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Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing
Platelets are a recognised potent source of transforming growth factor‐β1 (TGFβ1), a cytokine known to promote wound healing and regeneration by stimulating dermal fibroblast proliferation and extracellular matrix deposition. Platelet lysate has been advocated as a novel personalised therapeutic to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216944/ https://www.ncbi.nlm.nih.gov/pubmed/32068954 http://dx.doi.org/10.1002/term.3022 |
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author | Chong, Deborah L.W. Trinder, Sarah Labelle, Myriam Rodriguez‐Justo, Manuel Hughes, Sian Holmes, Alan M. Scotton, Chris J. Porter, Joanna C. |
author_facet | Chong, Deborah L.W. Trinder, Sarah Labelle, Myriam Rodriguez‐Justo, Manuel Hughes, Sian Holmes, Alan M. Scotton, Chris J. Porter, Joanna C. |
author_sort | Chong, Deborah L.W. |
collection | PubMed |
description | Platelets are a recognised potent source of transforming growth factor‐β1 (TGFβ1), a cytokine known to promote wound healing and regeneration by stimulating dermal fibroblast proliferation and extracellular matrix deposition. Platelet lysate has been advocated as a novel personalised therapeutic to treat persistent wounds, although the precise platelet‐derived growth factors responsible for these beneficial effects have not been fully elucidated. The aim of this study was to investigate the specific role of platelet‐derived TGFβ1 in cutaneous wound healing. Using a transgenic mouse with a targeted deletion of TGFβ1 in megakaryocytes and platelets (TGFβ1(fl/fl).PF4‐Cre), we show for the first time that platelet‐derived TGFβ1 contributes to epidermal and dermal thickening and cellular turnover after excisional skin wounding. In vitro studies demonstrate that human dermal fibroblasts stimulated with platelet lysate containing high levels of platelet‐derived TGFβ1 did not exhibit enhanced collagen deposition or proliferation, suggesting that platelet‐derived TGFβ1 is not a key promoter of these wound healing processes. Interestingly, human keratinocytes displayed enhanced TGFβ1‐driven proliferation in response to platelet lysate, reminiscent of our in vivo findings. In summary, our novel findings define and emphasise an important role of platelet‐derived TGFβ1 in epidermal remodelling and regeneration processes during cutaneous wound healing. |
format | Online Article Text |
id | pubmed-7216944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72169442020-05-13 Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing Chong, Deborah L.W. Trinder, Sarah Labelle, Myriam Rodriguez‐Justo, Manuel Hughes, Sian Holmes, Alan M. Scotton, Chris J. Porter, Joanna C. J Tissue Eng Regen Med Short Communication Platelets are a recognised potent source of transforming growth factor‐β1 (TGFβ1), a cytokine known to promote wound healing and regeneration by stimulating dermal fibroblast proliferation and extracellular matrix deposition. Platelet lysate has been advocated as a novel personalised therapeutic to treat persistent wounds, although the precise platelet‐derived growth factors responsible for these beneficial effects have not been fully elucidated. The aim of this study was to investigate the specific role of platelet‐derived TGFβ1 in cutaneous wound healing. Using a transgenic mouse with a targeted deletion of TGFβ1 in megakaryocytes and platelets (TGFβ1(fl/fl).PF4‐Cre), we show for the first time that platelet‐derived TGFβ1 contributes to epidermal and dermal thickening and cellular turnover after excisional skin wounding. In vitro studies demonstrate that human dermal fibroblasts stimulated with platelet lysate containing high levels of platelet‐derived TGFβ1 did not exhibit enhanced collagen deposition or proliferation, suggesting that platelet‐derived TGFβ1 is not a key promoter of these wound healing processes. Interestingly, human keratinocytes displayed enhanced TGFβ1‐driven proliferation in response to platelet lysate, reminiscent of our in vivo findings. In summary, our novel findings define and emphasise an important role of platelet‐derived TGFβ1 in epidermal remodelling and regeneration processes during cutaneous wound healing. John Wiley and Sons Inc. 2020-03-05 2020-04 /pmc/articles/PMC7216944/ /pubmed/32068954 http://dx.doi.org/10.1002/term.3022 Text en © 2020 The Authors. Journal of Tissue Engineering and Regenerative Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Chong, Deborah L.W. Trinder, Sarah Labelle, Myriam Rodriguez‐Justo, Manuel Hughes, Sian Holmes, Alan M. Scotton, Chris J. Porter, Joanna C. Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing |
title | Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing |
title_full | Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing |
title_fullStr | Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing |
title_full_unstemmed | Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing |
title_short | Platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing |
title_sort | platelet‐derived transforming growth factor‐β1 promotes keratinocyte proliferation in cutaneous wound healing |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216944/ https://www.ncbi.nlm.nih.gov/pubmed/32068954 http://dx.doi.org/10.1002/term.3022 |
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