Literature DB >> 8478423

Lack of dystrophin but normal calcium homeostasis in smooth muscle from dystrophic mdx mice.

B Boland1, B Himpens, R Casteels, J M Gillis.   

Abstract

The free cytosolic Ca2+ concentration ([Ca2+]i) in the dystrophin-lacking smooth muscle from mdx mice was studied to gain new insights into the relation between dystrophin and cytoplasmic Ca2+ homeostasis, which was reported to be impaired in the mdx skeletal muscle. We observed that [Ca2+]i, as measured with the fluorescent Ca2+ indicator fura-2, was not elevated in resting smooth muscle of the vas deferens from mdx mice, in comparison with control C57 mice. Changes of the external Ca2+ concentration evoked similar changes of [Ca2+]i in mdx and control vas deferens. During contraction, cytosolic Ca2+ transients were identical, both in amplitude and in kinetics, whether or not dystrophin was present. Stretches evoked similar Ca2+ increases in muscles from both strains. Intracellular Ca2+ homeostasis appears to be unimpaired in mdx smooth muscle. Thus, the lack of dystrophin per se does not automatically induce a perturbation of Ca metabolism in muscle cells.

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Year:  1993        PMID: 8478423     DOI: 10.1007/bf00132187

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


  30 in total

1.  Developmental regulation of mechanosensitive calcium channels in skeletal muscle from normal and mdx mice.

Authors:  C M Haws; J B Lansman
Journal:  Proc Biol Sci       Date:  1991-09-23       Impact factor: 5.349

Review 2.  Molecular genetics of Duchenne and Becker muscular dystrophy.

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Journal:  Gastroenterology       Date:  1986-02       Impact factor: 22.682

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Authors:  N Ambache; M A Zar
Journal:  J Physiol       Date:  1971-07       Impact factor: 5.182

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Journal:  Gastroenterology       Date:  1982-04       Impact factor: 22.682

6.  Relationship between force and Ca2+ in anococcygeal and vas deferens smooth muscle cells of the mouse.

Authors:  B Boland; B Himpens; J M Gillis; R Casteels
Journal:  Pflugers Arch       Date:  1992-05       Impact factor: 3.657

7.  Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin.

Authors:  P Y Fong; P R Turner; W F Denetclaw; R A Steinhardt
Journal:  Science       Date:  1990-11-02       Impact factor: 47.728

8.  Small-caliber skeletal muscle fibers do not suffer deleterious consequences of dystrophic gene expression.

Authors:  G Karpati; S Carpenter
Journal:  Am J Med Genet       Date:  1986-12

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Authors:  M Koenig; A P Monaco; L M Kunkel
Journal:  Cell       Date:  1988-04-22       Impact factor: 41.582

10.  Possible systemic smooth muscle layer dysfunction due to a deficiency of dystrophin in Duchenne muscular dystrophy.

Authors:  M Miyatake; T Miike; J Zhao; K Yoshioka; M Uchino; G Usuku
Journal:  J Neurol Sci       Date:  1989-10       Impact factor: 3.181

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  3 in total

Review 1.  Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse.

Authors:  J M Gillis
Journal:  J Muscle Res Cell Motil       Date:  1999-10       Impact factor: 2.698

2.  Cellular mechanism underlying the facilitation of contractile response of vas deferens smooth muscle by sodium orthovanadate.

Authors:  Lei Zhao; Zhe Wang; Ye-Chun Ruan; Wen-Liang Zhou
Journal:  Mol Cell Biochem       Date:  2012-04-04       Impact factor: 3.396

Review 3.  The dystrophin superfamily: variability and complexity.

Authors:  E Fabbrizio; F Pons; A Robert; G Hugon; A Bonet-Kerrache; D Mornet
Journal:  J Muscle Res Cell Motil       Date:  1994-12       Impact factor: 2.698

  3 in total

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