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Expression of AQP1 in Vascular Endothelia Cells during Angiogenesis Is Associated with MRTF-A

机译:在血管生成期间AQP1在血管内皮细胞中的表达与MRTF-A有关

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Recent studies have demonstrated that the expression of aquaporin1 (AQP1) in endothelia cells played important roles in cell migration, and migration-associated cell function such as wound healing, and neutrophil motility. In the present study, we provided evidence that AQP1 expression in vascular endothelia cells (VECs) during angiogenesis was associated with MRTF-A. Morphology and immunofluorescence assay demonstrated that VECs from normal and angiogenesis tissues had similar appearance. Reverse Transcription-Polymerase Chain Reaction (RT-PCR), Immunoblot and Immunofluorescence analysis identified that AQP1 expression was significantly higher in angiogenesis VECs than in normal VECs. MRTF-A expression was also remarkably enhanced in angiogenesis VECs as compared to normal VECs, assessed by RT-PCR. The bioinformatics analysis found that the CarG element existed in the promoter region of AQP1 gene of many familiar mammals, including of mouse, rat, human etc. These results were the first to indicate that AQP1 was a target gene which could be regulated by MRTF-A/SRF.
机译:最近的研究表明,内皮细胞中Aquaporin1(AQP1)的表达在细胞迁移中发挥了重要作用,以及迁移相关细胞功能,如伤口愈合和中性粒细胞运动。在本研究中,我们提供了证据表明血管生成期间血管内皮细胞(VECs)中的AQP1表达与MRTF-A有关。形态学和免疫荧光测定证明来自正常和血管生成组织的VEC具有类似的外观。逆转录聚合酶链反应(RT-PCR),免疫印迹和免疫荧光分析认为,AQP1表达在血管生成VEC中显着高于正常VEC。与正常的VECs相比,MRTF-A表达在血管生成VEC中也显着增强,得到RT-PCR评估。生物信息学分析发现,在许多熟悉的哺乳动物的AQP1基因的启动子区中存在曲调元素,包括小鼠,大鼠,人类等。这些结果是第一个表明AQP1是靶基因,其可以由MRTF调节A / SRF。

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