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HL-1心肌细胞系稳定克隆中连接蛋白表达及电生理特性的表征

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

作者信息

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

机构信息

Myocardial Function Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.

出版信息

PLoS One. 2014 Feb 28;9(2):e90266. doi: 10.1371/journal.pone.0090266. eCollection 2014.

DOI:10.1371/journal.pone.0090266
PMID:24587307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3938655/
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.

摘要

HL-1心房细胞系包含处于不同发育阶段受阻的细胞。为了获得同质亚克隆,并将基因表达的变化与功能改变相关联,我们分离了单个克隆,并对参与传导和兴奋-收缩偶联的参数进行了表征。对编码连接蛋白40、43和45以及钙处理蛋白(钠/钙交换体、L型和T型钙通道、雷诺丁受体2和肌浆网钙ATP酶2)的mRNA进行了Northern印迹分析。通过蛋白质印迹和免疫荧光进一步表征连接蛋白的表达。通过电压钳表征内向电流,并使用微电极阵列测量传导速度。除克隆2的钙电流密度明显较小外,HL-1克隆具有相似的钠和钙内向电流。所有克隆在单层上均表现出电活动的均匀传播,这与连接蛋白的表达水平相关。与利多卡因对钠电流的抑制作用(约20%)相比,HL-1细胞系的传导速度对羧苄青霉素对连接偶联的抑制作用(约80%)更敏感。间隙连接介导的电偶联是HL-1细胞系传导速度的主要决定因素。总之,我们分离出了同质且稳定的HL-1克隆,它们表现出与原始细胞系的异质性不同的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/6524739f4ea4/pone.0090266.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/b1f08e50a07e/pone.0090266.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/952146fe7145/pone.0090266.g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/6492158b11da/pone.0090266.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/7b728fb0e030/pone.0090266.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/102cd83f5582/pone.0090266.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/4b0e3f1e4ee5/pone.0090266.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/6524739f4ea4/pone.0090266.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/b1f08e50a07e/pone.0090266.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/952146fe7145/pone.0090266.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/695813c9689d/pone.0090266.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/95e9acbe436d/pone.0090266.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/15dd78037b06/pone.0090266.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/6492158b11da/pone.0090266.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/7b728fb0e030/pone.0090266.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/102cd83f5582/pone.0090266.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/4b0e3f1e4ee5/pone.0090266.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/3938655/6524739f4ea4/pone.0090266.g010.jpg

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