Literature DB >> 23097574

Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T.

Christopher R Bayliss1, Adam M Jacques, Man-Ching Leung, Douglas G Ward, Charles S Redwood, Clare E Gallon, O'Neal Copeland, William J McKenna, Cristobal Dos Remedios, Steven B Marston, Andrew E Messer.   

Abstract

AIMS: We studied the relationship between myofilament Ca(2+) sensitivity and troponin I (TnI) phosphorylation by protein kinase A at serines 22/23 in human heart troponin isolated from donor hearts and from myectomy samples from patients with hypertrophic obstructive cardiomyopathy (HOCM). METHODS AND
RESULTS: We used a quantitative in vitro motility assay. With donor heart troponin, Ca(2+) sensitivity is two- to three-fold higher when TnI is unphosphorylated. In the myectomy samples from patients with HOCM, the mean level of TnI phosphorylation was low: 0.38 ± 0.19 mol Pi/mol TnI compared with 1.60 ± 0.19 mol Pi/mol TnI in donor hearts, but no difference in myofilament Ca(2+) sensitivity was observed. Thus, troponin regulation of thin filament Ca(2+) sensitivity is abnormal in HOCM hearts. HOCM troponin (0.29 mol Pi/mol TnI) was treated with protein kinase A to increase the level of phosphorylation to 1.56 mol Pi/mol TnI. No difference in EC(50) was found in thin filaments containing high and low TnI phosphorylation levels. This indicates that Ca(2+) sensitivity is uncoupled from TnI phosphorylation in HOCM heart troponin. Coupling could be restored by replacing endogenous troponin T (TnT) with the recombinant TnT T3 isoform. No difference in Ca(2+) sensitivity was observed if TnI was exchanged into HOCM heart troponin or if TnT was exchanged into the highly phosphorylated donor heart troponin. Comparison of donor and HOCM heart troponin by mass spectrometry and with adduct-specific antibodies did not show any differences in TnT isoform expression, phosphorylation or any post-translational modifications.
CONCLUSION: An abnormality in TnT is responsible for uncoupling myofibrillar Ca(2+) sensitivity from TnI phosphorylation in the septum of HOCM patients.

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Year:  2012        PMID: 23097574     DOI: 10.1093/cvr/cvs322

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  23 in total

1.  Pathogenesis associated with a restrictive cardiomyopathy mutant in cardiac troponin T is due to reduced protein stability and greatly increased myofilament Ca2+ sensitivity.

Authors:  Michelle S Parvatiyar; Jose Renato Pinto
Journal:  Biochim Biophys Acta       Date:  2014-11-01

2.  Best Practice BioBanking of Human Heart Tissue.

Authors:  Sean Lal; Amy Li; David Allen; Paul D Allen; Paul Bannon; Tim Cartmill; Roger Cooke; Alan Farnsworth; Anne Keogh; Cristobal Dos Remedios
Journal:  Biophys Rev       Date:  2015-11-02

3.  Long term ablation of protein kinase A (PKA)-mediated cardiac troponin I phosphorylation leads to excitation-contraction uncoupling and diastolic dysfunction in a knock-in mouse model of hypertrophic cardiomyopathy.

Authors:  David Dweck; Marcos A Sanchez-Gonzalez; Audrey N Chang; Raul A Dulce; Crystal-Dawn Badger; Andrew P Koutnik; Edda L Ruiz; Brittany Griffin; Jingsheng Liang; Mohamed Kabbaj; Frank D Fincham; Joshua M Hare; J Michael Overton; Jose R Pinto
Journal:  J Biol Chem       Date:  2014-06-27       Impact factor: 5.157

4.  Uncoupling of myofilament Ca2+ sensitivity from troponin I phosphorylation by mutations can be reversed by epigallocatechin-3-gallate.

Authors:  Maria Papadaki; Petr G Vikhorev; Steven B Marston; Andrew E Messer
Journal:  Cardiovasc Res       Date:  2015-06-24       Impact factor: 10.787

5.  Z-band alternatively spliced PDZ motif protein (ZASP) is the major O-linked β-N-acetylglucosamine-substituted protein in human heart myofibrils.

Authors:  Man-Ching Leung; Paul G Hitchen; Douglas G Ward; Andrew E Messer; Steven B Marston
Journal:  J Biol Chem       Date:  2012-12-27       Impact factor: 5.157

6.  The dilated cardiomyopathy-causing mutation ACTC E361G in cardiac muscle myofibrils specifically abolishes modulation of Ca(2+) regulation by phosphorylation of troponin I.

Authors:  Petr G Vikhorev; Weihua Song; Ross Wilkinson; O'Neal Copeland; Andrew E Messer; Michael A Ferenczi; Steven B Marston
Journal:  Biophys J       Date:  2014-11-18       Impact factor: 4.033

7.  Computational modeling of Takotsubo cardiomyopathy: effect of spatially varying β-adrenergic stimulation in the rat left ventricle.

Authors:  Sander Land; Steven A Niederer; William E Louch; Åsmund T Røe; Jan Magnus Aronsen; Daniel J Stuckey; Markus B Sikkel; Matthew H Tranter; Alexander R Lyon; Sian E Harding; Nicolas P Smith
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-09-19       Impact factor: 4.733

8.  TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype.

Authors:  M Papadaki; J M de Winter; M B Neu; S Donkervoort; J Kirschner; V Bolduc; M L Yang; M A Gibbons; Y Hu; J Dastgir; M E Leach; A Rutkowski; A R Foley; M Krüger; E P Wartchow; E McNamara; R Ong; K J Nowak; N G Laing; N F Clarke; Cac Ottenheijm; S B Marston; C G Bönnemann
Journal:  Ann Neurol       Date:  2015-11-13       Impact factor: 10.422

9.  OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency.

Authors:  Steven Marston; Cecile Montgiraud; Alex B Munster; O'Neal Copeland; Onjee Choi; Cristobal Dos Remedios; Andrew E Messer; Elisabeth Ehler; Ralph Knöll
Journal:  PLoS One       Date:  2015-09-25       Impact factor: 3.240

Review 10.  Investigating the role of uncoupling of troponin I phosphorylation from changes in myofibrillar Ca(2+)-sensitivity in the pathogenesis of cardiomyopathy.

Authors:  Andrew E Messer; Steven B Marston
Journal:  Front Physiol       Date:  2014-08-25       Impact factor: 4.566

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