• DocumentCode
    2499554
  • Title

    Aquaporin-1 Activity of Plasma Membrane Affects MCF-7 Mammary Carcinoma Cell Migration

  • Author

    Jiang, Yong ; Zhang, Xin ; Su, Rui ; Wang, Nan

  • Author_Institution
    Key Lab. of Ind. Microbiol., Tianjin Univ. of Sci. & Technol. Tianjin, Tianjin, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    Recent studies uncovered an important role of aquaporins in cell migration, and migration-associated cell function such as angiogenesis, wound healing, and neutrophil motility. Here we provide evidence that aquaporin expression is involved in MCF-7 human mammary carcinoma cell migration. Reverse transcription-polymerase chain reaction, immunoblot and immunofluorescence analysis demonstrated two populations of MCF-7 cell clones with low (MCF-7l) and high (MCF-7A) AQP1 expression and the AQP1 protein expression patterns in the plasma membrane of MCF-7 cells. MCF-7 cell clones (MCF-11 and MCF-7A) with low and about two-fold higher osmotic water permeability were identified by functional assays with corresponding low and high AQP1 expression. Cell migration rate was remarkably higher in MCF-7A cells as compared to MCF-7l cells, assessed by wound healing and Boyden chamber assays. Adenoviral-mediated AQP1 expression in MCF-7l cells increased their water permeability and migration rate to the level similar to MCF-7A cells. These results provide the direct evidence that aquaporin-mediated membrane water permeability enhances MCF-7 mammary carcinoma cell migration and may be associated with mammary carcinoma invasion and metastasis.
  • Keywords
    biomembranes; cancer; cell motility; enzymes; fluorescence; molecular biophysics; osmosis; permeability; proteins; tumours; AQP1 protein expression pattern; Boyden chamber assay; MCF-7 cell clone; MCF-7 human mammary carcinoma cell migration; adenoviral-mediated AQP1 expression; angiogenesis; aquaporin-1 activity; immunoblot; immunofluorescence analysis; neutrophil motility; reverse transcription-polymerase chain reaction; two-fold higher osmotic water permeability; wound healing; Biomembranes; Cloning; Humans; Immune system; Metastasis; Pattern analysis; Permeability; Plasmas; Proteins; Wounds;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5162404
  • Filename
    5162404