Literature DB >> 11454955

Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes.

N Imbert1, C Vandebrouck, G Duport, G Raymond, A A Hassoni, B Constantin, M J Cullen, C Cognard.   

Abstract

1. The goal of the present study was to investigate differences in calcium movements between normal and Duchenne muscular dystrophy (DMD) human contracting myotubes co-cultured with explants of rat spinal cord with attached dorsal root ganglia. Membrane potential, variations of intracellular calcium concentration and T- and L-type calcium currents were recorded. Further, a descriptive and quantitative study by electron microscopy of the ultrastructure of the co-cultures was carried out. 2. The resting membrane potential was slightly less negative in DMD (-61.4 +/- 1.1 mV) than in normal myotubes (-65.5 +/- 0.9 mV). Both types of myotube displayed spontaneous action potentials (mean firing frequency, 0.42 and 0.16 Hz, respectively), which triggered spontaneous calcium transients measured with Indo-1. 3. The time integral under the spontaneous Ca(2+) transients was significantly greater in DMD myotubes (97 +/- 8 nM s) than in normal myotubes (67 +/- 13 nM s). 4. The L- and T-type current densities estimated from patch-clamp recordings were smaller in DMD cells (2.0 +/- 0.5 and 0.90 +/- 0.19 pA pF(-1), respectively) than in normal cells (3.9 +/- 0.7 and 1.39 +/- 0.30 pA pF(-1), respectively). 5. The voltage-dependent inactivation relationships revealed a shift in the conditioning potential at which inactivation is half-maximal (V(h,0.5)) of the T- and L-type currents towards less negative potentials, from -72.1 +/- 0.7 and -53.7 +/- 1.5 mV in normal cells to -61.9 +/- 1.4 and -29.2 +/- 1.4 mV in DMD cells, respectively. 6. Both descriptive and quantitative studies by electron microscopy suggested a more advanced development of DMD myotubes as compared to normal ones. This conclusion was supported by the significantly larger capacitance of the DMD myotubes (408 +/- 45 pF) than of the normal myotubes (299 +/- 34 pF) of the same apparent size. 7. Taken together, these results show that differences in T- and L-type calcium currents between normal and DMD myotubes cannot simply explain all observed alterations in calcium homeostasis in DMD myotubes, thus suggesting that other transmembrane calcium transport mechanisms must also be altered in DMD myotubes compared with normal myotubes.

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Year:  2001        PMID: 11454955      PMCID: PMC2278716          DOI: 10.1111/j.1469-7793.2001.00343.x

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  25 in total

1.  Calcium currents in normal and dystrophic human skeletal muscle cells in culture.

Authors:  M Rivet; C Cognard; Y Rideau; G Duport; G Raymond
Journal:  Cell Calcium       Date:  1990-09       Impact factor: 6.817

2.  Cationic channels in normal and dystrophic human myotubes.

Authors:  C Vandebrouck; G Duport; C Cognard; G Raymond
Journal:  Neuromuscul Disord       Date:  2001-01       Impact factor: 4.296

3.  Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.

Authors:  O P Hamill; A Marty; E Neher; B Sakmann; F J Sigworth
Journal:  Pflugers Arch       Date:  1981-08       Impact factor: 3.657

4.  A new generation of Ca2+ indicators with greatly improved fluorescence properties.

Authors:  G Grynkiewicz; M Poenie; R Y Tsien
Journal:  J Biol Chem       Date:  1985-03-25       Impact factor: 5.157

5.  Dystrophin: the protein product of the Duchenne muscular dystrophy locus.

Authors:  E P Hoffman; R H Brown; L M Kunkel
Journal:  Cell       Date:  1987-12-24       Impact factor: 41.582

6.  The effect of methylprednisolone on intracellular calcium of normal and dystrophic human skeletal muscle cells.

Authors:  C Vandebrouck; N Imbert; G Duport; C Cognard; G Raymond
Journal:  Neurosci Lett       Date:  1999-07-09       Impact factor: 3.046

7.  Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface.

Authors:  E Bonilla; C E Samitt; A F Miranda; A P Hays; G Salviati; S DiMauro; L M Kunkel; E P Hoffman; L P Rowland
Journal:  Cell       Date:  1988-08-12       Impact factor: 41.582

8.  A third type of calcium current in cultured human skeletal muscle cells.

Authors:  M Rivet; C Cognard; N Imbert; Y Rideau; G Duport; G Raymond
Journal:  Neurosci Lett       Date:  1992-04-13       Impact factor: 3.046

9.  Human muscle cultured in monolayer and cocultured with fetal rat spinal cord: importance of dorsal root ganglia for achieving successful functional innervation.

Authors:  T Kobayashi; V Askanas; W K Engel
Journal:  J Neurosci       Date:  1987-10       Impact factor: 6.167

10.  Human myotube differentiation in vitro in different culture conditions.

Authors:  C Delaporte; B Dautreaux; M Fardeau
Journal:  Biol Cell       Date:  1986       Impact factor: 4.458

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  15 in total

Review 1.  Low-voltage-activated ("T-Type") calcium channels in review.

Authors:  Anne Marie R Yunker; Maureen W McEnery
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2.  Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes.

Authors:  Thomas M Suchyna; Frederick Sachs
Journal:  J Physiol       Date:  2007-01-25       Impact factor: 5.182

Review 3.  New insights in the regulation of calcium transfers by muscle dystrophin-based cytoskeleton: implications in DMD.

Authors:  Bruno Constantin; Stéphane Sebille; Christian Cognard
Journal:  J Muscle Res Cell Motil       Date:  2006-08-04       Impact factor: 2.698

Review 4.  The role of in vivo Ca²⁺ signals acting on Ca²⁺-calmodulin-dependent proteins for skeletal muscle plasticity.

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Journal:  J Physiol       Date:  2011-09-12       Impact factor: 5.182

5.  Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle.

Authors:  O Friedrich; M Both; C Weber; S Schürmann; M D H Teichmann; F von Wegner; R H A Fink; M Vogel; J S Chamberlain; C Garbe
Journal:  Biophys J       Date:  2010-02-17       Impact factor: 4.033

6.  Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice.

Authors:  O Friedrich; M Both; J M Gillis; J S Chamberlain; R H A Fink
Journal:  J Physiol       Date:  2003-10-31       Impact factor: 5.182

7.  Regulation of TRPC1 and TRPC4 cation channels requires an alpha1-syntrophin-dependent complex in skeletal mouse myotubes.

Authors:  Jessica Sabourin; Coralie Lamiche; Aurelie Vandebrouck; Christophe Magaud; Jerome Rivet; Christian Cognard; Nicolas Bourmeyster; Bruno Constantin
Journal:  J Biol Chem       Date:  2009-10-07       Impact factor: 5.157

8.  Functional classification of skeletal muscle networks. II. Applications to pathophysiology.

Authors:  Yu Wang; Jack Winters; Shankar Subramaniam
Journal:  J Appl Physiol (1985)       Date:  2012-10-18

9.  Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression.

Authors:  Martin D H Teichmann; Frederic V Wegner; Rainer H A Fink; Jeffrey S Chamberlain; Bradley S Launikonis; Boris Martinac; Oliver Friedrich
Journal:  PLoS One       Date:  2008-11-04       Impact factor: 3.240

10.  Expression analysis in multiple muscle groups and serum reveals complexity in the microRNA transcriptome of the mdx mouse with implications for therapy.

Authors:  Thomas C Roberts; K Emelie M Blomberg; Graham McClorey; Samir El Andaloussi; Caroline Godfrey; Corinne Betts; Thibault Coursindel; Michael J Gait; C I Edvard Smith; Matthew J A Wood
Journal:  Mol Ther Nucleic Acids       Date:  2012-08-14       Impact factor: 10.183

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