Development of the cardiac conduction system and the possible relation to predilection sites of arrhythmogenesis

被引:33
作者
Jongbloed, M. R. M. [1 ,2 ]
Mahtab, E. A. F. [1 ]
Blom, N. A. [3 ]
Schalij, M. J. [2 ]
Groot, A. C. Gittenberger-de [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Anat & Embryol, Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Cardiol, Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Paediat Cardiol, Leiden, Netherlands
来源
THESCIENTIFICWORLDJOURNAL | 2008年 / 8卷
关键词
cardiac conduction system development; arrhythmias; electrophysiology; pulmonary veins; cardiac development;
D O I
10.1100/tsw.2008.40
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The cardiac conduction system (CCS) encompasses a complex system responsible for the coordinated contraction of the heart. In the developing heart, as well as in the adult heart, tissues of the (putative) CCS are characterized by different properties than the surrounding working myocardium, which can be observed on a histological level, as well as by the expression patterns of several immunohistological and molecular markers. In recent years, many markers have been studied that have helped to elucidate the processes involved in CCS development. It has become clear that multiple genes, cells and their interactions are involved in this complex process. In this article, an overview of the current knowledge of CCS development is supplied. Furthermore, several controversies regarding conduction system development are discussed, as well as the possible significance of embryologic development of the CCS for the development of arrhythmias later in life.
引用
收藏
页码:239 / 269
页数:31
相关论文
共 205 条
[91]   The transcriptional repressor Tbx3 delineates the developing central conduction system of the heart [J].
Hoogaars, WMH ;
Tessari, A ;
Moorman, AFM ;
de Boer, PAJ ;
Hagoort, J ;
Soufan, AT ;
Campione, M ;
Christoffels, VM .
CARDIOVASCULAR RESEARCH, 2004, 62 (03) :489-499
[92]   Induction of Purkinje fiber differentiation by coronary arterialization [J].
Hyer, J ;
Johansen, M ;
Prasad, A ;
Wessels, A ;
Kirby, ML ;
Gourdie, RG ;
Mikawa, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) :13214-13218
[93]   Homeobox protein Hop functions in the adult cardiac conduction system [J].
Ismat, FA ;
Zhang, MZ ;
Kook, H ;
Huang, B ;
Zhou, R ;
Ferrari, VA ;
Epstein, JA ;
Patel, VV .
CIRCULATION RESEARCH, 2005, 96 (08) :898-903
[94]   Distinctive electrophysiological properties of pulmonary veins in patients with atrial fibrillation [J].
Jaïs, P ;
Hocini, M ;
Macle, L ;
Choi, KJ ;
Deisenhofer, I ;
Weerasooriya, R ;
Shah, DC ;
Garrigue, S ;
Raybaud, F ;
Scavee, C ;
Le Metayer, P ;
Clémenty, J ;
Haïssaguerre, M .
CIRCULATION, 2002, 106 (19) :2479-2485
[96]   The internodal pathways of the human heart [J].
James, TN .
PROGRESS IN CARDIOVASCULAR DISEASES, 2001, 43 (06) :495-535
[97]   Absence of Msx2 does not affect cardiac conduction or rescue conduction defects associated with Nkx2-5 mutation [J].
Jay, PY ;
Maguire, CT ;
Wakimoto, H ;
Izumo, S ;
Berul, CI .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2005, 16 (01) :82-85
[98]   Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system [J].
Jay, PY ;
Harris, BS ;
Maguire, CT ;
Buerger, A ;
Wakimoto, H ;
Tanaka, M ;
Kupershmidt, S ;
Roden, DM ;
Schultheiss, TM ;
O'Brien, TX ;
Gourdie, RG ;
Berul, CI ;
Izumo, S .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (08) :1130-1137
[99]   Patterns of gene expression associated with BMP-2-induced osteoblast and adipocyte differentiation of mesenchymal progenitor cell 3T3-F442A [J].
Ji, XH ;
Chen, D ;
Xu, C ;
Harris, SE ;
Mundy, GR ;
Yoneda, T .
JOURNAL OF BONE AND MINERAL METABOLISM, 2000, 18 (03) :132-139
[100]   Development of the right ventricular inflow tract and moderator band - A possible morphological and functional explanation for Mahaim tachycardia [J].
Jongbloed, MRM ;
Wijffels, MCEF ;
Schalij, MJ ;
Blom, NA ;
Poelmann, RE ;
van der Laarse, A ;
Mentink, MMT ;
Wang, Z ;
Fishman, GI ;
Gittenberger-de Groot, AC .
CIRCULATION RESEARCH, 2005, 96 (07) :776-783