Journal of Molecular and Cellular Cardiology
Volume 52, Issue 5 , Pages 1145-1154, May 2012

The dynamic role of cardiac myosin binding protein-C during ischemia

  • Robert S. Decker

      Affiliations

    • Feinberg Cardiovascular Research Institute, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
    • Feinberg Cardiovascular Research Institute, Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
  • ,
  • Sakie Nakamura

      Affiliations

    • Feinberg Cardiovascular Research Institute, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
  • ,
  • Marlene L. Decker

      Affiliations

    • Feinberg Cardiovascular Research Institute, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
  • ,
  • Mareike Sausamuta

      Affiliations

    • University of Jena, Jena Germany
  • ,
  • Sammy Sinno

      Affiliations

    • Feinberg Cardiovascular Research Institute, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
  • ,
  • Kathleen Harris

      Affiliations

    • Feinberg Cardiovascular Research Institute, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
  • ,
  • Francis J. Klocke

      Affiliations

    • Feinberg Cardiovascular Research Institute, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
  • ,
  • Irina Kulikovskaya

      Affiliations

    • Department of Physiology School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6085, USA
  • ,
  • Saul Winegrad

      Affiliations

    • Department of Physiology School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6085, USA
    • Corresponding Author InformationCorresponding author at: Department of Physiology School of Medicine University of Pennsylvania Philadelphia, PA 19104-6085, USA. Tel.: +1 215 898 7017; fax: +1 215 573 5851.

Received 29 November 2011; received in revised form 5 January 2012; accepted 6 January 2012. published online 19 January 2012.

Abstract 

Cardiac myosin binding protein C (cMyBP-C) is a myofibrillar protein important for normal myocardial contractility and stability. In mutated form it can cause cardiomyopathy and heart failure. cMyBP-C appears to have separate regions for different functions. Three phosphorylation sites near the N terminus modulate contractility by their effect on both the kinetics of contraction and the binding site of the N-terminus. The C terminal region binds to myosin rods and stabilizes thick filament structure.

The aim of the study reported here was to test whether cMyBPC is important in producing the structural and functional changes that result from ischemia/reperfusion. In this study the sequential changes in cMyBP-C, contractility, and thick filament structure following dephosphorylation of cMyBP-C associated with ischemia and reperfusion have been studied in biopsied specimens from chronically instrumented dogs. One and two dimensional electrophoresis, electron microscopy and immunocytochemistry with multiple antibodies generated against different domains in cMyBP-C have been used to follow structural changes in cMyBP-C. Ischemia produced dephosphorylation of cMyBP-C. Subsequent reperfusion released the dephosphorylated cMyBP-C from myofibrils and activated proteolysis of the cytoplasmic cMyBP-C. This in turn leads to increased vulnerability of cMyBP-C to proteolysis and increased degradation of thick filaments. The state of cMyBP-C appears to be closely related to phosphorylation and dephosphorylation of serine 282. In the absence of the stabilizing action of cMyBP-C either as a consequence of genetic mutation or dephosphorylation, premature degradation of thick filaments occurs and is accompanied by persistent contractile dysfunction.

Highlights

► Ischemia of the heart dephosphorylates cMyBP-C bound to myofibrils. ► Reperfusion releases dephosphorylated cMyBP-C from myofibrils. ► Reperfusion activates proteolysis of the cytoplasmic cMyBP-C. ► Increased degradation of thick filaments follows proteolysis of cMyBP-C. ► Phosphorylation of serine 282 and the state of cMyBP-C change in parallel.

Abbreviations: cMyBP-C, Cardiac myosin-binding protein C, LCx, left coronary circumflex artery (occluded artery), LCxM, myocardium fed by LCx, LAD, Left anterior descending coronary artery (normally perfused artery), NM, normally perfused myocardium, IM, ischemic myocardium, FWI, low flow ischemia, LC, left circumflex artery

Keywords: Myosin binding protein C, Cardiac ischemia, Phosphorylation, Cardiac contractility, Thick filament

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PII: S0022-2828(12)00035-1

doi:10.1016/j.yjmcc.2012.01.006

Journal of Molecular and Cellular Cardiology
Volume 52, Issue 5 , Pages 1145-1154, May 2012