Effect of Cold Plasma on Cell Viability and Collagen Synthesis in Cultured Murine Fibroblasts

An argon atmospheric pressure plasma jet was employed to treat L929 murine fibroblasts cultured in vitro.Experimental results showed that,compared with the control cells,the treatment of fibroblasts with 15 s of plasma led to a significant increase of cell viability and collagen synthesis,while the...

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Published inPlasma science & technology Vol. 18; no. 4; pp. 353 - 359
Main Author 石兴民 蔡晶芬 许桂敏 任鸿斌 陈思乐 常正实 刘进仁 黄崇亚 张冠军 吴喜利
Format Journal Article
LanguageEnglish
Published 01.04.2016
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ISSN1009-0630
DOI10.1088/1009-0630/18/4/04

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Summary:An argon atmospheric pressure plasma jet was employed to treat L929 murine fibroblasts cultured in vitro.Experimental results showed that,compared with the control cells,the treatment of fibroblasts with 15 s of plasma led to a significant increase of cell viability and collagen synthesis,while the treatment of 25 s plasma resulted in a remarkable decrease.Exploration of related mechanisms suggested that cold plasma could up-regulate Cyclin D1 gene expression and down-regulate p27 gene expression at a low dose,while it could down-regulate Cyclin D1 expression and up-regulate p27 expression at a higher dose,thus altering the cell cycle progression,and then affecting cell viability and collagen synthesis of fibroblasts.
Bibliography:cold plasma cell viability collagen synthesis fibroblasts
An argon atmospheric pressure plasma jet was employed to treat L929 murine fibroblasts cultured in vitro.Experimental results showed that,compared with the control cells,the treatment of fibroblasts with 15 s of plasma led to a significant increase of cell viability and collagen synthesis,while the treatment of 25 s plasma resulted in a remarkable decrease.Exploration of related mechanisms suggested that cold plasma could up-regulate Cyclin D1 gene expression and down-regulate p27 gene expression at a low dose,while it could down-regulate Cyclin D1 expression and up-regulate p27 expression at a higher dose,thus altering the cell cycle progression,and then affecting cell viability and collagen synthesis of fibroblasts.
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ISSN:1009-0630
DOI:10.1088/1009-0630/18/4/04