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Characterisation of connexin expression and electrophysiological properties in stable clones of the HL-1 myocyte cell line.

Authors :
Dias P
Desplantez T
El-Harasis MA
Chowdhury RA
Ullrich ND
Cabestrero de Diego A
Peters NS
Severs NJ
MacLeod KT
Dupont E
Source :
PloS one [PLoS One] 2014 Feb 28; Vol. 9 (2), pp. e90266. Date of Electronic Publication: 2014 Feb 28 (Print Publication: 2014).
Publication Year :
2014

Abstract

The HL-1 atrial line contains cells blocked at various developmental stages. To obtain homogeneous sub-clones and correlate changes in gene expression with functional alterations, individual clones were obtained and characterised for parameters involved in conduction and excitation-contraction coupling. Northern blots for mRNAs coding for connexins 40, 43 and 45 and calcium handling proteins (sodium/calcium exchanger, L- and T-type calcium channels, ryanodine receptor 2 and sarco-endoplasmic reticulum calcium ATPase 2) were performed. Connexin expression was further characterised by western blots and immunofluorescence. Inward currents were characterised by voltage clamp and conduction velocities measured using microelectrode arrays. The HL-1 clones had similar sodium and calcium inward currents with the exception of clone 2 which had a significantly smaller calcium current density. All the clones displayed homogenous propagation of electrical activity across the monolayer correlating with the levels of connexin expression. Conduction velocities were also more sensitive to inhibition of junctional coupling by carbenoxolone (∼ 80%) compared to inhibition of the sodium current by lidocaine (∼ 20%). Electrical coupling by gap junctions was the major determinant of conduction velocities in HL-1 cell lines. In summary we have isolated homogenous and stable HL-1 clones that display characteristics distinct from the heterogeneous properties of the original cell line.

Details

Language :
English
ISSN :
1932-6203
Volume :
9
Issue :
2
Database :
MEDLINE
Journal :
PloS one
Publication Type :
Academic Journal
Accession number :
24587307
Full Text :
https://doi.org/10.1371/journal.pone.0090266