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Rationally engineered Troponin C modulates in vivo cardiac function and performance in health and disease

Author

Listed:
  • Vikram Shettigar

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Bo Zhang

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology
    Present address: Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China)

  • Sean C. Little

    (Bristol-Myers Squibb)

  • Hussam E. Salhi

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Brian J. Hansen

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Ning Li

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Jianchao Zhang

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Steve R. Roof

    (Q-Test Labs)

  • Hsiang-Ting Ho

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Lucia Brunello

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Jessica K. Lerch

    (Center for Brain and Spinal Cord Repair, The Ohio State University College of Medicine)

  • Noah Weisleder

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Vadim V. Fedorov

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Federica Accornero

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Jill A. Rafael-Fortney

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Sandor Gyorke

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Paul M. L. Janssen

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Brandon J. Biesiadecki

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Mark T. Ziolo

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

  • Jonathan P. Davis

    (Davis Heart and Lung Research Institute and Department of Physiology and Cell Biology)

Abstract

Treatment for heart disease, the leading cause of death in the world, has progressed little for several decades. Here we develop a protein engineering approach to directly tune in vivo cardiac contractility by tailoring the ability of the heart to respond to the Ca2+ signal. Promisingly, our smartly formulated Ca2+-sensitizing TnC (L48Q) enhances heart function without any adverse effects that are commonly observed with positive inotropes. In a myocardial infarction (MI) model of heart failure, expression of TnC L48Q before the MI preserves cardiac function and performance. Moreover, expression of TnC L48Q after the MI therapeutically enhances cardiac function and performance, without compromising survival. We demonstrate engineering TnC can specifically and precisely modulate cardiac contractility that when combined with gene therapy can be employed as a therapeutic strategy for heart disease.

Suggested Citation

  • Vikram Shettigar & Bo Zhang & Sean C. Little & Hussam E. Salhi & Brian J. Hansen & Ning Li & Jianchao Zhang & Steve R. Roof & Hsiang-Ting Ho & Lucia Brunello & Jessica K. Lerch & Noah Weisleder & Vadi, 2016. "Rationally engineered Troponin C modulates in vivo cardiac function and performance in health and disease," Nature Communications, Nature, vol. 7(1), pages 1-13, April.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10794
    DOI: 10.1038/ncomms10794
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