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July 21, 2006Circulation Research244 citations

Cardiac Sodium Channel Na v 1.5 Is Regulated by a Multiprotein Complex Composed of Syntrophins and Dystrophin

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BGBruno GavilletJRJean‐Sébastien RougierADAndrea A. Domenighetti

Key Result

Dystrophin deficiency in mdx(5cv) mice caused a 50% decrease in Na(v)1.5 protein levels, a 29% decrease in sodium current, and an 18% increase in QRS duration compared with controls.

Key Points

  • This study aims to understand how the PDZ domain-binding motif of Na(v)1.5 influences its interaction with dystrophin and syntrophins.
  • Used pull-down experiments with Na(v)1.5 C-terminus fusion proteins and protein extracts from human or mouse hearts.
  • Performed western blot analyses on dystrophin-deficient mdx(5cv) mice to assess Na(v)1.5 protein levels.
  • Conducted patch-clamp experiments on isolated mdx(5cv) cardiomyocytes to evaluate sodium current changes.
  • Na(v)1.5 protein levels were decreased by 50% in mdx(5cv) hearts with no change in mRNA levels.
  • Sodium current in mdx(5cv) cardiomyocytes decreased by 29%.
  • ECG measurements showed a 19% reduction in P wave amplitude and an 18% increase in QRS complex duration compared to controls.

Structured PICO

P
Population
Human or mouse heart protein extracts, dystrophin-deficient mdx(5cv) mice, and isolated mdx(5cv) cardiomyocytes
E
Exposure
Dystrophin deficiency (mdx(5cv) model) and truncation of the PDZ domain-binding motif
C
Comparator
Wild-type/control mice and intact PDZ domain-binding motif
O
Outcome
Na(v)1.5 protein levels, sodium current, and ECG parameters (P wave amplitude, QRS duration)surrogate

The dystrophin protein complex is required for proper expression and function of the cardiac sodium channel Na(v)1.5, providing a mechanistic explanation for conduction abnormalities in dystrophinopathies.

Abstract

The cardiac sodium channel Na(v)1.5 plays a key role in cardiac excitability and conduction. The purpose of this study was to elucidate the role of the PDZ domain-binding motif formed by the last three residues (Ser-Ile-Val) of the Na(v)1.5 C-terminus. Pull-down experiments were performed using Na(v)1.5 C-terminus fusion proteins and human or mouse heart protein extracts, combined with mass spectrometry analysis. These experiments revealed that the C-terminus associates with dystrophin, and that this interaction was mediated by alpha- and beta-syntrophin proteins. Truncation of the PDZ domain-binding motif abolished the interaction. We used dystrophin-deficient mdx(5cv) mice to study the role of this protein complex in Na(v)1.5 function. Western blot experiments revealed a 50% decrease in the Na(v)1.5 protein levels in mdx(5cv) hearts, whereas Na(v)1.5 mRNA levels were unchanged. Patch-clamp experiments showed a 29% decrease of sodium current in isolated mdx(5cv) cardiomyocytes. Finally, ECG measurements of the mdx(5cv) mice exhibited a 19% reduction in the P wave amplitude, and an 18% increase of the QRS complex duration, compared with controls. These results indicate that the dystrophin protein complex is required for the proper expression and function of Na(v)1.5. In the absence of dystrophin, decreased sodium current may explain the alterations in cardiac conduction observed in patients with dystrophinopathies.

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Cite This Study

Gavillet et al. (2006) studied Dystrophin deficiency. Dystrophin deficiency vs. Controls was evaluated on Na(v)1.5 protein levels and sodium current. Dystrophin deficiency in mdx(5cv) mice caused a 50% decrease in Na(v)1.5 protein levels, a 29% decrease in sodium current, and an 18% increase in QRS duration compared with controls.

synapsesocial.com/papers/6a63a502a23d78a77db6cfc4https://doi.org/10.1161/01.res.0000237466.13252.5e
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