Yu, Liangzhu, Gao, Shijun, Nie, Li, Tang, Ming, Huang, Weifeng, Luo, Hongyan, Hu, Xinwu, Xi, Jiaoya, Zhu, Minjie, Zheng, Yunjie, Gao, Linlin, Zhang, Lanqiu, Song, Yuanlong, Hescheler, Juergen and Liang, Huamin (2011). Molecular and Functional Changes in Voltage-Gated Na+ Channels in Cardiomyocytes During Mouse Embryogenesis. Circ. J., 75 (9). S. 2071 - 2080. TOYKO: JAPANESE CIRCULATION SOC. ISSN 1347-4820

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Abstract

Background: Embryonic cardiomyocytes undergo profound changes in their electrophysiological properties during development. However, the molecular and functional changes in Na+ channel during cardiogenesis are not yet fully explained. Methods and Results: To study the functional changes in the Na+ channel during cardiogenesis, Na+ currents were recorded in the early (EDS) and late (LDS) developmental stages of cardiomyocytes in embryonic mice. Compared with EDS myocytes, LDS myocytes exhibited a larger peak current density, a more negative shift in the voltage of half inactivation, a larger fast inactivation component and a smaller slow inactivation component, and smaller time constants for recovery from inactivation. Additionally, multiple Na+ channel alpha-subunits (Nay 1.1-1.6) and beta-subunits (Nay beta 1-beta 3) of mouse embryos were investigated. Transcripts of Nay 1.1-1.3 were absent or present at very low levels in embryonic hearts. Transcripts encoding Nay 1.4-1.6 and Nay beta 1-beta 3 increased during embryogenesis. Data on the sensitivity of total Na+ currents to tetrodotoxin (TTX) showed that TTX-resistant Nay 1.5 is the predominant isoform expressed in the heart of the mouse embryo. Conclusions: The results indicate that significant changes in the functional properties of Na+ channels develop in the cardiomyocytes of the mouse embryo, and that different Na+ channel subunit genes are strongly regulated during embryogenesis, which further support a physiological role for voltage-gated Na+ channels during heart development. (Circ J 2011; 75: 2071-2079)

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Yu, LiangzhuUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Gao, ShijunUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nie, LiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Tang, MingUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Huang, WeifengUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Luo, HongyanUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hu, XinwuUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Xi, JiaoyaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Zhu, MinjieUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Zheng, YunjieUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Gao, LinlinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Zhang, LanqiuUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Song, YuanlongUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hescheler, JuergenUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Liang, HuaminUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-489927
DOI: 10.1253/circj.CJ-10-1212
Journal or Publication Title: Circ. J.
Volume: 75
Number: 9
Page Range: S. 2071 - 2080
Date: 2011
Publisher: JAPANESE CIRCULATION SOC
Place of Publication: TOYKO
ISSN: 1347-4820
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
NEURONAL SODIUM-CHANNELS; DIFFERENT GATING MODES; DEVELOPMENTAL-CHANGES; VENTRICULAR MYOCYTES; EXPRESSION PATTERN; MAMMALIAN-CELLS; PURKINJE-FIBERS; XENOPUS OOCYTES; STEM-CELLS; I-FMultiple languages
Cardiac & Cardiovascular SystemsMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/48992

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