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Cytotoxicity and mitogenicity assays with real-time and label-free monitoring of human granulosa cells with an impedance-based signal processing technology intergrating micro-electronics and cell biology

机译:具有基于阻抗的信号处理技术整形微电子和细胞生物学的人颗粒细胞对人颗粒细胞的实时和无丝发液性测定。

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摘要

A recently developed technology (xCelligence) integrating micro-electronics and cell biology allows real-time, uninterrupted and quantitative analysis of cell proliferation, viability and cytotoxicity by measuring the electrical impedance of the cell population in the wells without using any labeling agent. In this study we investigated if this system is a suitable model to analyze the effects of mitogenic (FSH) and cytotoxic (chemotherapy) agents with different toxicity profiles on human granulosa cells in comparison to conventional methods of assessing cell viability, DNA damage, apoptosis and steroidogenesis. The system generated the real-time growth curves of the cells, and determined their doubling times, mean cell indices and generated dose-response curves after exposure to cytotoxic and mitogenic stimuli. It accurately predicted the gonadotoxicity of the drugs and distinguished less toxic agents (5-FU and paclitaxel) from more toxic ones (cisplatin and cyclophosphamide). This platform can be a useful tool for specific end-point assays in reproductive toxicology. (C) 2015 Elsevier Inc. All rights reserved.
机译:最近开发的技术(Xcelligence)整合微电子和细胞生物学通过测量孔中细胞群的电阻抗而不使用任何标记剂,可以实时,不间断和定量分析细胞增殖,活力和细胞毒性。在该研究中,我们研究了该系统是否是分析丝肠(FSH)和细胞毒性(化疗)药物在人颗粒细胞上用不同毒性谱的影响的合适模型,与评估细胞活力,DNA损伤,细胞凋亡和细胞凋亡的常规方法相比甾体系。该系统产生了细胞的实时生长曲线,并确定了它们的倍数,平均细胞索引和暴露于细胞毒性和促毒性刺激后产生的剂量 - 反应曲线。它准确地预测了药物的促毒性,以及从更多毒毒性的药物(5-FU和PACLITAXEL)的毒性毒性(顺铂和环磷酰胺)。该平台可以是生殖毒理学中特定终点测定的有用工具。 (c)2015 Elsevier Inc.保留所有权利。

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