Caveolae in Ventricular Myocytes Are Required for Stretch-Dependent Conduction Slowing

J Mol Cell Cardiol. 2014 Nov;76:265-74. doi: 10.1016/j.yjmcc.2014.09.014. Epub 2014 Sep 26.

Abstract

Mechanical stretch of cardiac muscle modulates action potential propagation velocity, causing potentially arrhythmogenic conduction slowing. The mechanisms by which stretch alters cardiac conduction remain unknown, but previous studies suggest that stretch can affect the conformation of caveolae in myocytes and other cell types. We tested the hypothesis that slowing of action potential conduction due to cardiac myocyte stretch is dependent on caveolae. Cardiac action potential propagation velocities, measured by optical mapping in isolated mouse hearts and in micropatterned mouse cardiomyocyte cultures, decreased reversibly with volume loading or stretch, respectively (by 19±5% and 26±4%). Stretch-dependent conduction slowing was not altered by stretch-activated channel blockade with gadolinium or by GsMTx-4 peptide, but was inhibited when caveolae were disrupted via genetic deletion of caveolin-3 (Cav3 KO) or membrane cholesterol depletion by methyl-β-cyclodextrin. In wild-type mouse hearts, stretch coincided with recruitment of caveolae to the sarcolemma, as observed by electron microscopy. In myocytes from wild-type but not Cav3 KO mice, stretch significantly increased cell membrane capacitance (by 98±64%), electrical time constant (by 285±149%), and lipid recruitment to the bilayer (by 84±39%). Recruitment of caveolae to the sarcolemma during physiologic cardiomyocyte stretch slows ventricular action potential propagation by increasing cell membrane capacitance.

Keywords: Capacitance; Cardiac mechanoelectric feedback; Caveolae.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Action Potentials
  • Animals
  • Caveolae / physiology*
  • Caveolin 3 / genetics
  • Caveolin 3 / metabolism
  • Cells, Cultured
  • Heart Conduction System*
  • Heart Ventricles / cytology
  • Mechanotransduction, Cellular
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myocytes, Cardiac / physiology*
  • Myocytes, Cardiac / ultrastructure
  • Patch-Clamp Techniques
  • Sarcolemma / metabolism
  • Ventricular Function
  • Ventricular Pressure

Substances

  • Cav3 protein, mouse
  • Caveolin 3