• Media type: E-Book; Thesis
  • Title: The effect of Cold Atmospheric Plasma (CAP) on the molecular mechanism of wound healing
  • Contributor: Shome, Debarati [Author]; Riedel, Katharina [Degree supervisor]; Lalk, Michael [Degree supervisor]; Emmert, Steffen [Degree supervisor]
  • Corporation: Universität Greifswald
  • Published: Greifswald, 15.06.2020
  • Extent: 1 Online-Ressource (PDF-Datei: 149 Seiten, 4918 Kilobyte); Illustrationen (farbig), Diagramme (teilweise farbig)
  • Language: English; German
  • Identifier:
  • RVK notation: UR 8000 : Plasmaphysik allgemein
    XG 4304 : Dissertation, Habilitationsarbeit
  • Keywords: Plasma > Kaltes Plasma > Atmosphärendruckplasma > Wundheilung > Molekularbiologie
  • Origination:
  • University thesis: Dissertation, Mathematisch-Naturwissenschaftliche Fakultät der Universität Greifswald, 2020
  • Footnote: Literaturverzeichnis: Seite 99-113
    Zusammenfassung in deutscher Sprache
  • Description: Cold Atmospheric Plasma

    Reactive species play an essential role in orchestrating wound healing responses. They act as secondary messengers and drive redox-signaling pathways that are involved in the hemostatic, inflammatory, proliferative and remodeling phases of wound healing. Cold plasma produces a profusion of short- and long-lived redox species that promotes wound healing, however, until today, the knowledge of CAP mediated wound healing remained scarce. In this thesis, CAP mediated wound healing mechanism and their effect on extracellular matrix and adhesion molecules have been investigated. To this end, a keratinocyte cell line (HaCaT), skin fibroblast cell line (GM Fbs) and an in vitro coculture model including both HaCaT and GM Fbs at a 2:1 ratio, were employed to investigate the cross talk between these two skin cell types. We examined the impact of CAP on extracellular matrix proteins and cell adhesion molecules in GM Fbs and observed a significant impact of cold plasma treatment on the expression level of collagen moieties, cell adhesion molecule like integrin, cadherin, versican, MMPs as well as extracellular matrix proteins. Moreover, scratch assays with monocultures of HaCaT, GM Fbs and coculture of these two cell types were performed. We detected that, CAP accelerated the migratory capability of HaCaT cells cocultured with fibroblasts. In fact, compared to HaCaT monoculture, a significant acceleration on cell migration was observed in coculture upon CAP treatment. NAC, a potent ...
  • Access State: Open Access