PurA sensitizes cells to toxicity induced by oxidative stress

Hawra Albukhaytan, B. Torkzaban, I. Sariyer, S. Amini
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Abstract

Abstract Objectives PurA is an evolutionary conserved protein that is known to bind to single stranded DNA or RNA and regulate both transcription and translation. PurA has been implicated in many neurological and neurodevelopmental deficits, but its role in response to cellular stress has not yet been clarified. In this study, we have studied the cells’ stress response in the presence and absence of PurA expression. Methods Oxidative stress was induced in MEF cells obtained from PURA WT and K/O mice by paraquat treatments. The cellular response to stress was determined and compared by viability assays, immunocytochemistry and biochemical analyses. Results Interestingly, paraquat treated PurA expressing MEF cells showed higher sensitivity and less cellular viability than those with no PurA expression. Moreover, western blot analysis revealed increase in the expression of the apoptotic marker cleaved caspase 3 and autophagy marker LC3-II in PurA WT MEF cells compared to the PurA K/O MEF cells under oxidative stress induction. Conclusions Our observations indicate that PurA may play a key role in regulating cellular toxicity induced by oxidative stress and emphasize its importance for cell-fate determination under cytotoxic stress conditions.
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PurA使细胞对氧化应激引起的毒性敏感
摘要目的PurA是一种进化保守蛋白,已知与单链DNA或RNA结合并调节转录和翻译。PurA与许多神经和神经发育缺陷有关,但其在细胞应激反应中的作用尚未阐明。在这项研究中,我们研究了在存在和不存在PurA表达的情况下细胞的应激反应。方法用百草枯诱导PURA WT和K/O小鼠MEF细胞氧化应激。通过活力测定、免疫细胞化学和生化分析测定并比较细胞对应激的反应。结果有趣的是,百草枯处理的表达PurA的MEF细胞显示出比不表达PurA细胞更高的敏感性和更低的细胞活力。此外,蛋白质印迹分析显示,与氧化应激诱导下的PurA K/O MEF细胞相比,PurA WT MEF细胞中凋亡标记物裂解的胱天蛋白酶3和自噬标记物LC3-II的表达增加。结论我们的观察结果表明,PurA可能在调节氧化应激诱导的细胞毒性中发挥关键作用,并强调其在细胞毒性应激条件下对细胞命运测定的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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