gms | German Medical Science

86th Annual Meeting of the German Society of Oto-Rhino-Laryngology, Head and Neck Surgery

German Society of Oto-Rhino-Laryngology, Head and Neck Surgery

13.05. - 16.05.2015, Berlin

Stimulation of airway epithelial cell proliferation and bacterial decontamination mediated by atmospheric pressure nonthermal plasma

Meeting Abstract

  • corresponding author Christian Scharf - HNO-Klinik Greifswald, Greifswald
  • Philipp Emicke - HNO-Klinik Greifswald, Greifswald
  • Achim Beule - HNO-Klinik Greifswald, Greifswald
  • Katrin Darm - HNO-Klinik Greifswald, Greifswald
  • Georg Daeschlein - Dermatologie Greifswald, Greifswald
  • Klaus-Dieter Weltmann - INP Greifswald, Greifswald
  • Werner Hosemann - HNO-Klinik Greifswald, Greifswald

Deutsche Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie. 86. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie. Berlin, 13.-16.05.2015. Düsseldorf: German Medical Science GMS Publishing House; 2015. Doc15hnod624

doi: 10.3205/15hnod624, urn:nbn:de:0183-15hnod6249

Published: March 26, 2015

© 2015 Scharf et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License. You are free: to Share - to copy, distribute and transmit the work, provided the original author and source are credited. See license information at http://creativecommons.org/licenses/by-nc-nd/3.0/.


Outline

Text

Introduction: Development of atmospheric pressure non-thermal plasma (APP) opened a wide field of possible applications in medicine. In previous studies, APP achieved sterilization and improved wound healing. In order to evaluate in-vitro the molecular response to plasma treatment in the human airway, proteome analysis of S9 epithelial cell lines as model for upper epithelial cells and clinical isolates of S. aureus strains as model for the physiologic flora were performed.

Methods & Results: Comparison between plasma-treated human epithelial cells and the corresponding untreated controls indicated obvious differences in proliferation. Moreover, a time-related manner of effects was detected: Up to 60 min after APP, epithelial cells reacted with oxidative stress response, protein modifications, cell protection mechanisms and partly with apoptosis. Surviving human epithelial cells, showed protein regeneration and proliferation after 48 h and 72 h, respectively. In contrast, clinical isolates of S. aureus were sensitive to APP treatment. Also, differences between different bacterial strains were revealed: Next to creation of bacteria-free areolas due to bacterial death, sublethal plasma dosage resulted in dramatic changes in the molecular response of treated bacteria. Proteomic analyses clearly distinguished strain specific molecular responses for S. aureus.

Conclusion: The presented technique opens a hypotheses-free approach for the study of complex host-pathogen interaction as well as for the definition of the outcome of new bacterial treatments. This study suggests APP as a possible adjunction for stimulating regeneration of epithelial cells and simultaneous bacterial decontamination in the human airway.

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