Evidence map›Paper›PMID 24587307›Full record

ArticlePloS one2014

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

Priyanthi Dias, Thomas Desplantez, Majd A El-Harasis, Rasheda A Chowdhury, Nina D Ullrich, Alberto Cabestrero de Diego, Nicholas S Peters, Nicholas J Severs, Kenneth T MacLeod, Emmanuel Dupont

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 46 citations in OpenAlex.

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  10. MulticellularFrontiers in cardiovascular medicine · 2020
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  18. Article
  19. Review
  20. Biology of the cardiac myocyte in heart disease.Molecular biology of the cell · 2016
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Priyanthi DiasMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Thomas DesplantezMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Majd A El-HarasisMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Rasheda A ChowdhuryMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Nina D UllrichMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Alberto Cabestrero de DiegoMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Nicholas S PetersMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Nicholas J SeversMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Kenneth T MacLeodMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Emmanuel DupontMyocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Imperial College London · GB

Funding

British Heart Foundation PG/05/111British Heart Foundation PG/09/012/26846British Heart Foundation RG/10/11/28457
6 · The paper itself

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.

Indexed as

Action PotentialsAnimalsCalcium Channels, L-TypeCalcium Channels, T-TypeCell LineClone CellsConnexin 43ConnexinsExcitation Contraction CouplingGap Junction alpha-5 ProteinGap JunctionsGene ExpressionHeart AtriaHeart Conduction SystemHumansMiceCalcium Channels, L-TypeCalcium Channels, T-TypeConnexin 43connexin 45ConnexinsGap Junction alpha-5 ProteinGJA1 protein, mouseRyanodine Receptor Calcium Release ChannelSarcoplasmic Reticulum Calcium-Transporting ATPasesSodium-Calcium Exchanger

Identifiers

PMID24587307
PMCPMC3938655
OpenAlexW2003397375

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.