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Connexin43 ablation in foetal atrial myocytes decreases electrical coupling, partner connexins, and sodium current

Desplantez, Thomas ; McCain, Megan L. ; Beauchamp, Philippe ; Rigoli, Ghislaine ; Rothen-Rutishauser, Barbara ; Parker, Kevin Kit ; Kleber, Andre G.

In: Cardiovascular Research, 2012, vol. 94, no. 1, p. 58-65

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    Titel
    • Connexin43 ablation in foetal atrial myocytes decreases electrical coupling, partner connexins, and sodium current
    Autor
    • Desplantez, Thomas. Department of Physiology, University of Bern, Bern, Switzerland
    • McCain, Megan L.. Disease Biophysics Group, School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
    • Beauchamp, Philippe. Department of Physiology, University of Bern, Bern, Switzerland
    • Rigoli, Ghislaine. Department of Physiology, University of Bern, Bern, Switzerland
    • Rothen-Rutishauser, Barbara. Department of Anatomy, University of Bern, Bern, Switzerland
    • Parker, Kevin Kit. Disease Biophysics Group, School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
    • Kleber, Andre G.. Department of Physiology, University of Bern, Bern, Switzerland
    Dokumententyp
    • Postprint
    Sprache
    • Englisch
    Veröffentlicht in
    • Cardiovascular Research, 2012, vol. 94, no. 1, p. 58-65. Oxford University Press
    Andere elektronische Ausgabe
    OAI-PMH-ID
    • oai:doc.rero.ch:290809
    Summary
    Aims Remodelling and regional gradients in expression of connexins (Cx) are thought to contribute to atrial electrical dysfunction and atrial fibrillation. We assessed the effect of interaction between Cx43, Cx40, and Cx45 on atrial cell-to-cell coupling and inward Na current (INa) in engineered pairs of atrial myocytes derived from wild-type mice (Cx43+/+) and mice with genetic ablation of Cx43 (Cx43−/−). Methods and results Cell pairs were engineered by microcontact printing from atrial Cx43+/+ and Cx43−/− murine myocytes (1 day before birth, 3-5 days in culture). Dual and single voltage clamp were used to measure intercellular electrical conductance, gj, and its dependence on transjunctional voltage, Vj, single gap junction channel conductances, and INa. 3D reconstructions of Cx43, Cx40, and Cx45 immunosignals in gap junctions were made from confocal slices. Full genetic Cx43 ablation produced a decrease in immunosignals of Cx40 to 62 ± 10% (mean ± SE; n= 17) and Cx45 to 66 ± 8% (n= 16). Gj decreased from 80 ± 9 nS (Cx43+/+, n= 17) to 24 ± 2 nS (Cx43−/−, n= 35). Single channel analysis showed a shift in the main peak of the channel histogram from 49 ± 1.7 nS (Cx43+/+) to 67 ± 1.8 nS (Cx43−/−) with a second minor peak appearing at 27 ± 1.5 pS. The dependence of gj on Vj decreased with Cx43 ablation. Importantly, peak INa decreased from −350 ± 44 pA/pF (Cx43+/+) to −154 ± 28 pA/pF (Cx43−/−). Conclusions The dependence of Cx40, Cx45, and INa on Cx43 expression indicates a complex interaction between connexins and INa in the atrial intercalated discs that is likely to be of relevance for arrhythmogenesis