Get access
Journal of Cellular Biochemistry

The mechanism underlying the effects of the cell surface ATP synthase on the regulation of intracellular acidification during acidosis

Authors

  • Wen-juan Wang,

    1. Department of Laboratory Medicine, Shanghai Sixth People's Hospital of Shanghai, Shanghai JiaoTong University School of Medicine, Shanghai 200233, PR China
    Search for more papers by this author
  • Xiao-xing Shi,

    1. Department of Laboratory Medicine, Shanghai Wujing General Hospital, PR China
    Search for more papers by this author
  • Yi-wen Liu,

    1. Department of Laboratory Medicine, Shanghai Sixth People's Hospital of Shanghai, Shanghai JiaoTong University School of Medicine, Shanghai 200233, PR China
    Search for more papers by this author
  • Yi-qing He,

    1. Department of Laboratory Medicine, Shanghai Sixth People's Hospital of Shanghai, Shanghai JiaoTong University School of Medicine, Shanghai 200233, PR China
    Search for more papers by this author
  • Ying-zhi Wang,

    1. Department of Laboratory Medicine, Shanghai Sixth People's Hospital of Shanghai, Shanghai JiaoTong University School of Medicine, Shanghai 200233, PR China
    Search for more papers by this author
  • Cui-xia Yang,

    1. Department of Laboratory Medicine, Shanghai Sixth People's Hospital of Shanghai, Shanghai JiaoTong University School of Medicine, Shanghai 200233, PR China
    Search for more papers by this author
  • Feng Gao

    Corresponding author
    1. Department of Laboratory Medicine, Shanghai Sixth People's Hospital of Shanghai, Shanghai JiaoTong University School of Medicine, Shanghai 200233, PR China
    • Department of Laboratory Medicine, Shanghai Sixth People's Hospital of Shanghai, Shanghai JiaoTong University School of Medicine, 600 Yi-shan Road, Shanghai 200233, PR China.
    Search for more papers by this author

  • WenJuan Wang and Xiao-xing Shi contributed equally to this work.

Abstract

The F1F0 ATP synthase has recently become the focus of anti-cancer research. It was once thought that ATP synthases were located strictly on the inner mitochondrial membrane; however, in 1994, it was found that some ATP synthases localized to the cell surface. The cell surface ATP synthases are involved in angiogenesis, lipoprotein metabolism, innate immunity, hypertension, the regulation of food intake, and other processes. Inhibitors of this synthase have been reported to be cytotoxic and to induce intracellular acidification. However, the mechanisms by which these effects are mediated and the molecular pathways that are involved remain unclear. In this study, we aimed to determine whether the inhibition of cell proliferation and the induction of cell apoptosis that are induced by inhibitors of the cell surface ATP synthase are associated with intracellular acidification and to investigate the mechanism that underlines the effects of this inhibition, particularly in an acidic tumor environment. We demonstrated that intracellular acidification contributes to the cell proliferation inhibition that is mediated by cell surface ATP synthase inhibitors, but not to the induction of apoptosis. Intracellular acidification is only one of the mechanisms of ecto-ATP synthase-targeted antitumor drugs. We propose that intracellular acidification in combination with the inhibition of cell surface ATP generation induce cell apoptosis after cell surface ATP synthase blocked by its inhibitors. A better understanding of the mechanisms activated by ecto-ATP synthase-targeted cancer therapies may facilitate the development of potent anti-tumor therapies, which target this enzyme and do not exhibit clinical limitations. J. Cell. Biochem. 114: 1695–1703, 2013. © 2013 Wiley Periodicals, Inc.

Get access to the full text of this article

Ancillary