• DocumentCode
    3130611
  • Title

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

  • Author

    Jiang, Yong ; Sun, Zhe ; Qiang, Meng-meng ; Su, Rui ; Guo, Yu-ting ; Luo, Xue-Gang ; Wang, Nan ; Zhang, Tong-Cun

  • Author_Institution
    Key Lab. of Ind. Microbiol., Minist. of Educ., Tianjin, China
  • fYear
    2010
  • fDate
    18-20 June 2010
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    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.
  • Keywords
    bioinformatics; biomembrane transport; blood vessels; cell motility; fluorescence; genetics; molecular biophysics; proteins; AQP1 expression; CarG element; MRTF-A; angiogenesis tissues; aquaporin1; bioinformatics analysis; cell function; cell migration; gene; immunoblot analysis; immunofluorescence assay; morphology; myocardin-related transcription factors; neutrophil motility; reverse transcription-polymerase chain reaction; vascular endothelia cells; wound healing; Bioinformatics; Heart; Humans; Immune system; Laboratories; Mice; Morphology; Muscles; RNA; Wounds;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
  • Conference_Location
    Chengdu
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-4712-1
  • Electronic_ISBN
    2151-7614
  • Type

    conf

  • DOI
    10.1109/ICBBE.2010.5516901
  • Filename
    5516901