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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of pathology 2020-12, Vol.252 (4), p.451-464
Hauptverfasser: Frescaline, Nadira, Duchesne, Constance, Favier, Maryline, Onifarasoaniaina, Rachel, Guilbert, Thomas, Uzan, Georges, Banzet, Sébastien, Rousseau, Antoine, Lataillade, Jean‐Jacques
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 464
container_issue 4
container_start_page 451
container_title The Journal of pathology
container_volume 252
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
format Article
fullrecord <record><control><sourceid>proquest_wiley</sourceid><recordid>TN_cdi_wiley_primary_10_1002_path_5546_PATH5546</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2442213013</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4226-cda9adada2a68ee27a442f68c5f5fc210c124fe4f79ded4c8449a910fabccdd23</originalsourceid><addsrcrecordid>eNqNkU1v1DAQhiMEokvhwB9AlrhQoW1tx07s42pFWaSV6KGco1nHJi7OB7bTdm9cuPMb-SU4zbJISEjIB3_MMzPv-M2ylwSfE4zpxQCxOeecFY-yBcGyWEohi8fZIsXoMmekPMmehXCDMZaS86fZSU4lESXPF9n3q2YfrAKHBgehBRQb7WHYI1BKu3SMOqC7fuxq5PXPbz_0YBPhLDgbINq-Q5BCumugU4nU99FDSnSjA49aiN7eI9P7dmZth9QYodP9GFD4kq6fPZgYnmdPDLigXxz20-zT5bvr9Wa5_fj-w3q1XSpGabFUNUio06JQCK1pCYxRUwjFDTeKEqwIZUYzU8pa10wJxiRIgg3slKprmp9mZ3PdBlw1eNuC31c92Gqz2lbTG6ZSFEUubkli38zs4Puvow6xam2YRpvlVzT1piTHJE_o67_Qm370XZokUQXhZSl48ae58n0IXpujAoKrycdq8rGafEzsq0PFcdfq-kj-Ni4Bb2fgTu96E5TV6f-PWHKal0JQwtMJT7OI_6fXNj64tU6ux5R6cUi1Tu__Lbm6Wl1vHrT_As9pzNM</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2461577856</pqid></control><display><type>article</type><title>Physical plasma therapy accelerates wound re‐epithelialisation and enhances extracellular matrix formation in cutaneous skin grafts</title><source>MEDLINE</source><source>Web of Science - Science Citation Index Expanded - 2020&lt;img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" /&gt;</source><source>Wiley Online Library All Journals</source><creator>Frescaline, Nadira ; Duchesne, Constance ; Favier, Maryline ; Onifarasoaniaina, Rachel ; Guilbert, Thomas ; Uzan, Georges ; Banzet, Sébastien ; Rousseau, Antoine ; Lataillade, Jean‐Jacques</creator><creatorcontrib>Frescaline, Nadira ; Duchesne, Constance ; Favier, Maryline ; Onifarasoaniaina, Rachel ; Guilbert, Thomas ; Uzan, Georges ; Banzet, Sébastien ; Rousseau, Antoine ; Lataillade, Jean‐Jacques</creatorcontrib><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 &amp; 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 &amp; 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 &amp; Biomedicine ; Mice ; Models, Animal ; mRNA ; Oncology ; Pathology ; Plasma Gases - therapeutic use ; Plastic surgery ; Re-Epithelialization - physiology ; Reactive nitrogen species ; Reactive oxygen species ; Science &amp; Technology ; Skin ; Skin &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; Technology</subject><subject>Skin</subject><subject>Skin &amp; 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 &amp; 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 &amp; 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 &amp; Technology</topic><topic>Skin</topic><topic>Skin &amp; 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 &amp; 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 &amp; 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. Published by John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>32918753</pmid><doi>10.1002/path.5546</doi><tpages>14</tpages><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><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-3417
ispartof The Journal of pathology, 2020-12, Vol.252 (4), p.451-464
issn 0022-3417
1096-9896
language eng
recordid cdi_wiley_primary_10_1002_path_5546_PATH5546
source MEDLINE; Web of Science - Science Citation Index Expanded - 2020<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; Wiley Online Library All Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-04T23%3A32%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_wiley&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Physical%20plasma%20therapy%20accelerates%20wound%20re%E2%80%90epithelialisation%20and%20enhances%20extracellular%20matrix%20formation%20in%20cutaneous%20skin%20grafts&rft.jtitle=The%20Journal%20of%20pathology&rft.au=Frescaline,%20Nadira&rft.date=2020-12&rft.volume=252&rft.issue=4&rft.spage=451&rft.epage=464&rft.pages=451-464&rft.issn=0022-3417&rft.eissn=1096-9896&rft_id=info:doi/10.1002/path.5546&rft_dat=%3Cproquest_wiley%3E2442213013%3C/proquest_wiley%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2461577856&rft_id=info:pmid/32918753&rfr_iscdi=true