Validation of formamide as a detubulation agent in isolated rat cardiac cells.

Kawai M, Hussain M, and Orchard CH. Am J Heart Circ Physiol 277: H603-H609, 1999 developed a technique to detubulate rat ventricular myocytes using formamide and showed that detubulation results in a decrease in cell capacitance, Ca(2+) current density, and Ca(2+) transient amplitude. We have investigated the mechanism of this detubulation and possible direct effects of formamide. Staining ventricular cells with di-8-ANEPPS showed that the t tubule membranes remain inside the cell after detubulation; trapping of FITC-labeled dextran within the t tubules showed that detubulation occurs during formamide washout and that the t tubules appear to reseal within the cell. Detubulation had no effect on the microtubule network but resulted in loss of synchronous Ca(2+) release on electrical stimulation. In contrast, formamide treatment of atrial cells did not significantly change cell capacitance, Ca(2+) current amplitude, action potential configuration, the Ca(2+) transient or the response of the Ca(2+) transient to isoprenaline. We conclude that formamide washout induces detubulation of single rat ventricular myocytes, leaving the t tubules within the cell, but without direct effects on cell proteins that might alter cell function.

[1]  P. Bennett Anchors Aweigh!: ion channels, cytoskeletal proteins, and cellular excitability. , 2000, Circulation research.

[2]  Katherine A. Sheehan,et al.  Activation and propagation of Ca(2+) release during excitation-contraction coupling in atrial myocytes. , 2001, Biophysical journal.

[3]  W. Giles,et al.  Location of the initiation site of calcium transients and sparks in rabbit heart Purkinje cells , 2001, The Journal of physiology.

[4]  M. Boyett,et al.  Effect of the microtubule polymerizing agent taxol on contraction, Ca2+ transient and L‐type Ca2+ current in rat ventricular myocytes , 1999, The Journal of physiology.

[5]  E. White,et al.  Cardiac microtubules are more resistant to chemical depolymerisation in streptozotocin-induced diabetes in the rat , 2002, Pflügers Archiv.

[6]  R. Fischmeister,et al.  Longitudinal distribution of Na+ and Ca2+ channels and β‐adrenoceptors on the sarcolemmal membrane of frog cardiomyocytes , 1997, The Journal of physiology.

[7]  G. Christé Localization of K(+) channels in the tubules of cardiomyocytes as suggested by the parallel decay of membrane capacitance, IK(1) and IK(ATP) during culture and by delayed IK(1) response to barium. , 1999, Journal of molecular and cellular cardiology.

[8]  N. Shepherd,et al.  Ionic diffusion in transverse tubules of cardiac ventricular myocytes. , 1998, American journal of physiology. Heart and circulatory physiology.

[9]  C W Balke,et al.  Local Ca2+ transients (Ca2+ sparks) originate at transverse tubules in rat heart cells. , 1995, The Journal of physiology.

[10]  P. Lipp,et al.  Spatially non‐uniform Ca2+ signals induced by the reduction of transverse tubules in citrate‐loaded guinea‐pig ventricular myocytes in culture. , 1996, The Journal of physiology.

[11]  Y. Furuya,et al.  Ultra‐high‐resolution scanning electron microscopy of the sarcoplasmic reticulum of the rat atrial myocardial cells , 1997, The Anatomical record.

[12]  A. Caswell,et al.  Immunolocalization of sarcolemmal dihydropyridine receptor and sarcoplasmic reticular triadin and ryanodine receptor in rabbit ventricle and atrium , 1995, The Journal of cell biology.

[13]  E Page,et al.  Quantitative ultrastructural analysis in cardiac membrane physiology. , 1978, The American journal of physiology.

[14]  M. Stromer The cytoskeleton in skeletal, cardiac and smooth muscle cells. , 1998, Histology and histopathology.

[15]  M. Forbes,et al.  Membrane systems of guinea pig myocardium: Ultrastructure and morphometric studies , 1988, The Anatomical Record.

[16]  R. Haugland Handbook of fluorescent probes and research products , 2002 .

[17]  Susan C. Brown,et al.  Accessibility of T-tubule vacuoles to extracellular dextran and DNA: mechanism and potential application of vacuolation , 1998, Journal of Muscle Research & Cell Motility.

[18]  P. Dan,et al.  Distribution of proteins implicated in excitation-contraction coupling in rat ventricular myocytes. , 2000, Biophysical journal.

[19]  L. Blatter,et al.  Calcium gradients during excitation‐contraction coupling in cat atrial myocytes. , 1996, The Journal of physiology.

[20]  Y. Hirota,et al.  Formation of planar and spiral Ca2+ waves in isolated cardiac myocytes. , 1999, Biophysical journal.

[21]  M. Kawai,et al.  Excitation-contraction coupling in rat ventricular myocytes after formamide-induced detubulation. , 1999, American journal of physiology. Heart and circulatory physiology.