首页> 外文期刊>Free radical research >Repression of apurinic/apyrimidinic endonuclease by p53-dependent apoptosis in hydronephrosis-induced rat kidney.
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Repression of apurinic/apyrimidinic endonuclease by p53-dependent apoptosis in hydronephrosis-induced rat kidney.

机译:p53依赖性细胞凋亡在肾积水诱导的大鼠肾脏中抑制嘌呤/嘧啶内切核酸酶。

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摘要

p53 plays a major role in apoptosis through activation of pro-apoptotic gene Bax. It also regulates apurinic/apyrimidinic endonuclease (APE) expression in the base excision repair pathway against oxidative DNA damages. This study investigated whether p53-dependent apoptosis is correlated with APE using an experimental rat model of hydronephrosis. Hydronephrosis was induced by partial ligation of the right ureter. Animals were sacrificed on scheduled time after unilateral ureteral obstruction and the expression of 8-OHdG, gamma-H2AX, apoptotic proteins and APE was determined. The accumulated p53 activated Bax and caspase-3 7 days after hydronephrosis induction and the resulting high levels of p53-dependent apoptotic proteins and gamma-H2AX tended to decrease APE. The intensities of 8-OHdG and caspase-3 immunolocalization significantly increased in obstructed kidneys than in sham-operated kidneys, although APE immunoreactivity increased after hydronephrosis induction. These results suggest that oxidative DNA damages in obstructed kidneys may trigger p53-dependent apoptosis through repression of APE.
机译:p53通过激活促凋亡基因Bax在凋亡中起主要作用。它还调节碱基切除修复途径中的嘌呤/嘧啶内切核酸酶(APE)表达,以抵抗氧化性DNA损伤。这项研究使用大鼠肾积水模型研究了p53依赖性细胞凋亡是否与APE相关。右输尿管部分结扎可引起肾积水。在单侧输尿管阻塞后的预定时间处死动物,并测定8-OHdG,γ-H2AX,凋亡蛋白和APE的表达。肾积水诱导7天后,积累的p53激活了Bax和caspase-3,因此,高水平的p53依赖性凋亡蛋白和γ-H2AX倾向于降低APE。尽管肾盂积水诱导后APE免疫反应性增加,但阻塞性肾脏的8-OHdG和caspase-3免疫定位的强度明显高于假手术肾脏。这些结果表明,阻塞性肾脏中的氧化DNA损伤可能通过抑制APE触发p53依赖性细胞凋亡。

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