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Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure

Stromal vascular fraction (SVF) cells, and the adipose-derived mesenchymal stem cells they contain, have shown enhanced wound healing in vitro and in vivo, yet their clinical application has been limited. In this regard, understanding the mechanisms that govern SVF-enhanced wound healing would impro...

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Autores principales: Balko, Stefan, Kerr, Evan, Buchel, Ed, Logsetty, Sarvesh, Raouf, Afshin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510163/
https://www.ncbi.nlm.nih.gov/pubmed/37726799
http://dx.doi.org/10.1186/s13287-023-03488-0
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author Balko, Stefan
Kerr, Evan
Buchel, Ed
Logsetty, Sarvesh
Raouf, Afshin
author_facet Balko, Stefan
Kerr, Evan
Buchel, Ed
Logsetty, Sarvesh
Raouf, Afshin
author_sort Balko, Stefan
collection PubMed
description Stromal vascular fraction (SVF) cells, and the adipose-derived mesenchymal stem cells they contain, have shown enhanced wound healing in vitro and in vivo, yet their clinical application has been limited. In this regard, understanding the mechanisms that govern SVF-enhanced wound healing would improve their application in the clinic. Here, we show that the SVF cells and keratinocytes engage in a paracrine crosstalk during wound closure, which results in a new cytokine profile that is distinct from the cytokines regularly secreted by either cell type on their own. We identify 11 cytokines, 5 of which are not regularly secreted by the SVF cells, whose expressions are significantly increased during wound closure by the keratinocytes. This new cytokine profile could be used to accelerate wound closure and initiate re-epithelialization without the need to obtain the SVF cells from the patient. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03488-0.
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spelling pubmed-105101632023-09-21 Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure Balko, Stefan Kerr, Evan Buchel, Ed Logsetty, Sarvesh Raouf, Afshin Stem Cell Res Ther Short Report Stromal vascular fraction (SVF) cells, and the adipose-derived mesenchymal stem cells they contain, have shown enhanced wound healing in vitro and in vivo, yet their clinical application has been limited. In this regard, understanding the mechanisms that govern SVF-enhanced wound healing would improve their application in the clinic. Here, we show that the SVF cells and keratinocytes engage in a paracrine crosstalk during wound closure, which results in a new cytokine profile that is distinct from the cytokines regularly secreted by either cell type on their own. We identify 11 cytokines, 5 of which are not regularly secreted by the SVF cells, whose expressions are significantly increased during wound closure by the keratinocytes. This new cytokine profile could be used to accelerate wound closure and initiate re-epithelialization without the need to obtain the SVF cells from the patient. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03488-0. BioMed Central 2023-09-19 /pmc/articles/PMC10510163/ /pubmed/37726799 http://dx.doi.org/10.1186/s13287-023-03488-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Short Report
Balko, Stefan
Kerr, Evan
Buchel, Ed
Logsetty, Sarvesh
Raouf, Afshin
Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure
title Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure
title_full Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure
title_fullStr Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure
title_full_unstemmed Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure
title_short Paracrine signalling between keratinocytes and SVF cells results in a new secreted cytokine profile during wound closure
title_sort paracrine signalling between keratinocytes and svf cells results in a new secreted cytokine profile during wound closure
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510163/
https://www.ncbi.nlm.nih.gov/pubmed/37726799
http://dx.doi.org/10.1186/s13287-023-03488-0
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