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首页> 外文期刊>Physiology International: Acta Physiologica Hungarica >Cocaine-and amphetamine-regulated transcript promoter regulated by nicotine in nerve growth factor-treated PC12 cells
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Cocaine-and amphetamine-regulated transcript promoter regulated by nicotine in nerve growth factor-treated PC12 cells

机译:可卡因和安非他明调节的转录子受神经生长因子处理的PC12细胞中的尼古丁调节

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摘要

Nicotine and cocaine- and amphetamine-regulated transcripts (CART) have several overlapping functions, such as the regulation of reward, feeding behavior, stress response, and anxiety. Previous studies showed that nicotine regulates CART expression in various brain regions. However, the molecular mechanisms underlying this regulation are not known. This study investigated the regulatory effect of nicotine on promoter activity of the CART gene in PC12 cells, which were differentiated into a neuronal phenotype by nerve growth factor (NGF) treatment. Two vectors containing reporter genes (Gaussia luciferase or mCherry) and the 1,140-bp upstream of the transcriptional start site of the mouse CART gene are used to analyze the CART promoter activity. Transient transfection of PC12 cells with either vector displayed strong promoter activity in both undifferentiated and differentiated PC12 cells. CART promoter activity in the PC12 cell line is increased by forskolin or NGF treatment. In differentiated PC12 cells, exposure to 50 nM nicotine for 6 h increased CART promoter activity. However, treatment with higher nicotine doses for 6 h and treatment with all nicotine doses for 24 h showed no effect. A nicotine concentration of 50 nM is comparable to brain nicotine levels experienced by chronic smokers over long periods of time. Taken together, these data indicate that nicotine may exert some of its actions through the regulation of CART transcription in the brain.
机译:尼古丁和可卡因和安非胺调节的转录物(推车)具有几种重叠功能,例如奖励的调节,喂养行为,压力反应和焦虑。以前的研究表明,尼古丁调节各种脑区中的推车表达。然而,该调节的潜在的分子机制尚不清楚。本研究调查了尼古丁对PC12细胞中推车基因启动子活性的调节作用,其通过神经生长因子(NGF)处理分为神经元表型。含有报告基因(高斯荧光素酶或MCHERRY)的两种载体和小鼠购物车基因的转录起始位点上游的1,140bp用于分析推车启动子活性。在未分化的和分化的PC12细胞中,在任何一种载体中显示PC12细胞的瞬时转染。通过Forskolin或NGF治疗增加了PC12细胞系中PC12细胞系的推动者活性。在分化的PC12细胞中,暴露于50nm尼古丁6小时的推车启动子活性。然而,用较高的尼古丁剂量进行6小时的处理和用所有尼古丁剂量治疗24小时显示没有效果。尼古丁浓度为50nm,与长时间慢性吸烟者经历的脑尼古丁水平相当。总之,这些数据表明尼古丁可以通过脑中的推车转录来发挥其一些动作。

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