首页> 外文期刊>Cell Stress and Chaperones >The Nrf2–Keap1 cellular defense pathway and heat shock protein 70 (Hsp70) response. Role in protection against oxidative stress in early neonatal unilateral ureteral obstruction (UUO)
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The Nrf2–Keap1 cellular defense pathway and heat shock protein 70 (Hsp70) response. Role in protection against oxidative stress in early neonatal unilateral ureteral obstruction (UUO)

机译:Nrf2-Keap1细胞防御途径和热休克蛋白70(Hsp70)反应。在早期新生儿单侧输尿管梗阻(UUO)中抗氧化应激的保护作用

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Perturbation of renal tubular antioxidants and overproduction of reactive oxygen species may amplify the proinflammatory state of renal obstruction, culminating in oxidative stress and tubular loss. Here, we analyzed the heat shock protein 70 (Hsp70) response and the function and signal transduction of NF-E2-related protein 2 (Nrf2) transcription factor on oxidative stress modulation in obstruction. Rats were subjected to unilateral ureteral obstruction or sham operation and kidneys harvested at 5, 7, 10, and 14 days after obstruction. Hsp70 expression and Nrf2 activity and its downstream target gene products were assessed. After 10 and 14 days of obstruction, enhanced lipid peroxidation through higher thiobarbituric acid reactive substances levels and increased oxidative stress resulted in reduced total antioxidant activity and enhanced nicotinamide adenine dinucleotide phosphate reduced (NADPH) oxidase activity were demonstrated. This was accompanied by decreased inducible Hsp70 expression and a progressive reduction of nuclear Nrf2 and its target gene products glutathione S-transferase A2 (GSTA2) and NADPH/quinone oxidoreductase 1 (NQO1), whereas the Nrf2 repressor Kelch-like ECH-associated protein-1 (Keap1) was upregulated. By contrast, on early obstruction for 7 days, lack of increased oxidative markers associated with higher inducible Hsp70 protein levels and a rapid nuclear accumulation of Nrf2, Keap1 downregulation, and mRNA induction of the identified Nrf2-dependent genes, NQO1 and GSTA2, were shown. For these results, we suggest that the magnitude of cytoprotection in early obstruction depends on the combined contribution of induced activation of Nrf2 upregulating its downstream gene products and Hsp70 response. Impaired ability to mount the biological response to the prevailing oxidative stress leading to renal injury was shown in prolonged obstruction.
机译:肾小管抗氧化剂的摄动和活性氧的过量产生可能会放大肾梗阻的促炎状态,最终导致氧化应激和肾小管丢失。在这里,我们分析了热休克蛋白70(Hsp70)的响应以及NF-E2相关蛋白2(Nrf2)转录因子对阻塞性氧化应激调节的功能和信号转导。对大鼠进行单侧输尿管阻塞或假手术,在阻塞后第5、7、10和14天收获肾脏。 Hsp70表达和Nrf2活性及其下游目标基因产物进行了评估。梗阻10天和14天后,通过更高的硫代巴比妥酸反应性物质水平增强的脂质过氧化作用和增加的氧化应激导致总抗氧化剂活性降低,烟酰胺腺嘌呤二核苷酸磷酸还原(NADPH)氧化酶活性增强。这伴随着诱导型Hsp70表达的降低和核Nrf2及其靶基因产物谷胱甘肽S-转移酶A2(GSTA2)和NADPH /醌氧化还原酶1(NQO1)的逐渐减少,而Nrf2阻遏物与Kelch样ECH相关的蛋白1(Keap1)被上调。相比之下,在早期阻塞7天时,显示出缺乏与较高的可诱导Hsp70蛋白水平和Nrf2的快速核积累,Keap1下调以及已鉴定的Nrf2依赖性基因NQO1和GSTA2的mRNA诱导相关的氧化标记。 。对于这些结果,我们建议早期梗阻中的细胞保护程度取决于诱导激活的Nrf2上调其下游基因产物和Hsp70反应的组合作用。在长时间的梗阻中显示出对主要的氧化应激导致肾脏损伤的生物反应能力减弱。

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