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The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders

The aim of this study was to investigate the biological effects of sex hormones (17β-estradiol and testosterone) on rabbit articular chondrocytes from different genders. We cultured primary rabbit articular chondrocytes from both genders with varying concentration of sex hormones. We evaluate cell p...

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Detalles Bibliográficos
Autores principales: Chang, Shwu Jen, Kuo, Shyh Ming, Lin, Yen Ting, Yang, Shan-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065657/
https://www.ncbi.nlm.nih.gov/pubmed/24995337
http://dx.doi.org/10.1155/2014/932737
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author Chang, Shwu Jen
Kuo, Shyh Ming
Lin, Yen Ting
Yang, Shan-Wei
author_facet Chang, Shwu Jen
Kuo, Shyh Ming
Lin, Yen Ting
Yang, Shan-Wei
author_sort Chang, Shwu Jen
collection PubMed
description The aim of this study was to investigate the biological effects of sex hormones (17β-estradiol and testosterone) on rabbit articular chondrocytes from different genders. We cultured primary rabbit articular chondrocytes from both genders with varying concentration of sex hormones. We evaluate cell proliferation and biochemical functions by MTT and GAG assay. The chondrocyte function and phenotypes were analyzed by mRNA level using RT-PCR. Immunocytochemical staining was also used to evaluate the generation of collagen-II. This study demonstrated that 17β-estradiol had greater positive regulation on the biological function and gene expressions of articular chondrocytes than testosterone, with the optimal concentrations of 10(−6) and 10(−7) M, particularly for female chondrocytes.
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spelling pubmed-40656572014-07-03 The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders Chang, Shwu Jen Kuo, Shyh Ming Lin, Yen Ting Yang, Shan-Wei Biomed Res Int Research Article The aim of this study was to investigate the biological effects of sex hormones (17β-estradiol and testosterone) on rabbit articular chondrocytes from different genders. We cultured primary rabbit articular chondrocytes from both genders with varying concentration of sex hormones. We evaluate cell proliferation and biochemical functions by MTT and GAG assay. The chondrocyte function and phenotypes were analyzed by mRNA level using RT-PCR. Immunocytochemical staining was also used to evaluate the generation of collagen-II. This study demonstrated that 17β-estradiol had greater positive regulation on the biological function and gene expressions of articular chondrocytes than testosterone, with the optimal concentrations of 10(−6) and 10(−7) M, particularly for female chondrocytes. Hindawi Publishing Corporation 2014 2014-06-03 /pmc/articles/PMC4065657/ /pubmed/24995337 http://dx.doi.org/10.1155/2014/932737 Text en Copyright © 2014 Shwu Jen Chang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chang, Shwu Jen
Kuo, Shyh Ming
Lin, Yen Ting
Yang, Shan-Wei
The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders
title The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders
title_full The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders
title_fullStr The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders
title_full_unstemmed The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders
title_short The Biological Effects of Sex Hormones on Rabbit Articular Chondrocytes from Different Genders
title_sort biological effects of sex hormones on rabbit articular chondrocytes from different genders
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065657/
https://www.ncbi.nlm.nih.gov/pubmed/24995337
http://dx.doi.org/10.1155/2014/932737
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