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Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro
To investigate the effects of silica on circulating fibrocytes (cFbs), the present study established a primary culture model of rat alveolar macrophages and cFbs in vitro. Macrophages were treated with free silica, and their supernatant was used to stimulate cFbs. The mRNA expression levels of colla...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581811/ https://www.ncbi.nlm.nih.gov/pubmed/26299717 http://dx.doi.org/10.3892/mmr.2015.4212 |
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author | YAO, WU LIU, SUNA LI, JU HAO, CHANGFU |
author_facet | YAO, WU LIU, SUNA LI, JU HAO, CHANGFU |
author_sort | YAO, WU |
collection | PubMed |
description | To investigate the effects of silica on circulating fibrocytes (cFbs), the present study established a primary culture model of rat alveolar macrophages and cFbs in vitro. Macrophages were treated with free silica, and their supernatant was used to stimulate cFbs. The mRNA expression levels of collagen I, collagen III and α-smooth muscle actin (SMA) in cFbs were analyzed by reverse transcription-quantitative polymerase chain reaction. The intracellular and extracellular protein expression levels of collagen I, collagen III and α-SMA were detected by ELISA and immunofluorescence staining. The results indicated that in the cell model, the free silica effectively increased the protein and mRNA expression levels of collagen-I, collagen-III and α-SMA. The free silica significantly promoted the transdifferentiation of cFbs into myofibroblasts in a dose-and time-dependent manner. |
format | Online Article Text |
id | pubmed-4581811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-45818112015-11-30 Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro YAO, WU LIU, SUNA LI, JU HAO, CHANGFU Mol Med Rep Articles To investigate the effects of silica on circulating fibrocytes (cFbs), the present study established a primary culture model of rat alveolar macrophages and cFbs in vitro. Macrophages were treated with free silica, and their supernatant was used to stimulate cFbs. The mRNA expression levels of collagen I, collagen III and α-smooth muscle actin (SMA) in cFbs were analyzed by reverse transcription-quantitative polymerase chain reaction. The intracellular and extracellular protein expression levels of collagen I, collagen III and α-SMA were detected by ELISA and immunofluorescence staining. The results indicated that in the cell model, the free silica effectively increased the protein and mRNA expression levels of collagen-I, collagen-III and α-SMA. The free silica significantly promoted the transdifferentiation of cFbs into myofibroblasts in a dose-and time-dependent manner. D.A. Spandidos 2015-10 2015-08-11 /pmc/articles/PMC4581811/ /pubmed/26299717 http://dx.doi.org/10.3892/mmr.2015.4212 Text en Copyright: © Yao. https://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of a Creative Commons Attribution License |
spellingShingle | Articles YAO, WU LIU, SUNA LI, JU HAO, CHANGFU Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro |
title | Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro |
title_full | Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro |
title_fullStr | Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro |
title_full_unstemmed | Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro |
title_short | Silica promotes the transdifferentiation of rat circulating fibrocytes in vitro |
title_sort | silica promotes the transdifferentiation of rat circulating fibrocytes in vitro |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581811/ https://www.ncbi.nlm.nih.gov/pubmed/26299717 http://dx.doi.org/10.3892/mmr.2015.4212 |
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