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首页> 外文期刊>International Journal of Molecular Sciences >Nanosecond-Pulsed DBD Plasma-Generated Reactive Oxygen Species Trigger Immunogenic Cell Death in A549 Lung Carcinoma Cells through Intracellular Oxidative Stress
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Nanosecond-Pulsed DBD Plasma-Generated Reactive Oxygen Species Trigger Immunogenic Cell Death in A549 Lung Carcinoma Cells through Intracellular Oxidative Stress

机译:纳秒脉冲DBD血浆产生的活性氧物种通过细胞内氧化应激触发A549肺癌细胞的免疫原性细胞死亡。

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A novel application for non-thermal plasma is the induction of immunogenic cancer cell death for cancer immunotherapy. Cells undergoing immunogenic death emit danger signals which facilitate anti-tumor immune responses. Although pathways leading to immunogenic cell death are not fully understood; oxidative stress is considered to be part of the underlying mechanism. Here; we studied the interaction between dielectric barrier discharge plasma and cancer cells for oxidative stress-mediated immunogenic cell death. We assessed changes to the intracellular oxidative environment after plasma treatment and correlated it to emission of two danger signals: surface-exposed calreticulin and secreted adenosine triphosphate. Plasma-generated reactive oxygen and charged species were recognized as the major effectors of immunogenic cell death. Chemical attenuators of intracellular reactive oxygen species successfully abrogated oxidative stress following plasma treatment and modulated the emission of surface-exposed calreticulin. Secreted danger signals from cells undergoing immunogenic death enhanced the anti-tumor activity of macrophages. This study demonstrated that plasma triggers immunogenic cell death through oxidative stress pathways and highlights its potential development for cancer immunotherapy.
机译:非热血浆的一种新应用是诱导用于癌症免疫疗法的免疫原性癌细胞死亡。经历免疫原性死亡的细胞会发出危险信号,从而促进抗肿瘤免疫反应。尽管导致免疫原性细胞死亡的途径尚不完全清楚。氧化应激被认为是潜在机制的一部分。这里;我们研究了介电屏障放电血浆与癌细胞之间的相互作用,用于氧化应激介导的免疫原性细胞死亡。我们评估了血浆处理后细胞内氧化环境的变化,并将其与两个危险信号的发射相关:表面暴露的钙网蛋白和分泌的三磷酸腺苷。血浆产生的活性氧和带电物质被认为是免疫原性细胞死亡的主要效应器。细胞内活性氧的化学衰减剂在等离子体处理后成功消除了氧化应激并调节了表面暴露的钙网蛋白的发射。来自经历免疫原性死亡的细胞的分泌的危险信号增强了巨噬细胞的抗肿瘤活性。这项研究表明血浆通过氧化应激途径触发免疫原性细胞死亡,并突出了其在癌症免疫疗法中的潜在发展。

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