首页> 外文期刊>The international journal of biochemistry and cell biology >Resveratrol increases anti-aging Klotho gene expression via the activating transcription factor 3/c-Jun complex-mediated signaling pathway
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Resveratrol increases anti-aging Klotho gene expression via the activating transcription factor 3/c-Jun complex-mediated signaling pathway

机译:白藜芦醇通过激活转录因子3 / c-Jun复合物介导的信号通路增加抗衰老Klotho基因表达

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摘要

The Klotho gene functions as an aging suppressor gene. Evidence from animal models suggests that induction of Klotho expression may be a potential treatment for age-associated diseases. However, the molecular mechanism involved in regulating renal Klotho gene expression remains unclear. In this study, we determined that resveratrol, a natural polyphenol, induced renal Klotho expression both in vivo and in vitro. In the mouse kidney, resveratrol administration markedly increased both Klotho mRNA and protein expression. In resveratrol-treated NRK-52E cells, increased Klotho expression was accompanied by the upregulation and nuclear translocation of activating transcription factor 3 (ATF3) and c-Jun. ATF3 or c-Jun overexpression enhanced the transcriptional activation of Klotho. Conversely, resveratrol-induced Klotho expression was attenuated in the presence of dominant-negative ATF3 or c-Jun. Coimmunoprecipitation and a chromatin immunoprecipitation assay revealed that ATF3 physically interacted with c-Jun and that the ATF3/c-Jun complex directly bound to the Klotho promoter through ATF3- and AP-1 -binding elements. c-Jun cotransfection augmented the effects of ATF3 on Klotho transcription in vitro. Although Sirtuin 1 mRNA expression was induced by resveratrol and involved in regulating Klotho mRNA expression, it was not the primary cause for the aforementioned ATF3/c-Jun pathway. In summary, resveratrol enhances the renal expression of the anti-aging Klotho gene, and the transcriptional factors ATF3 and c-Jun functionally interact and coordinately regulate the resveratrol-mediated transcriptional activation of Klotho.
机译:Klotho基因起衰老抑制基因的作用。动物模型的证据表明,诱导Klotho表达可能是与年龄有关的疾病的潜在治疗方法。但是,尚不清楚调控肾脏Klotho基因表达的分子机制。在这项研究中,我们确定白藜芦醇(一种天然多酚)在体内和体外均可诱导肾脏Klotho表达。在小鼠肾脏中,白藜芦醇给药可显着增加Klotho mRNA和蛋白质表达。在白藜芦醇处理的NRK-52E细胞中,Klotho表达的增加伴随着活化转录因子3(ATF3)和c-Jun的上调和核转位。 ATF3或c-Jun过表达增强了Klotho的转录激活。相反,在显性阴性ATF3或c-Jun的存在下,白藜芦醇诱导的Klotho表达减弱。免疫共沉淀和染色质免疫沉淀测定表明,ATF3与c-Jun物理相互作用,并且ATF3 / c-Jun复合物通过ATF3-和AP-1结合元件直接与Klotho启动子结合。 c-Jun共转染增强了ATF3对体外Klotho转录的影响。尽管白藜芦醇诱导Sirtuin 1 mRNA表达并参与调节Klotho mRNA表达,但它不是上述ATF3 / c-Jun途径的主要原因。总之,白藜芦醇增强了抗衰老Klotho基因的肾脏表达,转录因子ATF3和c-Jun在功能上相互作用并协调调节白藜芦醇介导的Klotho转录激活。

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