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一氧化氮刺激胰腺β细胞中的胰岛素基因转录。

Nitric oxide stimulates insulin gene transcription in pancreatic beta-cells.

作者信息

Campbell S C, Richardson H, Ferris W F, Butler C S, Macfarlane W M

机构信息

Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Biochem Biophys Res Commun. 2007 Feb 23;353(4):1011-6. doi: 10.1016/j.bbrc.2006.12.127. Epub 2006 Dec 26.

Abstract

Recent studies have identified a positive role for nitric oxide (NO) in the regulation of pancreatic beta-cell function. The aim of this study was to determine the effects of short-term exposure to NO on beta-cell gene expression and the activity of the transcription factor PDX-1. NO stimulated the activity of the insulin gene promoter in Min6 beta-cells and endogenous insulin mRNA levels in both Min6 and isolated islets of Langerhans. Addition of wortmannin prior to NO stimulation blocked the observed increases in insulin gene promoter activity. Although NO addition stimulated the phosphorylation of p38, inhibition by SB203580 did not block the effect of NO on the insulin gene promoter. NO addition also stimulated both the nuclear accumulation and the DNA binding activity of PDX-1. This study has shown that over 24h, NO stimulates insulin gene expression, PI-3-kinase activity and the activity of the critical beta-cell transcription factor PDX-1.

摘要

最近的研究已经确定一氧化氮(NO)在胰腺β细胞功能调节中发挥着积极作用。本研究的目的是确定短期暴露于NO对β细胞基因表达和转录因子PDX-1活性的影响。NO刺激了Min6β细胞中胰岛素基因启动子的活性以及Min6和分离的胰岛中内源性胰岛素mRNA水平。在NO刺激之前添加渥曼青霉素可阻断观察到的胰岛素基因启动子活性的增加。尽管添加NO刺激了p38的磷酸化,但SB203580的抑制作用并未阻断NO对胰岛素基因启动子的影响。添加NO还刺激了PDX-1的核积累和DNA结合活性。这项研究表明,在24小时以上的时间里,NO刺激胰岛素基因表达、PI-3激酶活性以及关键的β细胞转录因子PDX-1的活性。

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