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过氧化氢对神经肽受体 PAC1-R 启动子活性的兴奋效应。

Hormesis effect of hydrogen peroxide on the promoter activity of neuropeptide receptor PAC1-R.

机构信息

Institute of Biomedicine, School of Life Science and Technology, Jinan University, Guangzhou, China.

National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou, China.

出版信息

J Food Biochem. 2019 Jul;43(7):e12877. doi: 10.1111/jfbc.12877. Epub 2019 Apr 26.

Abstract

Pituitary adenylate cyclase-activating polypeptide (PACAP) receptor 1 (PAC1-R) is the neuropeptide PACAP-preferring receptor-mediating neuroprotective activity. In order to clarify the biological mechanism of its expression, we cloned the 2,526 bp promoter fragment from -2,500 to +26 of the transcription initiation site of human ADCYAP1R1 gene and constructed the novel promotor reporter system named pYr-PromDetect-PAC1p. It was found in SH-SY5Y cells low concentration (<10 nM) of hydrogen peroxide (H O ) significantly promoted the activity of PAC1-R promoter in dose-dependent way, which was significantly inhibited by the transcription factor specificity protein 1 (SP1) inhibitor mithramycin A and was further confirmed in the deletion mutation of the predicted SP1 binding sites. Moreover, higher concentration of H O (>10 nM) inhibited the activity of PAC1-R in dose-dependent way. The hormesis effect of H O on PAC1-R promoter would help to further clarify the physiological effect of low-dose reactive oxygen on nervous system. PRACTICAL APPLICATIONS: PAC1-R mediates well-known neuroprotective, neurotrophic, and neurogenesis effects, which is an important drug target for neurodegenerative diseases. The hormesis effects of oxidative stress on PAC1-R expression not only help to explain the hormesis effects of oxidative stress on nerve system, but also offer a novel strategy to increase the expression of PAC1-R for the nerve protection or nerve generation. For example, taking advantage of low degree of oxidative stress to increases the expression of PAC1-R might help prevent subsequent surgical serious injury on the nervous system. The activation of PAC1-R promoter by low concentration of H O would help to further clarify the physiological effect of low-dose reactive oxygen on nervous system.

摘要

垂体腺苷酸环化酶激活肽(PACAP)受体 1(PAC1-R)是神经肽 PACAP 优先受体,介导神经保护活性。为了阐明其表达的生物学机制,我们从转录起始点-2500 到+26 克隆了人类 ADCYAP1R1 基因的 2526bp 启动子片段,并构建了新的启动子报告系统,命名为 pYr-PromDetect-PAC1p。研究发现,在 SH-SY5Y 细胞中,低浓度(<10 nM)的过氧化氢(H2O2)显著地以剂量依赖的方式促进 PAC1-R 启动子的活性,这种作用可被转录因子特异性蛋白 1(SP1)抑制剂米托蒽醌 A 显著抑制,并在预测的 SP1 结合位点缺失突变中得到进一步证实。此外,较高浓度的 H2O2(>10 nM)也以剂量依赖的方式抑制 PAC1-R 的活性。H2O2 对 PAC1-R 启动子的这种兴奋效应有助于进一步阐明低剂量活性氧对神经系统的生理作用。实际应用:PAC1-R 介导着众所周知的神经保护、神经营养和神经发生作用,这是神经退行性疾病的一个重要药物靶点。氧化应激对 PAC1-R 表达的兴奋效应不仅有助于解释氧化应激对神经系统的兴奋效应,而且为增加 PAC1-R 的表达以保护神经或促进神经发生提供了一种新策略。例如,利用低程度的氧化应激来增加 PAC1-R 的表达可能有助于预防随后对神经系统的严重手术损伤。H2O2 低浓度对 PAC1-R 启动子的激活有助于进一步阐明低剂量活性氧对神经系统的生理作用。

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