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Atmospheric-Pressure Cold Plasma Induces Transcriptional Changes in Ex Vivo Human Corneas

Academic Article
Publication Date:
2015
abstract:
Background: Atmospheric pressure cold plasma (APCP) might be considered a novel tool for tissue disinfection in medicine since the active chemical species produced by low plasma doses, generated by ionizing helium gas in air, induces reactive oxygen species (ROS) that kill microorganisms without substantially affecting human cells. Objectives: In this study, we evaluated morphological and functional changes in human corneas exposed for 2 minutes (min) to APCP and tested if the antioxidant n-acetyl l-cysteine (NAC) was able to inhibit or prevent damage and cell death. Results: Immunohistochemistry and western blotting analyses of corneal tissues collected at 6 hours (h) post-APCP treatment demonstrated no morphological tissue changes, but a transient increased expression of OGG1 glycosylase that returned to control levels in 24 h. Transcriptome sequencing and quantitative real time PCR performed on different corneas revealed in the treated corneas many differentially expressed genes: namely, 256 and 304 genes showing expression changes greater than ± 2 folds in the absence and presence of NAC, respectively. At 6 h post-treatment, the most over-expressed gene categories suggested an active or enhanced cell functioning, with only a minority of genes specifically concerning oxidative DNA damage and repair showing slight over-expression values (<2 folds). Moreover, time-related expression analysis of eight genes up-regulated in the APCP-treated corneas overall demonstrated the return to control expression levels after 24 h. Conclusions: These findings of transient oxidative stress accompanied by wide-range transcriptome adjustments support the further development of APCP as an ocular disinfectant.
Iris type:
01.01 Articolo in rivista
Keywords:
acetylcysteine; glycosyltransferase; protein OGG1; unclassified drug; aged; Article; atmospheric pressure cold plasma; cell death; cell function; cell protection; controlled study; cornea; disinfection; DNA damage; DNA repair; ex vivo study; functional morphology; gene expression regulation; gene overexpression; gene sequence; genetic transcription; human; human tissue; immunohistochemistry; oxidative stress; plasma; quantitative analysis; real time polymerase chain reaction; tissue structure; upregulation; Western blotting
List of contributors:
Martines, Emilio; Zuin, Matteo
Authors of the University:
ZUIN MATTEO
Handle:
https://iris.cnr.it/handle/20.500.14243/296146
Published in:
PLOS ONE
Journal
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URL

http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0133173
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