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Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts

Clinically, wounds on the face tend to heal with less scarring than those on the trunk, but the causes of this difference have not been clarified. Fibroblasts obtained from different parts of the body are known to show different properties. To investigate whether the characteristic properties of fac...

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Autores principales: Kurita, Masakazu, Okazaki, Mutsumi, Kaminishi-Tanikawa, Akiko, Niikura, Mamoru, Takushima, Akihiko, Harii, Kiyonori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483065/
https://www.ncbi.nlm.nih.gov/pubmed/22260504
http://dx.doi.org/10.3109/03008207.2012.657309
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author Kurita, Masakazu
Okazaki, Mutsumi
Kaminishi-Tanikawa, Akiko
Niikura, Mamoru
Takushima, Akihiko
Harii, Kiyonori
author_facet Kurita, Masakazu
Okazaki, Mutsumi
Kaminishi-Tanikawa, Akiko
Niikura, Mamoru
Takushima, Akihiko
Harii, Kiyonori
author_sort Kurita, Masakazu
collection PubMed
description Clinically, wounds on the face tend to heal with less scarring than those on the trunk, but the causes of this difference have not been clarified. Fibroblasts obtained from different parts of the body are known to show different properties. To investigate whether the characteristic properties of facial and trunk wound healing are caused by differences in local fibroblasts, we comparatively analyzed the functional properties of superficial and deep dermal fibroblasts obtained from the facial and trunk skin of seven individuals, with an emphasis on tendency for fibrosis. Proliferation kinetics and mRNA and protein expression of 11 fibrosis-associated factors were investigated. The proliferation kinetics of facial and trunk fibroblasts were identical, but the expression and production levels of profibrotic factors, such as extracellular matrix, transforming growth factor-β1, and connective tissue growth factor mRNA, were lower in facial fibroblasts when compared with trunk fibro-blasts, while the expression of antifibrotic factors, such as collagenase, basic fibroblast growth factor, and hepatocyte growth factor, showed no clear trends. The differences in functional properties of facial and trunk dermal fibroblasts were consistent with the clinical tendencies of healing of facial and trunk wounds. Thus, the differences between facial and trunk scarring are at least partly related to the intrinsic nature of the local dermal fibroblasts.
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spelling pubmed-34830652012-11-01 Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts Kurita, Masakazu Okazaki, Mutsumi Kaminishi-Tanikawa, Akiko Niikura, Mamoru Takushima, Akihiko Harii, Kiyonori Connect Tissue Res Review Article Clinically, wounds on the face tend to heal with less scarring than those on the trunk, but the causes of this difference have not been clarified. Fibroblasts obtained from different parts of the body are known to show different properties. To investigate whether the characteristic properties of facial and trunk wound healing are caused by differences in local fibroblasts, we comparatively analyzed the functional properties of superficial and deep dermal fibroblasts obtained from the facial and trunk skin of seven individuals, with an emphasis on tendency for fibrosis. Proliferation kinetics and mRNA and protein expression of 11 fibrosis-associated factors were investigated. The proliferation kinetics of facial and trunk fibroblasts were identical, but the expression and production levels of profibrotic factors, such as extracellular matrix, transforming growth factor-β1, and connective tissue growth factor mRNA, were lower in facial fibroblasts when compared with trunk fibro-blasts, while the expression of antifibrotic factors, such as collagenase, basic fibroblast growth factor, and hepatocyte growth factor, showed no clear trends. The differences in functional properties of facial and trunk dermal fibroblasts were consistent with the clinical tendencies of healing of facial and trunk wounds. Thus, the differences between facial and trunk scarring are at least partly related to the intrinsic nature of the local dermal fibroblasts. Informa Healthcare 2012-10 2012-07-24 /pmc/articles/PMC3483065/ /pubmed/22260504 http://dx.doi.org/10.3109/03008207.2012.657309 Text en © 2012 Informa Healthcare USA, Inc. http://creativecommons.org/licenses/by/2.0/ This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Informa Healthcare journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kurita, Masakazu
Okazaki, Mutsumi
Kaminishi-Tanikawa, Akiko
Niikura, Mamoru
Takushima, Akihiko
Harii, Kiyonori
Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts
title Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts
title_full Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts
title_fullStr Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts
title_full_unstemmed Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts
title_short Differential Expression of Wound Fibrotic Factors between Facial and Trunk Dermal Fibroblasts
title_sort differential expression of wound fibrotic factors between facial and trunk dermal fibroblasts
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483065/
https://www.ncbi.nlm.nih.gov/pubmed/22260504
http://dx.doi.org/10.3109/03008207.2012.657309
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