Igarashi Kintaro, Shoji Yoshimi, Sekine-Suzuki Emiko, Ueno Megumi, Matsumoto Ken-Ichiro, Nakanishi Ikuo, Fukui Koji
Molecular Cell Biology Laboratory, Department of Bioscience and Engineering, College of Systems Engineering and Science, Shibaura Institute of Technology, Fukasaku 307, Minuma-ku, Saitama 337-8570, Japan.
Quantitative RedOx Sensing Group, Department of Radiation Regulatory Science Research, National Institute of Radiological Sciences, Quantum Life and Medical Science Directorate, National Institutes for Quantum Science and Technology, 4-9-1 Anagawa, Inage-ku, Chiba-shi 263-8555, Japan.
Cancers (Basel). 2022 Jul 27;14(15):3642. doi: 10.3390/cancers14153642.
The impact of the site of the Fenton reaction, i.e., hydroxyl radical (OH) generation, on cytotoxicity was investigated by estimating cell lethality in rat thymocytes. Cells were incubated with ferrous sulfate (FeSO) and hydrogen peroxide (HO), or pre-incubated with FeSO and then HO was added after medium was replaced to remove iron ions or after the medium was not replaced. Cell lethality in rat thymocytes was estimated by measuring cell sizes using flow cytometry. High extracellular concentrations of FeSO exerted protective effects against HO-induced cell death instead of enhancing cell lethality. The pre-incubation of cells with FeSO enhanced cell lethality induced by HO, whereas a pre-incubation with a high concentration of FeSO exerted protective effects. FeSO distributed extracellularly or on the surface of cells neutralized HO outside cells. Cytotoxicity was only enhanced when the Fenton reaction, i.e., the generation of OH, occurred inside cells. An assessment of plasmid DNA breakage showed that OH induced by the Fenton reaction system did not break DNA. Therefore, the main target of intracellularly generated OH does not appear to be DNA.
通过评估大鼠胸腺细胞的细胞致死率,研究了芬顿反应位点(即羟基自由基(·OH)的产生)对细胞毒性的影响。将细胞与硫酸亚铁(FeSO₄)和过氧化氢(H₂O₂)一起孵育,或者先与FeSO₄预孵育,然后在更换培养基以去除铁离子后或不更换培养基的情况下添加H₂O₂。通过使用流式细胞术测量细胞大小来评估大鼠胸腺细胞的细胞致死率。高细胞外浓度的FeSO₄对H₂O₂诱导的细胞死亡具有保护作用,而不是增强细胞致死率。细胞与FeSO₄预孵育会增强H₂O₂诱导的细胞致死率,而高浓度FeSO₄预孵育则具有保护作用。细胞外分布或细胞表面的FeSO₄中和了细胞外的H₂O₂。只有当芬顿反应(即·OH的产生)在细胞内发生时,细胞毒性才会增强。对质粒DNA断裂的评估表明,芬顿反应系统诱导的·OH不会断裂DNA。因此,细胞内产生的·OH的主要靶点似乎不是DNA。