Kobashigawa Shinko, Kashino Genro, Mori Hiromu, Watanabe Masami
Department of Radiology, School of Medicine, Oita University, Oita, Japan.
Advanced Molecular Imaging Center, School of Medicine, Oita University, Oita, Japan.
Mech Ageing Dev. 2015 Mar;146-148:65-71. doi: 10.1016/j.mad.2015.05.002. Epub 2015 May 6.
Ionizing radiation-induced cellular senescence is thought to be caused by nuclear DNA damage that cannot be repaired. However, here we found that radiation induces delayed increase of intracellular oxidative stress after irradiation. We investigated whether the relief of delayed oxidative stress by ascorbic acid would suppress the radiation-induced cellular senescence in Syrian golden hamster embryo (SHE) cells. We observed that the level of oxidative stress was drastically increased soon after irradiation, then declined to the level in non-irradiated cells, and increased again with a peak on day 3 after irradiation. We found that the inductions of cellular senescence after X-irradiation were reduced along with suppression of the delayed induction of oxidative stress by treatment with ascorbic acid, but not when oxidative stress occurred immediately after irradiation. Moreover, treatment of ascorbic acid inhibited p53 accumulation at 3 days after irradiation. Our data suggested a delayed increase of intracellular oxidative stress levels plays an important role in the process of radiation-induced cellular senescence by p53 accumulation.
电离辐射诱导的细胞衰老被认为是由无法修复的核DNA损伤引起的。然而,我们在此发现,辐射会在照射后诱导细胞内氧化应激的延迟增加。我们研究了抗坏血酸缓解延迟氧化应激是否会抑制叙利亚金仓鼠胚胎(SHE)细胞中辐射诱导的细胞衰老。我们观察到,照射后氧化应激水平很快急剧升高,然后下降到未照射细胞的水平,并在照射后第3天再次升高并达到峰值。我们发现,X射线照射后细胞衰老的诱导随着抗坏血酸处理对氧化应激延迟诱导的抑制而减少,但在照射后立即出现氧化应激时则不会减少。此外,抗坏血酸处理在照射后3天抑制了p53的积累。我们的数据表明,细胞内氧化应激水平的延迟增加通过p53积累在辐射诱导的细胞衰老过程中起重要作用。