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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:通过结合微电子学和细胞生物学的基于阻抗的信号处理技术,对人颗粒细胞进行实时和无标记监测的细胞毒性和促有丝分裂测定

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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:集成微电子学和细胞生物学的最新开发的技术(xCelligence)可以通过不使用任何标记剂的情况下测量孔中细胞群体的电阻抗,从而对细胞增殖,生存力和细胞毒性进行实时,不间断和定量的分析。在这项研究中,我们调查了该系统是否适合用于分析与常规评估细胞活力,DNA损伤,细胞凋亡和凋亡的常规方法相比,具有不同毒性谱的促细胞分裂剂(FSH)和细胞毒性(化学疗法)剂对人颗粒细胞的影响。类固醇生成。该系统生成细胞的实时生长曲线,并确定它们的倍增时间,平均细胞指数并在暴露于细胞毒性和促有丝分裂的刺激后生成剂量反应曲线。它准确地预测了药物的性腺毒性,并将毒性较低的药物(5-FU和紫杉醇)与毒性较高的药物(顺铂和环磷酰胺)区分开来。该平台可以用作生殖毒理学中特定终点检测的有用工具。 (C)2015 Elsevier Inc.保留所有权利。

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