Physical plasma therapy accelerates wound re‐epithelialisation and enhances extracellular matrix formation in cutaneous skin grafts
Skin grafting is a surgical method of cutaneous reconstruction, which provides volumetric replacement in wounds unable to heal by primary intention. Clinically, full‐thickness skin grafts (FTSGs) are placed in aesthetically sensitive and mechanically demanding areas such as the hands, face, and neck...
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Veröffentlicht in: | The Journal of pathology 2020-12, Vol.252 (4), p.451-464 |
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creator | Frescaline, Nadira Duchesne, Constance Favier, Maryline Onifarasoaniaina, Rachel Guilbert, Thomas Uzan, Georges Banzet, Sébastien Rousseau, Antoine Lataillade, Jean‐Jacques |
description | Skin grafting is a surgical method of cutaneous reconstruction, which provides volumetric replacement in wounds unable to heal by primary intention. Clinically, full‐thickness skin grafts (FTSGs) are placed in aesthetically sensitive and mechanically demanding areas such as the hands, face, and neck. Complete or partial graft failure is the primary complication associated with this surgical procedure. Strategies aimed at improving the rate of skin graft integration will reduce the incidence of graft failure. Cold atmospheric plasma (CAP) is an emerging technology offering innovative clinical applications. The aim of this study was to test the therapeutic potential of CAP to improve wound healing and skin graft integration into the recipient site. In vitro models that mimic wound healing were used to investigate the ability of CAP to enhance cellular migration, a key factor in cutaneous tissue repair. We demonstrated that CAP enhanced the migration of epidermal keratinocytes and dermal fibroblasts. This increased cellular migration was possibly induced by the low dose of reactive oxygen and nitrogen species produced by CAP. Using a mouse model of burn wound reconstructed with a full‐thickness skin graft, we showed that wounds treated with CAP healed faster than did control wounds. Immunohistochemical wound analysis showed that CAP treatment enhanced the expression of the dermal–epidermal junction components, which are vital for successful skin graft integration. CAP treatment was characterised by increased levels of Tgfbr1 mRNA and collagen I protein in vivo, suggesting enhanced wound maturity and extracellular matrix deposition. Mechanistically, we show that CAP induced the activation of the canonical SMAD‐dependent TGF‐β1 pathway in primary human dermal fibroblasts, which may explain the increased collagen I synthesis in vitro. These studies revealed that CAP improved wound repair and skin graft integration via mechanisms involving extracellular matrix formation. CAP offers a novel approach for treating cutaneous wounds and skin grafts. © 2020 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/path.5546 |
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Clinically, full‐thickness skin grafts (FTSGs) are placed in aesthetically sensitive and mechanically demanding areas such as the hands, face, and neck. Complete or partial graft failure is the primary complication associated with this surgical procedure. Strategies aimed at improving the rate of skin graft integration will reduce the incidence of graft failure. Cold atmospheric plasma (CAP) is an emerging technology offering innovative clinical applications. The aim of this study was to test the therapeutic potential of CAP to improve wound healing and skin graft integration into the recipient site. In vitro models that mimic wound healing were used to investigate the ability of CAP to enhance cellular migration, a key factor in cutaneous tissue repair. We demonstrated that CAP enhanced the migration of epidermal keratinocytes and dermal fibroblasts. This increased cellular migration was possibly induced by the low dose of reactive oxygen and nitrogen species produced by CAP. Using a mouse model of burn wound reconstructed with a full‐thickness skin graft, we showed that wounds treated with CAP healed faster than did control wounds. Immunohistochemical wound analysis showed that CAP treatment enhanced the expression of the dermal–epidermal junction components, which are vital for successful skin graft integration. CAP treatment was characterised by increased levels of Tgfbr1 mRNA and collagen I protein in vivo, suggesting enhanced wound maturity and extracellular matrix deposition. Mechanistically, we show that CAP induced the activation of the canonical SMAD‐dependent TGF‐β1 pathway in primary human dermal fibroblasts, which may explain the increased collagen I synthesis in vitro. These studies revealed that CAP improved wound repair and skin graft integration via mechanisms involving extracellular matrix formation. CAP offers a novel approach for treating cutaneous wounds and skin grafts. © 2020 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</description><identifier>ISSN: 0022-3417</identifier><identifier>EISSN: 1096-9896</identifier><identifier>DOI: 10.1002/path.5546</identifier><identifier>PMID: 32918753</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Animal models ; Animals ; Burns - physiopathology ; Burns - surgery ; Cell Movement - physiology ; Cell Proliferation ; cold atmospheric plasma ; collagen ; Collagen (type I) ; dermal–epidermal junction ; Extracellular matrix ; Extracellular Matrix - physiology ; Fibroblasts ; full‐thickness burn wound ; Graft rejection ; Grafts ; Integration ; Keratinocytes ; Keratinocytes - physiology ; Life Sciences ; Life Sciences & Biomedicine ; Mice ; Models, Animal ; mRNA ; Oncology ; Pathology ; Plasma Gases - therapeutic use ; Plastic surgery ; Re-Epithelialization - physiology ; Reactive nitrogen species ; Reactive oxygen species ; Science & Technology ; Skin ; Skin & tissue grafts ; Skin Physiological Phenomena ; Skin Transplantation - methods ; SMAD ; Smad protein ; TGF‐β ; Transforming growth factor-b1 ; Treatment Outcome ; Wound healing ; Wound Healing - physiology</subject><ispartof>The Journal of pathology, 2020-12, Vol.252 (4), p.451-464</ispartof><rights>2020 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</rights><rights>Copyright © 2020 Pathological Society of Great Britain and Ireland</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>22</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000578821500001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c4226-cda9adada2a68ee27a442f68c5f5fc210c124fe4f79ded4c8449a910fabccdd23</citedby><cites>FETCH-LOGICAL-c4226-cda9adada2a68ee27a442f68c5f5fc210c124fe4f79ded4c8449a910fabccdd23</cites><orcidid>0000-0002-2673-8025 ; 0000-0003-0785-0019 ; 0000-0002-0178-5386 ; 0000-0001-5069-0730 ; 0000-0002-8965-5307</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpath.5546$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpath.5546$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,315,782,786,887,1419,27931,27932,28255,45581,45582</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32918753$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.sorbonne-universite.fr/hal-02986638$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Frescaline, Nadira</creatorcontrib><creatorcontrib>Duchesne, Constance</creatorcontrib><creatorcontrib>Favier, Maryline</creatorcontrib><creatorcontrib>Onifarasoaniaina, Rachel</creatorcontrib><creatorcontrib>Guilbert, Thomas</creatorcontrib><creatorcontrib>Uzan, Georges</creatorcontrib><creatorcontrib>Banzet, Sébastien</creatorcontrib><creatorcontrib>Rousseau, Antoine</creatorcontrib><creatorcontrib>Lataillade, Jean‐Jacques</creatorcontrib><title>Physical plasma therapy accelerates wound re‐epithelialisation and enhances extracellular matrix formation in cutaneous skin grafts</title><title>The Journal of pathology</title><addtitle>J PATHOL</addtitle><addtitle>J Pathol</addtitle><description>Skin grafting is a surgical method of cutaneous reconstruction, which provides volumetric replacement in wounds unable to heal by primary intention. Clinically, full‐thickness skin grafts (FTSGs) are placed in aesthetically sensitive and mechanically demanding areas such as the hands, face, and neck. Complete or partial graft failure is the primary complication associated with this surgical procedure. Strategies aimed at improving the rate of skin graft integration will reduce the incidence of graft failure. Cold atmospheric plasma (CAP) is an emerging technology offering innovative clinical applications. The aim of this study was to test the therapeutic potential of CAP to improve wound healing and skin graft integration into the recipient site. In vitro models that mimic wound healing were used to investigate the ability of CAP to enhance cellular migration, a key factor in cutaneous tissue repair. We demonstrated that CAP enhanced the migration of epidermal keratinocytes and dermal fibroblasts. This increased cellular migration was possibly induced by the low dose of reactive oxygen and nitrogen species produced by CAP. Using a mouse model of burn wound reconstructed with a full‐thickness skin graft, we showed that wounds treated with CAP healed faster than did control wounds. Immunohistochemical wound analysis showed that CAP treatment enhanced the expression of the dermal–epidermal junction components, which are vital for successful skin graft integration. CAP treatment was characterised by increased levels of Tgfbr1 mRNA and collagen I protein in vivo, suggesting enhanced wound maturity and extracellular matrix deposition. Mechanistically, we show that CAP induced the activation of the canonical SMAD‐dependent TGF‐β1 pathway in primary human dermal fibroblasts, which may explain the increased collagen I synthesis in vitro. These studies revealed that CAP improved wound repair and skin graft integration via mechanisms involving extracellular matrix formation. CAP offers a novel approach for treating cutaneous wounds and skin grafts. © 2020 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</description><subject>Animal models</subject><subject>Animals</subject><subject>Burns - physiopathology</subject><subject>Burns - surgery</subject><subject>Cell Movement - physiology</subject><subject>Cell Proliferation</subject><subject>cold atmospheric plasma</subject><subject>collagen</subject><subject>Collagen (type I)</subject><subject>dermal–epidermal junction</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - physiology</subject><subject>Fibroblasts</subject><subject>full‐thickness burn wound</subject><subject>Graft rejection</subject><subject>Grafts</subject><subject>Integration</subject><subject>Keratinocytes</subject><subject>Keratinocytes - physiology</subject><subject>Life Sciences</subject><subject>Life Sciences & Biomedicine</subject><subject>Mice</subject><subject>Models, Animal</subject><subject>mRNA</subject><subject>Oncology</subject><subject>Pathology</subject><subject>Plasma Gases - therapeutic use</subject><subject>Plastic surgery</subject><subject>Re-Epithelialization - physiology</subject><subject>Reactive nitrogen species</subject><subject>Reactive oxygen species</subject><subject>Science & Technology</subject><subject>Skin</subject><subject>Skin & tissue grafts</subject><subject>Skin Physiological Phenomena</subject><subject>Skin Transplantation - methods</subject><subject>SMAD</subject><subject>Smad protein</subject><subject>TGF‐β</subject><subject>Transforming growth factor-b1</subject><subject>Treatment Outcome</subject><subject>Wound healing</subject><subject>Wound Healing - physiology</subject><issn>0022-3417</issn><issn>1096-9896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhiMEokvhwB9AlrhQoW1tx07s42pFWaSV6KGco1nHJi7OB7bTdm9cuPMb-SU4zbJISEjIB3_MMzPv-M2ylwSfE4zpxQCxOeecFY-yBcGyWEohi8fZIsXoMmekPMmehXCDMZaS86fZSU4lESXPF9n3q2YfrAKHBgehBRQb7WHYI1BKu3SMOqC7fuxq5PXPbz_0YBPhLDgbINq-Q5BCumugU4nU99FDSnSjA49aiN7eI9P7dmZth9QYodP9GFD4kq6fPZgYnmdPDLigXxz20-zT5bvr9Wa5_fj-w3q1XSpGabFUNUio06JQCK1pCYxRUwjFDTeKEqwIZUYzU8pa10wJxiRIgg3slKprmp9mZ3PdBlw1eNuC31c92Gqz2lbTG6ZSFEUubkli38zs4Puvow6xam2YRpvlVzT1piTHJE_o67_Qm370XZokUQXhZSl48ae58n0IXpujAoKrycdq8rGafEzsq0PFcdfq-kj-Ni4Bb2fgTu96E5TV6f-PWHKal0JQwtMJT7OI_6fXNj64tU6ux5R6cUi1Tu__Lbm6Wl1vHrT_As9pzNM</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Frescaline, Nadira</creator><creator>Duchesne, Constance</creator><creator>Favier, Maryline</creator><creator>Onifarasoaniaina, Rachel</creator><creator>Guilbert, Thomas</creator><creator>Uzan, Georges</creator><creator>Banzet, Sébastien</creator><creator>Rousseau, Antoine</creator><creator>Lataillade, Jean‐Jacques</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-2673-8025</orcidid><orcidid>https://orcid.org/0000-0003-0785-0019</orcidid><orcidid>https://orcid.org/0000-0002-0178-5386</orcidid><orcidid>https://orcid.org/0000-0001-5069-0730</orcidid><orcidid>https://orcid.org/0000-0002-8965-5307</orcidid></search><sort><creationdate>202012</creationdate><title>Physical plasma therapy accelerates wound re‐epithelialisation and enhances extracellular matrix formation in cutaneous skin grafts</title><author>Frescaline, Nadira ; Duchesne, Constance ; Favier, Maryline ; Onifarasoaniaina, Rachel ; Guilbert, Thomas ; Uzan, Georges ; Banzet, Sébastien ; Rousseau, Antoine ; Lataillade, Jean‐Jacques</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4226-cda9adada2a68ee27a442f68c5f5fc210c124fe4f79ded4c8449a910fabccdd23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Burns - physiopathology</topic><topic>Burns - surgery</topic><topic>Cell Movement - physiology</topic><topic>Cell Proliferation</topic><topic>cold atmospheric plasma</topic><topic>collagen</topic><topic>Collagen (type I)</topic><topic>dermal–epidermal junction</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix - physiology</topic><topic>Fibroblasts</topic><topic>full‐thickness burn wound</topic><topic>Graft rejection</topic><topic>Grafts</topic><topic>Integration</topic><topic>Keratinocytes</topic><topic>Keratinocytes - physiology</topic><topic>Life Sciences</topic><topic>Life Sciences & Biomedicine</topic><topic>Mice</topic><topic>Models, Animal</topic><topic>mRNA</topic><topic>Oncology</topic><topic>Pathology</topic><topic>Plasma Gases - therapeutic use</topic><topic>Plastic surgery</topic><topic>Re-Epithelialization - physiology</topic><topic>Reactive nitrogen species</topic><topic>Reactive oxygen species</topic><topic>Science & Technology</topic><topic>Skin</topic><topic>Skin & tissue grafts</topic><topic>Skin Physiological Phenomena</topic><topic>Skin Transplantation - methods</topic><topic>SMAD</topic><topic>Smad protein</topic><topic>TGF‐β</topic><topic>Transforming growth factor-b1</topic><topic>Treatment Outcome</topic><topic>Wound healing</topic><topic>Wound Healing - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frescaline, Nadira</creatorcontrib><creatorcontrib>Duchesne, Constance</creatorcontrib><creatorcontrib>Favier, Maryline</creatorcontrib><creatorcontrib>Onifarasoaniaina, Rachel</creatorcontrib><creatorcontrib>Guilbert, Thomas</creatorcontrib><creatorcontrib>Uzan, Georges</creatorcontrib><creatorcontrib>Banzet, Sébastien</creatorcontrib><creatorcontrib>Rousseau, Antoine</creatorcontrib><creatorcontrib>Lataillade, Jean‐Jacques</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>The Journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frescaline, Nadira</au><au>Duchesne, Constance</au><au>Favier, Maryline</au><au>Onifarasoaniaina, Rachel</au><au>Guilbert, Thomas</au><au>Uzan, Georges</au><au>Banzet, Sébastien</au><au>Rousseau, Antoine</au><au>Lataillade, Jean‐Jacques</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical plasma therapy accelerates wound re‐epithelialisation and enhances extracellular matrix formation in cutaneous skin grafts</atitle><jtitle>The Journal of pathology</jtitle><stitle>J PATHOL</stitle><addtitle>J Pathol</addtitle><date>2020-12</date><risdate>2020</risdate><volume>252</volume><issue>4</issue><spage>451</spage><epage>464</epage><pages>451-464</pages><issn>0022-3417</issn><eissn>1096-9896</eissn><abstract>Skin grafting is a surgical method of cutaneous reconstruction, which provides volumetric replacement in wounds unable to heal by primary intention. Clinically, full‐thickness skin grafts (FTSGs) are placed in aesthetically sensitive and mechanically demanding areas such as the hands, face, and neck. Complete or partial graft failure is the primary complication associated with this surgical procedure. Strategies aimed at improving the rate of skin graft integration will reduce the incidence of graft failure. Cold atmospheric plasma (CAP) is an emerging technology offering innovative clinical applications. The aim of this study was to test the therapeutic potential of CAP to improve wound healing and skin graft integration into the recipient site. In vitro models that mimic wound healing were used to investigate the ability of CAP to enhance cellular migration, a key factor in cutaneous tissue repair. We demonstrated that CAP enhanced the migration of epidermal keratinocytes and dermal fibroblasts. This increased cellular migration was possibly induced by the low dose of reactive oxygen and nitrogen species produced by CAP. Using a mouse model of burn wound reconstructed with a full‐thickness skin graft, we showed that wounds treated with CAP healed faster than did control wounds. Immunohistochemical wound analysis showed that CAP treatment enhanced the expression of the dermal–epidermal junction components, which are vital for successful skin graft integration. CAP treatment was characterised by increased levels of Tgfbr1 mRNA and collagen I protein in vivo, suggesting enhanced wound maturity and extracellular matrix deposition. Mechanistically, we show that CAP induced the activation of the canonical SMAD‐dependent TGF‐β1 pathway in primary human dermal fibroblasts, which may explain the increased collagen I synthesis in vitro. These studies revealed that CAP improved wound repair and skin graft integration via mechanisms involving extracellular matrix formation. CAP offers a novel approach for treating cutaneous wounds and skin grafts. © 2020 The Pathological Society of Great Britain and Ireland. 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subjects | Animal models Animals Burns - physiopathology Burns - surgery Cell Movement - physiology Cell Proliferation cold atmospheric plasma collagen Collagen (type I) dermal–epidermal junction Extracellular matrix Extracellular Matrix - physiology Fibroblasts full‐thickness burn wound Graft rejection Grafts Integration Keratinocytes Keratinocytes - physiology Life Sciences Life Sciences & Biomedicine Mice Models, Animal mRNA Oncology Pathology Plasma Gases - therapeutic use Plastic surgery Re-Epithelialization - physiology Reactive nitrogen species Reactive oxygen species Science & Technology Skin Skin & tissue grafts Skin Physiological Phenomena Skin Transplantation - methods SMAD Smad protein TGF‐β Transforming growth factor-b1 Treatment Outcome Wound healing Wound Healing - physiology |
title | Physical plasma therapy accelerates wound re‐epithelialisation and enhances extracellular matrix formation in cutaneous skin grafts |
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