常压冷等离子体诱导活酵母细胞衍生物(LYCD)的特性及其对细胞的保护作用

Ruonan Ma, B. Su, Ying Tian, Qian Zhang, Jing Fang, Jue Zhang, H. Feng, Yongdong Liang
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摘要

只提供摘要形式。在之前的研究中,我们发现在常压冷等离子体处理过程中,酵母细胞的反应需要氧化应激途径。此外,抗氧化超氧化物歧化酶(SOD)基因的过表达对酵母细胞的血浆损伤具有显著的保护作用。这些结果与其他研究小组在哺乳动物细胞上的发现是一致的,从而鼓励我们更多地探索真核细胞在血浆处理下的抗氧化反应,这对指导不久的将来潜在的血浆药物应用的安全性和预防措施有价值。在这项研究中,酵母细胞暴露于亚致死剂量的血浆处理,获得活酵母细胞衍生物(LYCD)。通过分析真核细胞中三个重要的抗氧化系统——超氧化物歧化酶(SOD)系统、过氧化氢酶(CAT)系统和谷胱甘肽(GSH)系统的协同作用,评价血浆诱导LYCD的特点。采用试剂盒检测菌株间SOD、CAT活性、还原性GSH和氧化性GSH的含量,并进行比较。质谱法检测了LYCD的其他重要成分。此外,细胞在UV或H2O2后的LYCD也有保护作用。我们还通过将LYCD应用于不同类型的等离子体细胞,研究了LYCD在等离子体处理后的作用。采用菌落计数法检测大肠杆菌(E. coli)和金黄色葡萄球菌(S. aureus)的存活率,采用XTT法检测酿酒酵母(S. cerevisiae)、人乳腺癌(MCF-7)和人胚胎皮肤成纤维细胞(cc - esf -1)的存活率。结果表明,SOD、CAT活性和LYCD的GSH还原量随血浆处理时间的增加呈线性增加。更有趣的是,从酵母细胞中提取的这三种重要的抗氧化物质可以相互作用。此外,我们观察到血浆诱导的LYCD反过来可以有效地保护各种类型的细胞免受血浆损伤。详细的结果将在会议上讨论。
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Characterization of live yeast cell derivative (LYCD) induced by atmospheric pressure cold plasma and its protective effects on cells
Summary form only given. In previous studies, we have found that during atmospheric pressure cold plasma treatment, oxidative stress pathways are required for yeast cell response. In addition, overexpressions of anti-oxidant superoxide dismutase (SOD) genes can remarkably protective yeast cells from plasma injury. These results are in coincidence with other groups' findings with mammalian cells, thus encouraging us to explore more on the anti-oxidative responses in eukaryotic cells subjected to plasma treatment, which is valuable for guiding the safety and precautionary measures for potential plasma medicine applications in the near future. In this study, the live yeast cell derivative (LYCD) was obtained by yeast cells exposed to sub-lethal doses of plasma treatment. The characteristics of the LYCD induced by plasma were evaluated by analyzing the collaboration of three important anti-oxidative systems in eukaryotic cells, superoxide dismutase (SOD) system, catalase (CAT) system and glutathione (GSH) system. The SOD and CAT activities, as well as reduced GSH and oxidized GSH amount were tested by kits and compared among the strains. And other important compositions of LYCD were detected by mass spectrum (MS). In addition, LYCD of cells after UV or H2O2 are reported to be UV or H2O2 protective. We also looked into the effects of LYCD after plasma treatment by applying it to various types of cells subjected to plasma. Then Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) viabilities were measured by colony counting method, while Saccharomyces cerevisiae (S. cerevisiae), human breast cancer (MCF-7) and human embryonic skin fibroblasts (CCC-ESF-1) viabilities were assessed by XTT assay. The results indicated that the activities of SOD, CAT and the reduced GSH amount of LYCD increase linearly with plasma treatment time. More interestingly, those three important antioxidative substances extracted from yeast cell can act in accordance with each other. Furthermore, we observed that the LYCD induced by plasma can in turn effectively protect various types of cells from plasma damage. Detailed results will be discussed at the conference.
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