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The effects of perfluorooctane sulfonate(PFOS) on proliferation of mouse leydig cells in vitro

机译:全氟辛烷磺酸盐(PFOS)对体外小鼠Leydig细胞增殖的影响

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To evaluate the male reproductive toxicity of PFOS on mammal animals at cellular level, mouse leydig cells were isolated from healthy mouse testis tissue and cultured in vitro. Adherent cells were treated with a serial concentration of PFOS for 4 more days of culture. Proliferation and DNA damage of the cells were analyzed by CCK assay and SCGE assay respectively. Forty-eight hours of treating with PFOS ≥ 25μg/mL all inhibited the proliferation of the cells(p<0.05). PFOS seemed not to change the time for the cells to reach platform phase. DNA damage was also observed in the groups treated with PFOS dependent on dose and exposure time. The highest DNA damage level was averagely 17 cells per well in 96-well plates, which occurred to 62.5μg/mL group at 72h.
机译:为了评估细胞水平的哺乳动物动物对哺乳动物动物的雄性生殖毒性,小鼠leydig细胞与健康小鼠睾丸组织分离并在体外培养。将粘附细胞用串联浓度的PFOS治疗4天培养。通过CCK测定和SCGE测定分析细胞的增殖和DNA损伤。用PFOS≥25μg/ ml的四十八小时均抑制细胞的增殖(P <0.05)。 PFOS似乎不会改变细胞到达平台阶段的时间。在用PFOS依赖于剂量和暴露时间处理的基团中也观察到DNA损伤。在96孔板中,最高DNA损伤水平平均为17个细胞,在96孔板中,在72h时发生62.5μg/ ml。

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