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
Charité, Campus Benjamin Franklin, Institute of Physiology, Arnimallee 22, 14195 Berlin, Germany.
FEBS Lett. 2007 Feb 20;581(4):673-80. doi: 10.1016/j.febslet.2007.01.028. Epub 2007 Jan 22.
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.
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。