LETM1‐dependent mitochondrial Ca <sup>2+</sup> flux modulates cellular bioenergetics and proliferation

  • Patrick J. Doonan
    Department of Biochemistry Temple University School of Medicine Philadelphia Pennsylvania USA
  • Harish C. Chandramoorthy
    Department of Biochemistry Temple University School of Medicine Philadelphia Pennsylvania USA
  • Nicholas E. Hoffman
    Department of Biochemistry Temple University School of Medicine Philadelphia Pennsylvania USA
  • Xueqian Zhang
    Center for Translational Medicine Temple University School of Medicine Philadelphia Pennsylvania USA
  • César Cárdenas
    Anatomy and Developmental Biology Program Institute of Biomedical Sciences University of Chile Santiago Chile
  • Santhanam Shanmughapriya
    Department of Biochemistry Temple University School of Medicine Philadelphia Pennsylvania USA
  • Sudarsan Rajan
    Department of Biochemistry Temple University School of Medicine Philadelphia Pennsylvania USA
  • Sandhya Vallem
    Department of Biochemistry Temple University School of Medicine Philadelphia Pennsylvania USA
  • Xiongwen Chen
    Cardiovascular Research Center Temple University School of Medicine Philadelphia Pennsylvania USA
  • J. Kevin Foskett
    Department of Physiology University of Pennsylvania Philadelphia Pennsylvania USA
  • Joseph Y. Cheung
    Center for Translational Medicine Temple University School of Medicine Philadelphia Pennsylvania USA
  • Steven R. Houser
    Cardiovascular Research Center Temple University School of Medicine Philadelphia Pennsylvania USA
  • Muniswamy Madesh
    Department of Biochemistry Temple University School of Medicine Philadelphia Pennsylvania USA

書誌事項

公開日
2014-07-30
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1096/fj.14-256453
公開者
Wiley

この論文をさがす

説明

<jats:p> Dysregulation of mitochondrial Ca <jats:sup>2+</jats:sup> ‐dependent bioenergetics has been implicated in various pathophysiological settings, including neurodegeneration and myocardial infarction. Although mitochondrial Ca <jats:sup>2+</jats:sup> transport has been characterized, and several molecules, including LETM1, have been identified, the functional role of LETM1‐mediated Ca <jats:sup>2+</jats:sup> transport remains unresolved. This study examines LETM1‐mediated mitochondrial Ca <jats:sup>2+</jats:sup> transport and bioenergetics in multiple cell types, including fibroblasts derived from patients with Wolf‐Hirschhorn syndrome (WHS). The results show that both mitochondrial Ca <jats:sup>2+</jats:sup> influx and efflux rates are impaired in LETM1 knockdown, and similar phenotypes were observed in ΔEF hand, <jats:sup>D676A D688K</jats:sup> LETM1 mutant‐overexpressed cells, and in cells derived from patients with WHS. Although LETM1 levels were lower in WHS‐derived fibroblasts, the mitochondrial Ca <jats:sup>2+</jats:sup> uniporter components MCU, MCUR1, and MICU1 remain unaltered. In addition, the MCU mitoplast patch‐clamp current ( <jats:italic>I</jats:italic> <jats:sub>MCU</jats:sub> ) was largely unaffected in LETM1‐knockdown cells. Silencing of LETM1 also impaired basal mitochondrial oxygen consumption, possibly <jats:italic>via</jats:italic> complex IV inactivation and ATP production. Remarkably, LETM1 knockdown also resulted in increased reactive oxygen species production. Further, LETM1 silencing promoted AMPK activation, autophagy, and cell cycle arrest. Reconstitution of LETM1 or antioxidant overexpression rescued mitochondrial Ca <jats:sup>2+</jats:sup> transport and bioenergetics. These findings reveal the role of LETM1‐dependent mitochondrial Ca <jats:sup>2+</jats:sup> flux in shaping cellular bioenergetics.—Doonan, P J., Chandramoorthy, H. C., Hoffman, N. E., Zhang, X., Cárdenas, C., Shanmughapriya, S., Rajan, S., Vallem, S., Chen, X., Foskett, J. K., Cheung, J. Y., Houser, S. R., Madesh, M., LETM1‐dependent mitochondrial Ca2+ flux modulates cellular bioenergetics and proliferation. FASEB J. 28, 4936–4949 (2014). <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://www.fasebj.org">www.fasebj.org</jats:ext-link> </jats:p>

収録刊行物

被引用文献 (3)*注記

もっと見る

問題の指摘

ページトップへ