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通过监测细胞培养中的过氧化氢来评估细胞死亡研究。

Assessment of cell death studies by monitoring hydrogen peroxide in cell culture.

作者信息

Hirsch Irina, Prell Erik, Weiwad Matthias

机构信息

Max Planck Research Unit for Enzymology of Protein Folding, Weinbergweg 22, 06120 Halle, Germany.

Max Planck Research Unit for Enzymology of Protein Folding, Weinbergweg 22, 06120 Halle, Germany.

出版信息

Anal Biochem. 2014 Jul 1;456:22-4. doi: 10.1016/j.ab.2014.04.009. Epub 2014 Apr 18.

Abstract

Hydrogen peroxide (H2O2) has been widely used to study the oxidative stress response. However, H2O2 is unstable and easily decomposes into H2O and O2. Consequently, a wide range of exposure times and treatment concentrations has been described in the literature. In the present study, we established a ferrous oxidation-xylenol orange (FOX) assay, which was originally described for food and body liquids, as a method for the precise quantification of H2O2 concentrations in cell culture media. We observed that the presence of FCS and high cell densities significantly accelerate the decomposition of H2O2, therefore acting as a protection against cell death by accidental necrosis.

摘要

过氧化氢(H2O2)已被广泛用于研究氧化应激反应。然而,H2O2不稳定,容易分解为H2O和O2。因此,文献中描述了广泛的暴露时间和处理浓度。在本研究中,我们建立了一种亚铁氧化-二甲酚橙(FOX)测定法,该方法最初用于食品和体液,作为精确量化细胞培养基中H2O2浓度的方法。我们观察到,胎牛血清(FCS)的存在和高细胞密度会显著加速H2O2的分解,从而起到防止意外坏死导致细胞死亡的作用。

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