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Pericytes display increased CCN2 expression upon culturing

By providing a source of α-smooth muscle actin (α-SMA)-expressing myofibroblasts, microvascular pericytes contribute to the matrix remodeling that occurs during tissue repair. However, the extent to which pericytes may contribute to the fibroblast phenotype post-repair is unknown. In this report, we...

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Detalles Bibliográficos
Autores principales: Shiwen, Xu, Rajkumar, Vineeth, Denton, Christopher P., Leask, Andrew, Abraham, David J.
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686756/
https://www.ncbi.nlm.nih.gov/pubmed/19384472
http://dx.doi.org/10.1007/s12079-009-0053-7
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author Shiwen, Xu
Rajkumar, Vineeth
Denton, Christopher P.
Leask, Andrew
Abraham, David J.
author_facet Shiwen, Xu
Rajkumar, Vineeth
Denton, Christopher P.
Leask, Andrew
Abraham, David J.
author_sort Shiwen, Xu
collection PubMed
description By providing a source of α-smooth muscle actin (α-SMA)-expressing myofibroblasts, microvascular pericytes contribute to the matrix remodeling that occurs during tissue repair. However, the extent to which pericytes may contribute to the fibroblast phenotype post-repair is unknown. In this report, we test whether pericytes isolated from human placenta can in principle become fibroblast-like. Pericytes were cultured in vitro for 11 passages. The Affymetrix mRNA expression profile of passage 2 and passage 11 pericytes was compared. The expression of type I collagen, thrombospondin and fibronectin mRNAs was induced by passaging pericytes in culture. This induction of a fibroblast phenotype was paralleled by induction of connective tissue growth factor (CTGF/CCN2) and type I collagen protein expression and the fibroblast marker ASO2. These results indicate that, in principle, pericytes have the capacity to become fibroblast-like and that pericytes may contribute to the population of fibroblasts in a healed wound.
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spelling pubmed-26867562009-06-08 Pericytes display increased CCN2 expression upon culturing Shiwen, Xu Rajkumar, Vineeth Denton, Christopher P. Leask, Andrew Abraham, David J. J Cell Commun Signal Research Article By providing a source of α-smooth muscle actin (α-SMA)-expressing myofibroblasts, microvascular pericytes contribute to the matrix remodeling that occurs during tissue repair. However, the extent to which pericytes may contribute to the fibroblast phenotype post-repair is unknown. In this report, we test whether pericytes isolated from human placenta can in principle become fibroblast-like. Pericytes were cultured in vitro for 11 passages. The Affymetrix mRNA expression profile of passage 2 and passage 11 pericytes was compared. The expression of type I collagen, thrombospondin and fibronectin mRNAs was induced by passaging pericytes in culture. This induction of a fibroblast phenotype was paralleled by induction of connective tissue growth factor (CTGF/CCN2) and type I collagen protein expression and the fibroblast marker ASO2. These results indicate that, in principle, pericytes have the capacity to become fibroblast-like and that pericytes may contribute to the population of fibroblasts in a healed wound. Springer Netherlands 2009-04-22 2009-03 /pmc/articles/PMC2686756/ /pubmed/19384472 http://dx.doi.org/10.1007/s12079-009-0053-7 Text en © The Author(s) 2009
spellingShingle Research Article
Shiwen, Xu
Rajkumar, Vineeth
Denton, Christopher P.
Leask, Andrew
Abraham, David J.
Pericytes display increased CCN2 expression upon culturing
title Pericytes display increased CCN2 expression upon culturing
title_full Pericytes display increased CCN2 expression upon culturing
title_fullStr Pericytes display increased CCN2 expression upon culturing
title_full_unstemmed Pericytes display increased CCN2 expression upon culturing
title_short Pericytes display increased CCN2 expression upon culturing
title_sort pericytes display increased ccn2 expression upon culturing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686756/
https://www.ncbi.nlm.nih.gov/pubmed/19384472
http://dx.doi.org/10.1007/s12079-009-0053-7
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AT rajkumarvineeth pericytesdisplayincreasedccn2expressionuponculturing
AT dentonchristopherp pericytesdisplayincreasedccn2expressionuponculturing
AT leaskandrew pericytesdisplayincreasedccn2expressionuponculturing
AT abrahamdavidj pericytesdisplayincreasedccn2expressionuponculturing