分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Myricetin protects natural killer cells from arsenite induced DNA damage by attenuating oxidative stress and retaining poly(ADP-Ribose) polymerase 1 activity

Huijuan Ma, Xiaodong Song, Ping Huang, Weiwei Zhang, Xinyue Ling, Xiaoning Yang, Wenwei Wu, Huan Xu, Wei Wang

Journal:MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS

IF:2.87

DOI:10.1016/j.mrgentox.2021.503337

PMID:33865543

Published:2021-02-19

research field:

Abstract

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.

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