Literature DB >> 10677358

Ca2+ buffering in the heart: Ca2+ binding to and activation of cardiac myofibrils.

G A Smith1, H B Dixon, H L Kirschenlohr, A A Grace, J C Metcalfe, J I Vandenberg.   

Abstract

The measurement of cardiac Ca(2+) transients using spectroscopic Ca(2+) indicators is significantly affected by the buffering properties of the indicators. The aim of the present study was to construct a model of cardiac Ca(2+) buffering that satisfied the kinetic constraints imposed by the maximum attainable rates of cardiac contraction and relaxation on the Ca(2+) dissociation rate constants and which would account for the observed effects of (19)F-NMR indicators on the cardiac Ca(2+) transient in the Langendorff-perfused ferret heart. It is generally assumed that the Ca(2+) dependency of myofibril activation in cardiac myocytes is mediated by a single Ca(2+)-binding site on troponin C. A model based on 1:1 Ca(2+) binding to the myofilaments, however, was unable to reproduce our experimental data, but a model in which we assumed ATP-dependent co-operative Ca(2+) binding to the myofilaments was able to reproduce these data. This model was used to calculate the concentration and dissociation constant of the ATP-independent myofilament Ca(2+) binding, giving 58 and 2.0 microM respectively. In addition to reproducing our experimental data on the concentration of free Ca(2+) ions in the cytoplasm ([Ca(2+)](i)), the resulting Ca(2+) and ATP affinities given by fitting of the model also provided good predictions of the Ca(2+) dependence of the myofibrillar ATPase activity measured under in vitro conditions. Solutions to the model also indicate that the Ca(2+) mobilized during each beat remains unchanged in the presence of the additional buffering load from Ca(2+) indicators. The new model was used to estimate the extent of perturbation of the Ca(2+) transient caused by different concentrations of indicators. As little as 10 microM of a Ca(2+) indicator with a dissociation constant of 200 nM will cause a 20% reduction in peak-systolic [Ca(2+)](i) and 30 microM will cause approx. 50% reduction in the peak-systolic [Ca(2+)](i) in a heart paced at 1.0 Hz.

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Year:  2000        PMID: 10677358      PMCID: PMC1220865     

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  37 in total

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Journal:  J Biochem       Date:  1977-09       Impact factor: 3.387

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Authors:  T R Shannon; D M Bers
Journal:  Biophys J       Date:  1997-09       Impact factor: 4.033

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Journal:  J Gen Physiol       Date:  1996-11       Impact factor: 4.086

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Journal:  Circ Res       Date:  1974-04       Impact factor: 17.367

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Journal:  Biophys J       Date:  1994-10       Impact factor: 4.033

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Journal:  J Mol Biol       Date:  1980-06-05       Impact factor: 5.469

8.  Estimation of systolic and diastolic free intracellular Ca2+ by titration of Ca2+ buffering in the ferret heart.

Authors:  H L Kirschenlohr; A A Grace; J I Vandenberg; J C Metcalfe; G A Smith
Journal:  Biochem J       Date:  2000-03-01       Impact factor: 3.857

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Journal:  J Biol Chem       Date:  1996-01-12       Impact factor: 5.157

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Journal:  Biochem J       Date:  1976-11       Impact factor: 3.857

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  4 in total

1.  The effect of Mg2+ on cardiac muscle function: Is CaATP the substrate for priming myofibril cross-bridge formation and Ca2+ reuptake by the sarcoplasmic reticulum?

Authors:  G A Smith; J I Vandenberg; N S Freestone; H B Dixon
Journal:  Biochem J       Date:  2001-03-15       Impact factor: 3.857

Review 2.  Alpha-tropomyosin mutations in inherited cardiomyopathies.

Authors:  Charles Redwood; Paul Robinson
Journal:  J Muscle Res Cell Motil       Date:  2013-09-05       Impact factor: 2.698

Review 3.  Current insights into LMNA cardiomyopathies: Existing models and missing LINCs.

Authors:  Daniel Brayson; Catherine M Shanahan
Journal:  Nucleus       Date:  2017-01-02       Impact factor: 4.197

4.  Hypertrophic cardiomyopathy mutations increase myofilament Ca2+ buffering, alter intracellular Ca2+ handling, and stimulate Ca2+-dependent signaling.

Authors:  Paul Robinson; Xing Liu; Alexander Sparrow; Suketu Patel; Yin-Hua Zhang; Barbara Casadei; Hugh Watkins; Charles Redwood
Journal:  J Biol Chem       Date:  2018-05-14       Impact factor: 5.157

  4 in total

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