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兔房室传导轴上离子通道转录本的表达

Ion channel transcript expression at the rabbit atrioventricular conduction axis.

作者信息

Greener Ian D, Tellez James O, Dobrzynski Halina, Yamamoto Mitsuru, Graham Gillian M, Billeter Rudi, Boyett Mark R

机构信息

Faculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.

出版信息

Circ Arrhythm Electrophysiol. 2009 Jun;2(3):305-15. doi: 10.1161/CIRCEP.108.803569. Epub 2009 Apr 2.

Abstract

BACKGROUND

Little is known about the distribution of gap junctions and ion channels in the atrioventricular node, even though the physiology and pathology of the atrioventricular node is ultimately dependent on them.

METHODS AND RESULTS

The abundance of 30 transcripts for markers, gap junctions, ion channels, and Ca(2+)-handling proteins in different regions of the rabbit atrioventricular node (nodal extension and proximal and distal penetrating bundle of His as well as atrial and ventricular muscle) was measured using a novel quantitative polymerase chain reaction technique and in situ hybridization. The expression profile of the nodal extension (slow pathway into penetrating bundle) was similar to that of the sinoatrial node. For example, in the nodal extension, in contrast to the atrial muscle and as expected for a slowly conducting tissue with pacemaker activity, there was no or reduced expression of Cx43, Na(v)1.5, Ca(v)1.2, K(v)1.4, KChIP2, and RYR3 and high expression of Ca(v)1.3 and HCN4. The expression profile of the penetrating bundle was less specialized. In situ hybridization revealed a transitional zone with reduced expression of Cx43, Na(v)1.5, and KChIP2 that may form the fast pathway into the penetrating bundle.

CONCLUSIONS

At the atrioventricular node, the expression of gap junctions and ion channels in the nodal extension (slow pathway) and a transitional zone (putative fast pathway) as well as the penetrating bundle (output pathway) is specialized and heterogeneous and roughly matches the electrophysiology of the different regions.

摘要

背景

尽管房室结的生理学和病理学最终依赖于缝隙连接和离子通道,但关于它们在房室结中的分布情况却知之甚少。

方法与结果

使用一种新型定量聚合酶链反应技术和原位杂交法,测量了兔房室结不同区域(结延伸部、希氏束近端和远端穿入束以及心房和心室肌)中30种标记物、缝隙连接、离子通道和钙处理蛋白的转录本丰度。结延伸部(进入穿入束的慢径路)的表达谱与窦房结相似。例如,在结延伸部,与心房肌不同,且正如具有起搏活动的缓慢传导组织所预期的那样,Cx43、Na(v)1.5、Ca(v)1.2、K(v)1.4、KChIP2和RYR3的表达无或降低,而Ca(v)1.3和HCN4的表达较高。穿入束的表达谱不太特异。原位杂交显示一个Cx43、Na(v)1.5和KChIP2表达降低的过渡区,该区域可能形成进入穿入束的快径路。

结论

在房室结,结延伸部(慢径路)、过渡区(假定的快径路)以及穿入束(输出径路)中缝隙连接和离子通道的表达具有特异性且不均一,大致与不同区域的电生理情况相符。

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