Literature DB >> 1279981

Differences in gap junction channels between cardiac myocytes, fibroblasts, and heterologous pairs.

M B Rook1, A C van Ginneken, B de Jonge, A el Aoumari, D Gros, H J Jongsma.   

Abstract

Cultures of neonatal rat heart cells contain predominantly myocytes and fibroblastic cells. Most abundant are groups of synchronously contracting myocytes, which are electrically well coupled through large gap junctions. Cardiac fibroblasts may be electrically coupled to each other and to adjacent myocytes, be it with low intercellular conductances. Nevertheless, synchronously beating myocytes interconnected via a fibroblast were present, demonstrating that nonexcitable cardiac cells are capable of passive impulse conduction. In fibroblast pairs as well as in myocyte-fibroblast cell pairs, no sensitivity to junctional voltage could be detected when transjunctional conductance was > 1-2 nS. However, in pairs coupled by a conductance of < 1 nS, complex voltage-dependent gating was evident; gap junction channel open probability decreased with increasing junctional voltage but a nongated residual conductance remained at all voltages tested. Single gap junction channel conductance between fibroblasts was approximately 21 pS, very similar to an approximately 18-pS channel conductance that was found between myocytes next to the major conductance of 43 pS. Single-channel conductance in heterologous myocyte-fibroblast gap junctions was approximately 32 pS, which matches the theoretical value of 29 pS for gap junction channels composed of a fibroblast connexon and the major myocyte connexon. A site-directed antibody against rat heart gap junction protein connexin43 recognized gap junctions between neonatal cardiomyocytes, as demonstrated by immunocytochemical labeling. In contrast, junctions between fibroblasts showed no labeling, while in myocyte-fibroblast junctions labeling occasionally was present. Our results suggest the existence of two gap junction proteins between neonatal rat cardiocytes, connexin43 and another yet unidentified connexin. An alternative explanation (cell-specific regulation of the conductance of connexin43 channels) is discussed.

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Year:  1992        PMID: 1279981     DOI: 10.1152/ajpcell.1992.263.5.C959

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  86 in total

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3.  K+ currents activated by depolarization in cardiac fibroblasts.

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5.  The relevance of non-excitable cells for cardiac pacemaker function.

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6.  Loading effect of fibroblast-myocyte coupling on resting potential, impulse propagation, and repolarization: insights from a microstructure model.

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7.  Cardiac alternans induced by fibroblast-myocyte coupling: mechanistic insights from computational models.

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8.  Modulation of conduction velocity by nonmyocytes in the low coupling regime.

Authors:  Vincent Jacquemet; Craig S Henriquez
Journal:  IEEE Trans Biomed Eng       Date:  2009-03       Impact factor: 4.538

Review 9.  Cardiac fibroblasts : Active players in (atrial) electrophysiology?

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Journal:  Herzschrittmacherther Elektrophysiol       Date:  2018-02-01

10.  Mechanically induced potentials in atrial fibroblasts from rat hearts are sensitive to hypoxia/reoxygenation.

Authors:  Andre Kamkin; Irina Kiseleva; Kay-Dietrich Wagner; Ilja Lozinsky; Joachim Günther; Holger Scholz
Journal:  Pflugers Arch       Date:  2003-03-08       Impact factor: 3.657

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