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Myricetin protects natural killer cells from arsenite induced DNA damage by attenuating oxidative stress and retaining poly(ADP-Ribose) polymerase 1 activity
Mutation Research/Genetic Toxicology and Environmental Mutagenesis ( IF 2.3 ) Pub Date : 2021-02-19 , DOI: 10.1016/j.mrgentox.2021.503337
Huijuan Ma 1 , Xiaodong Song 2 , Ping Huang 1 , Weiwei Zhang 1 , Xinyue Ling 1 , Xiaoning Yang 1 , Wenwei Wu 1 , Huan Xu 1 , Wei Wang 3
Affiliation  

Environmental exposure to arsenite (As+3) is known to induce immunotoxicity. Natural killer (NK) cells are innate lymphoid cells act as professional killers of tumor cells. Our previous report indicated that 500 ppb As+3 drinking water exposure induced significant DNA damage in the NK cells of C57BL/6 mice. Myricetin is a plant-derived flavonoid known as a strong antioxidant. In this study, daily administration of myricetin at 20 mg/kg was found to alleviate the cell population decrease and DNA damage in the NK cells of BALB/c mice exposed to 500 and 1000 ppb As+3 via drinking water. Oxidative stress and poly(ADP-ribose) polymerase 1 (PARP-1) inhibition were induced by As+3 at 1 and 2 μM in isolated mouse NK cells in vitro, which were attenuated by 20 μM myricetin. The mitigatory effect of myricetin on the PARP-1 inhibition in NK cells treated with As+3 was also found to be the result of its prevention of the zinc loss induced by As+3 on PARP-1. Collectively, these results demonstrated, for the first time, that myricetin could protect NK cells from As+3 induced DNA through attenuating oxidative stress and retaining PARP-1 activity, indicating that myricetin may be utilized for the prevention of the immunotoxicity induced by As+3 in NK cells.



中文翻译:

杨梅素通过减弱氧化应激和保留聚(ADP-核糖)聚合酶 1 活性来保护自然杀伤细胞免受亚砷酸盐诱导的 DNA 损伤

已知环境暴露于亚砷酸盐 (As +3 ) 会诱发免疫毒性。自然杀伤 (NK) 细胞是先天淋巴细胞,充当肿瘤细胞的专业杀手。我们之前的报告表明,500 ppb As +3饮用水暴露在 C57BL/6 小鼠的 NK 细胞中诱导了显着的 DNA 损伤。杨梅素是一种植物来源的黄酮类化合物,被称为强抗氧化剂。在这项研究中,发现每天以 20 mg/kg 的剂量施用杨梅素可以缓解通过饮用水暴露于 500 和 1000 ppb As +3的 BALB/c 小鼠 NK 细胞的细胞数量减少和 DNA 损伤。在分离的小鼠 NK 细胞中,1 μM 和 2 μM的 As +3诱导氧化应激和聚(ADP-核糖)聚合酶 1 (PARP-1) 抑制体外,其被 20 μM 杨梅素减弱。杨梅素对用 As +3处理的 NK 细胞中 PARP-1 抑制的缓解作用也被发现是其预防由 As +3对 PARP-1诱导的锌损失的结果。总的来说,这些结果首次表明,杨梅素可以通过减弱氧化应激和保留 PARP-1 活性来保护 NK 细胞免受 As +3诱导的 DNA 的影响,表明杨梅素可用于预防 As +诱导的免疫毒性。3在 NK 细胞中。

更新日期:2021-02-26
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