Literature DB >> 3417854

Skinned ventricular fibres: troponin C extraction is species-dependent and its replacement with skeletal troponin C changes Sr2+ activation properties.

P E Hoar1, J D Potter, W G Kerrick.   

Abstract

Troponin C (TnC) was extracted from bundles of rat and mouse skinned cardiac ventricular cells by a method similar to that previously used to extract TnC from skinned rabbit skeletal muscle cells (Kerrick et al., J. biol. Chem. 260, 15687-93, 1985) and replaced with either bovine cardiac or rabbit fast-twitch skeletal TnC. In contrast, the same TnC extraction conditions will not extract TnC from either bovine or rabbit cardiac skinned fibres. When the extracted TnC was replaced by bovine cardiac TnC the Sr2+-activated tension relationship was not altered from control values. In contrast, replacement of the endogenous TnC with exogenous rabbit fast-twitch TnC caused the relationship between Sr2+ concentration and tension to shift towards higher concentrations of Sr2+. The Sr2+-activated tension of rat fibres with fast-twitch TnC was identical to that of rabbit fast-twitch skinned fibres. Partial skeletal TnC substitution in skinned cardiac cells gradually shifted the relationship between tension and [Sr2+] to higher Sr2+ concentrations and caused the cells to be activated over a wider range of Sr2+ concentrations. Thus it appears that the activation of rat cardiac skinned cells by Sr2+ is determined by characteristics of the TnC. In contrast, the Sr2+ activation of skinned rabbit fast-twitch skeletal fibres containing either cardiac or skeletal TnC is identical, strongly suggesting that protein-protein interactions determined the Sr2+ -activation properties in these fibres.

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Year:  1988        PMID: 3417854     DOI: 10.1007/BF01773738

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  22 in total

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Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

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Authors:  W G Kerrick; B Krasner
Journal:  J Appl Physiol       Date:  1975-12       Impact factor: 3.531

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Journal:  Biochem J       Date:  1981-04-01       Impact factor: 3.857

4.  The calcium and magnesium binding sites on cardiac troponin and their role in the regulation of myofibrillar adenosine triphosphatase.

Authors:  M J Holroyde; S P Robertson; J D Johnson; R J Solaro; J D Potter
Journal:  J Biol Chem       Date:  1980-12-25       Impact factor: 5.157

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Authors:  P C Leavis; E L Kraft
Journal:  Arch Biochem Biophys       Date:  1978-03       Impact factor: 4.013

6.  Preparation of troponin and its subunits.

Authors:  J D Potter
Journal:  Methods Enzymol       Date:  1982       Impact factor: 1.600

7.  Alternate model for the cooperative equilibrium binding of myosin subfragment-1-nucleotide complex to actin-troponin-tropomyosin.

Authors:  T L Hill; E Eisenberg; L E Greene
Journal:  Proc Natl Acad Sci U S A       Date:  1983-01       Impact factor: 11.205

8.  Force measurements in skinned muscle fibres.

Authors:  D C Hellam; R J Podolsky
Journal:  J Physiol       Date:  1969-02       Impact factor: 5.182

9.  The control of myocardial contraction with skeletal fast muscle troponin C.

Authors:  A Babu; S P Scordilis; E H Sonnenblick; J Gulati
Journal:  J Biol Chem       Date:  1987-04-25       Impact factor: 5.157

10.  The effects of partial extraction of TnC upon the tension-pCa relationship in rabbit skinned skeletal muscle fibers.

Authors:  R L Moss; G G Giulian; M L Greaser
Journal:  J Gen Physiol       Date:  1985-10       Impact factor: 4.086

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  11 in total

1.  The role of the Ca(2+) regulatory sites of skeletal troponin C in modulating muscle fibre reactivity to the Ca(2+) sensitizer bepridil.

Authors:  P Kischel; B Bastide; J D Potter; Y Mounier
Journal:  Br J Pharmacol       Date:  2000-12       Impact factor: 8.739

2.  The low-affinity Ca2(+)-binding sites in cardiac/slow skeletal muscle troponin C perform distinct functions: site I alone cannot trigger contraction.

Authors:  H L Sweeney; R M Brito; P R Rosevear; J A Putkey
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

3.  Changes in contractile activation characteristics of rat fast and slow skeletal muscle fibres during regeneration.

Authors:  Paul Gregorevic; David R Plant; Nicole Stupka; Gordon S Lynch
Journal:  J Physiol       Date:  2004-06-04       Impact factor: 5.182

4.  Calcium and strontium activation characteristics of muscle fibres: a comment.

Authors:  A Babu; E Sonnenblick; J Gulati
Journal:  J Muscle Res Cell Motil       Date:  1991-02       Impact factor: 2.698

5.  Pyrene-labeled cardiac troponin C. Effect of Ca2+ on monomer and excimer fluorescence in solution and in myofibrils.

Authors:  Y M Liou; F Fuchs
Journal:  Biophys J       Date:  1992-04       Impact factor: 4.033

6.  Calcium and strontium activation characteristics of skeletal muscle fibres from the small marsupial Sminthopsis macroura.

Authors:  G J Wilson; D G Stephenson
Journal:  J Muscle Res Cell Motil       Date:  1990-02       Impact factor: 2.698

7.  Effects of the constitutively active proteolytic fragment of protein kinase C on the contractile properties of demembranated smooth muscle fibres.

Authors:  J E Parente; M P Walsh; W G Kerrick; P E Hoar
Journal:  J Muscle Res Cell Motil       Date:  1992-02       Impact factor: 2.698

8.  Skeletal troponin C reduces contractile sensitivity to acidosis in cardiac myocytes from transgenic mice.

Authors:  J M Metzger; M S Parmacek; E Barr; K Pasyk; W I Lin; K L Cochrane; L J Field; J M Leiden
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-01       Impact factor: 11.205

9.  The role of troponin C in the length dependence of Ca(2+)-sensitive force of mammalian skeletal and cardiac muscles.

Authors:  J Gulati; E Sonnenblick; A Babu
Journal:  J Physiol       Date:  1991-09       Impact factor: 5.182

10.  Length dependence of Ca2+ sensitivity of tension in mouse cardiac myocytes expressing skeletal troponin C.

Authors:  K S McDonald; L J Field; M S Parmacek; M Soonpaa; J M Leiden; R L Moss
Journal:  J Physiol       Date:  1995-02-15       Impact factor: 5.182

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