Transcription factors Csx/Nkx2.5 and GATA4 distinctly regulate expression of Ca2+ channels in neonatal rat heart

被引:39
|
作者
Wang, Yan
Morishima, Masaki
Zheng, Mingqi
Uchino, Tomoko
Mannen, Kazuaki
Takahashi, Akira
Nakaya, Yutaka
Komuro, Issei
Ono, Katsushige [1 ]
机构
[1] Oita Univ, Sch Med, Dept Cardiovasc Sci, Oita 8795593, Japan
[2] Oita Univ, Sch Med, Inst Sci Res, Dept Life Sci, Oita 8795593, Japan
[3] Univ Tokushima, Dept Nutr & Metab, Tokushima 7708503, Japan
[4] Chiba Univ, Grad Sch Med, Dept Cardiovasc Sci & Med, Chiba 2608670, Japan
关键词
Csx/Nkx2.5; GATA4; L-type Ca2+ channel; T-type Ca2+ channel; hyperpolarization-activated cation (I-h) channels;
D O I
10.1016/j.yjmcc.2007.03.905
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The cardiac transcription factors Csx/Nkx2.5 and GATA4 play important roles in vertebrate heart development. Although mutations of Csx/ Nkx2.5 or GATA4 are associated with various congenital heart diseases, their mechanism of action on cardiomyocyte function is not completely elucidated. In this study, we therefore investigated the actions of these transcription factors on the electrophys io logical features and expression of ion channels in cardiomyocytes. Genes for transcription factors Csx/Nkx2.5 and GATA4 were transfected into rat neonatal cardiornyocytes by adenoviral infection. Action potentials, L-, T-type Ca2+ channels and hyperpolarization-activated cation current (I-h) of rat neonatal myocytes were recorded by patch clamp technique after adenoviral infection. Expression of ion channels was confirmed by real-time PCR. In Csx/Nkx2.5 overexpression inyocytes, the spontaneous beating rate was markedly increased with an up-regulation of the Ca(v)3.2 T-type Ca2+ channel, while in GATA4 overexpression myocytes, the T-type Ca2+ channel was unchanged. On the other hand, the L-type Ca 2+ channel was down-regulated by both Csx/Nkx2.5 and GATA4 overexpression; the level of Ca(v)1.3 mRNA was dramatically decreased by Csx/Nkx2.5 overexpression. These results indicate that Csx/Nkx2.5 and GATA4 play important roles on the generation of pacemaker potentials modulating voltage-dependent Ca2+ channels in the neonatal cardiomyocyte. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1045 / 1053
页数:9
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