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Knockout of Ku86 accelerates cellular senescence induced by high NaCl

机译:Ku86的敲除加速了高NaCl诱导的细胞衰老

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摘要

NaCl induces DNA breaks, thus leading to cellular senescence. Here we showed that Ku86 deficiency accelerated the high NaCl-induced cellular senescence. We find that 1) high NaCl induces rapid cellular senescence in Ku86 deficient (xrs5) cells, 2) Ku86 deficiency shortens lifespan of C. elegans in high NaCl, and 3) cellular senescence is greatly accelerated in renal inner medullas of Ku86-/- mice. Further, although water balance is known to be compromised in old mice, this occurs at much earlier age in Ku86-/- mice. When subjected to mild water restriction, 3 month old Ku86-/-, but not Ku86+/+, mice rapidly become dehydrated as evidenced by decrease in body weight, increased production of antidiuretic hormone, increased urine osmolality and decreased urine volume. The deficiency in water balance does not occur in Ku86+/+mice until they are much older (14 months). We conclude that Ku86 deficiency accelerates high NaCl-induced cellular senescence, particularly in the renal medulla where NaCl normally is high.
机译:NaCl诱导DNA断裂,从而导致细胞衰老。在这里,我们显示Ku86缺乏促进了高NaCl诱导的细胞衰老。我们发现1)高NaCl在Ku86缺乏(xrs5)细胞中诱导快速细胞衰老,2)Ku86缺乏在高NaCl中缩短秀丽隐杆线虫的寿命,并且3)在Ku86的肾内髓质中细胞衰老大大加速。 -/-小鼠。此外,虽然已知水平衡在老年小鼠中受到损害,但这在Ku86 -/-小鼠中的年龄要早得多。当受到适度的水分限制(3个月大的Ku86 -/-)而不是Ku86 + / + 时,小鼠迅速脱水,表现为体重减轻,产量增加抗利尿激素,增加尿液渗透压和减少尿量。在Ku86 + / + 小鼠中不会出现水平衡不足的现象,直到它们大得多(14个月)为止。我们得出的结论是,Ku86缺乏会加速NaCl诱导的细胞衰老,特别是在NaCl通常较高的肾髓质中。

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