/25022571 http://dx.doi.org/10.1186/1471-2474-15-238 |
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author | Chen, Mei-Hsiu Hu, Chao-Kai Chen, Pei-Ru Chen, Yu-Shan Sun, Jui-Sheng Chen, Ming-Hong |
author_facet | Chen, Mei-Hsiu Hu, Chao-Kai Chen, Pei-Ru Chen, Yu-Shan Sun, Jui-Sheng Chen, Ming-Hong |
author_sort | Chen, Mei-Hsiu |
collection | PubMed |
description | BACKGROUND: Estradiol plays an important role in the regulation of collagen metabolism. Deficiency of estradiol has been reported to be associated with the degeneration of many connective tissues. However, the association of estradiol and hypertrophy of the ligamentum flavum was seldom explored. Therefore, we studied the effects of estradiol on cultured cells from the ligamentum flavum. METHODS: Primary cultures of human ligamentum flavum cells obtained from surgical specimens of 14 patients undergoing spinal surgery were used to investigate the effect of estradiol on cell proliferation and the expression of collagen, elastin, and matrix metalloproteinases. Downstream pathways of estrogen receptor underlying the regulation of metalloproteinases were also investigated. RESULTS: In our study, we revealed the existence of estrogen receptors on both female and male ligamentum flavum cells with a gender difference. 17β-estradiol increased early (24 hours) proliferation of ligamentum flavum cells in a dose dependent manner and the effect could not be seen when the cell density increased. Estradiol with a concentration of 10(-9) M decreased collagen levels and increased the expression of MMP-13. Adding an antagonist of PI3K downstream pathway could reverse the expression of MMP-13 caused by estradiol. CONCLUSIONS: The results implied estradiol regulated the expression of MMP-13 via PI3K pathway and contributed to the homeostasis of extracellular matrix in the ligamentum flavum. |
format | Online Article Text |
id | pubmed-4108226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41082262014-07-24 Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum Chen, Mei-Hsiu Hu, Chao-Kai Chen, Pei-Ru Chen, Yu-Shan Sun, Jui-Sheng Chen, Ming-Hong BMC Musculoskelet Disord Research Article BACKGROUND: Estradiol plays an important role in the regulation of collagen metabolism. Deficiency of estradiol has been reported to be associated with the degeneration of many connective tissues. However, the association of estradiol and hypertrophy of the ligamentum flavum was seldom explored. Therefore, we studied the effects of estradiol on cultured cells from the ligamentum flavum. METHODS: Primary cultures of human ligamentum flavum cells obtained from surgical specimens of 14 patients undergoing spinal surgery were used to investigate the effect of estradiol on cell proliferation and the expression of collagen, elastin, and matrix metalloproteinases. Downstream pathways of estrogen receptor underlying the regulation of metalloproteinases were also investigated. RESULTS: In our study, we revealed the existence of estrogen receptors on both female and male ligamentum flavum cells with a gender difference. 17β-estradiol increased early (24 hours) proliferation of ligamentum flavum cells in a dose dependent manner and the effect could not be seen when the cell density increased. Estradiol with a concentration of 10(-9) M decreased collagen levels and increased the expression of MMP-13. Adding an antagonist of PI3K downstream pathway could reverse the expression of MMP-13 caused by estradiol. CONCLUSIONS: The results implied estradiol regulated the expression of MMP-13 via PI3K pathway and contributed to the homeostasis of extracellular matrix in the ligamentum flavum. BioMed Central 2014-07-15 /pmc/articles/PMC4108226/ /pubmed/25022571 http://dx.doi.org/10.1186/1471-2474-15-238 Text en Copyright © 2014 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Chen, Mei-Hsiu Hu, Chao-Kai Chen, Pei-Ru Chen, Yu-Shan Sun, Jui-Sheng Chen, Ming-Hong Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum |
title | Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum |
title_full | Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum |
title_fullStr | Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum |
title_full_unstemmed | Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum |
title_short | Dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum |
title_sort | dose-dependent regulation of cell proliferation and collagen degradation by estradiol on ligamentum flavum |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108226/ https://www.ncbi.nlm.nih.gov/pubmed/25022571 http://dx.doi.org/10.1186/1471-2474-15-238 |
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