Expression of the hyperpolarization-activated cyclic nucleotide-gated cation channel HCN4 during mouse heart development

被引:90
作者
Garcia-Frigola, C
Shi, YQ
Evans, SM [1 ]
机构
[1] Univ Calif San Diego, Inst Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
关键词
hyperpolarization-activated cyclic nucleotide-gated cation channels; sinus venosus; development; pacemaker;
D O I
10.1016/S1567-133X(03)00125-X
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
HCN4 is a hyperpolarization-activated nucleotide-gated cation channel involved in the generation of the I-f current that drives cardiac pacemaker activity. Previous studies have demonstrated that HCN4 is highly expressed in a restricted manner in adult sinoatrial (SA) node [Eur. J. Biochem. 268 (2001) 1646]. However, its developmental expression pattern is unknown. We have examined expression of HCN4 mRNA during mouse heart development. HCN4 mRNA was first detected in the cardiac crescent at embryonic day (ED) 7.5. At ED 8 it was symmetrically located in the most caudal portion of the heart tube, the sinus venosus where pacemaker activity has previously been reported [Am. J. Physiol. 212 (1967) 407]. With further development, HCN4 expression became asymmetrically distributed, occupying the dorsal wall of the right atria, and was progressively restricted to the junction of the right atrial appendage and the superior vena cava. The site of HCN4 expression in late embryonic heart coincided with the location of the SA node in postnatal and adult heart [Cardiovasc. Res. 52 (2001) 51]. Our results suggest that HCN4 may be a unique marker of the developing SA node. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:777 / 783
页数:7
相关论文
共 12 条
[1]   From funny current to HCN channels: 20 years of excitation [J].
Accili, EA ;
Proenza, C ;
Baruscotti, M ;
DiFrancesco, D .
NEWS IN PHYSIOLOGICAL SCIENCES, 2002, 17 :32-37
[2]   Normal development of the pulmonary veins in human embryos and formulation at a morphogenetic concept for sinus venosus defects [J].
Blom, NA ;
Gittenberger-de Groot, AC ;
Jongeneel, TH ;
DeRuiter, MC ;
Poelmann, RE ;
Ottenkamp, J .
AMERICAN JOURNAL OF CARDIOLOGY, 2001, 87 (03) :305-309
[3]   THE PACEMAKER CURRENT (I-F) PLAYS AN IMPORTANT ROLE IN REGULATING SA NODE PACEMAKER ACTIVITY [J].
DIFRANCESCO, D .
CARDIOVASCULAR RESEARCH, 1995, 30 (02) :307-308
[4]  
DIFRANCESCO D, 1993, ANNU REV PHYSIOL, V58, P299
[5]   Characteristics of hyperpolarization-activated cation currents in portal vein smooth muscle cells [J].
Greenwood, IA ;
Prestwich, SA .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 282 (04) :C744-C753
[6]   A family of hyperpolarization-activated mammalian cation channels [J].
Ludwig, A ;
Zong, XG ;
Jeglitsch, M ;
Hofmann, F ;
Biel, M .
NATURE, 1998, 393 (6685) :587-591
[7]   Properties of the hyperpolarization-activated current (If) in isolated mouse sino-atrial cells [J].
Mangoni, ME ;
Nargeot, J .
CARDIOVASCULAR RESEARCH, 2001, 52 (01) :51-64
[8]   Cellular expression and functional characterization of four hyperpolarization-activated pacemaker channels in cardiac and neuronal tissues [J].
Moosmang, S ;
Stieber, J ;
Zong, XG ;
Biel, M ;
Hofmann, F ;
Ludwig, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (06) :1646-1652
[9]   Identification of a gene encoding a hyperpolarization-activated pacemaker channel of brain [J].
Santoro, B ;
Liu, DT ;
Yao, H ;
Bartsch, D ;
Kandel, ER ;
Siegelbaum, SA ;
Tibbs, GR .
CELL, 1998, 93 (05) :717-729
[10]   Molecular and functional heterogeneity of hyperpolarization-activated pacemaker channels in the mouse CNS [J].
Santoro, B ;
Chen, S ;
Lüthi, A ;
Pavlidis, P ;
Shumyatsky, GP ;
Tibbs, GR ;
Siegelbaum, SA .
JOURNAL OF NEUROSCIENCE, 2000, 20 (14) :5264-5275