Suppr超能文献

剪切应力对Foxo-1及血管生成素-2/Tie2系统的调控

Regulation of Foxo-1 and the angiopoietin-2/Tie2 system by shear stress.

作者信息

Chlench Sven, Mecha Disassa Nigussie, Hohberg Margret, Hoffmann Christian, Pohlkamp Theresa, Beyer Gabriele, Bongrazio Mauro, Da Silva-Azevedo Luis, Baum Oliver, Pries Axel Radlach, Zakrzewicz Andreas

机构信息

Charité, Campus Benjamin Franklin, Institute of Physiology, Arnimallee 22, 14195 Berlin, Germany.

出版信息

FEBS Lett. 2007 Feb 20;581(4):673-80. doi: 10.1016/j.febslet.2007.01.028. Epub 2007 Jan 22.

Abstract

Transcription factor Foxo-1 can be inactivated via Akt-mediated phosphorylation. Since shear stress activates Akt, we determined whether Foxo-1 and the Foxo-1-dependent, angiogenesis-related Ang-2/Tie2-system are influenced by shear stress in endothelial cells. Expression of Foxo-1 and its target genes p27Kip1 and Ang-2 was decreased under shear stress (6dyn/cm(2), 24h), nuclear exclusion of Foxo-1 by phosphorylation increased. eNOS and Tie2 were upregulated. No effects on Ang-1 expression were detected. In conclusion, Foxo-1 and Ang-2/Tie2 are part of the molecular response to shear stress, which may regulate angiogenesis.

摘要

转录因子Foxo-1可通过Akt介导的磷酸化作用而失活。由于剪切应力可激活Akt,我们研究了内皮细胞中的剪切应力是否会影响Foxo-1以及与Foxo-1相关的、血管生成相关的Ang-2/Tie2系统。在剪切应力(6达因/平方厘米,24小时)作用下,Foxo-1及其靶基因p27Kip1和Ang-2的表达降低,Foxo-1因磷酸化而被核排除的情况增加。eNOS和Tie2上调。未检测到对Ang-1表达有影响。总之,Foxo-1和Ang-2/Tie2是对剪切应力分子反应的一部分,这可能调节血管生成。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验