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心脏传导系统的分子谱分析:新时代的曙光。

Molecular Profiling of the Cardiac Conduction System: the Dawn of a New Era.

机构信息

Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.

Division of Pediatric Cardiology, Department of Pediatrics, Stanford University, Stanford, CA, 94305, USA.

出版信息

Curr Cardiol Rep. 2021 Jul 1;23(8):103. doi: 10.1007/s11886-021-01536-w.

DOI:10.1007/s11886-021-01536-w
PMID:34196831
Abstract

PURPOSE OF REVIEW

Recent technological advances have led to an increased ability to define the gene expression profile of the cardiac conduction system (CCS). Here, we review the most salient studies to emerge in recent years and discuss existing gaps in our knowledge as well as future areas of investigation.

RECENT FINDINGS

Molecular profiling of the CCS spans several decades. However, the advent of high-throughput sequencing strategies has allowed for the discovery of unique transcriptional programs of the many diverse CCS cell types. The CCS, a diverse structure with significant inter- and intra-component cellular heterogeneity, is essential to the normal function of the heart. Progress in transcriptomic profiling has improved the resolution and depth of characterization of these unique and clinically relevant CCS cell types. Future studies leveraging this big data will play a crucial role in improving our understanding of CCS development and function as well as translating these findings into tangible translational tools for the improved detection, prevention, and treatment of cardiac arrhythmias.

摘要

目的综述

近年来,技术的进步使得人们能够更精确地定义心脏传导系统(CCS)的基因表达谱。在此,我们对近年来出现的最相关研究进行综述,并讨论我们现有知识的空白以及未来的研究领域。

最近的发现

对 CCS 的分子谱分析已经有几十年的历史了。然而,高通量测序策略的出现使得人们能够发现许多不同的 CCS 细胞类型独特的转录程序。CCS 是一个具有显著的细胞间和细胞内异质性的多样化结构,对心脏的正常功能至关重要。转录组谱分析的进展提高了对这些独特的、具有临床相关性的 CCS 细胞类型的特征描述的分辨率和深度。未来利用这些大数据的研究将在提高我们对 CCS 发育和功能的理解以及将这些发现转化为可用于提高心脏心律失常检测、预防和治疗的切实可行的转化工具方面发挥关键作用。

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本文引用的文献

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Nat Methods. 2021 Jan;18(1):9-14. doi: 10.1038/s41592-020-01033-y.
2
Anatomy of the cardiac conduction system.心脏传导系统解剖。
Pacing Clin Electrophysiol. 2021 Jan;44(1):15-25. doi: 10.1111/pace.14107. Epub 2020 Nov 12.
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ATAC-Seq Reveals an Enhancer That Regulates Sinoatrial Node Development and Function.ATAC-Seq 揭示了一个调节窦房结发育和功能的增强子。
J Cardiovasc Dev Dis. 2022 Nov 18;9(11):402. doi: 10.3390/jcdd9110402.
Circ Res. 2020 Dec 4;127(12):1502-1518. doi: 10.1161/CIRCRESAHA.120.317145. Epub 2020 Oct 12.
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Genome-Wide Analysis Identifies an Essential Human TBX3 Pacemaker Enhancer.全基因组分析鉴定出人类 TBX3 起搏器的必需增强子。
Circ Res. 2020 Dec 4;127(12):1522-1535. doi: 10.1161/CIRCRESAHA.120.317054. Epub 2020 Oct 12.
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T-box transcription factor 3 governs a transcriptional program for the function of the mouse atrioventricular conduction system.T 盒转录因子 3 调控着小鼠房室传导系统功能的转录程序。
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Heterogeneity in mRNA Translation.mRNA 翻译的异质性。
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Transcriptional and Cellular Diversity of the Human Heart.人类心脏的转录和细胞多样性。
Circulation. 2020 Aug 4;142(5):466-482. doi: 10.1161/CIRCULATIONAHA.119.045401. Epub 2020 May 14.
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Variable Arrangement of the Atrioventricular Conduction Axis Within the Triangle of Koch: Implications for Permanent His Bundle Pacing.房室传导轴在 Koch 三角内的可变排列:对永久性希氏束起搏的影响。
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