Increases in intracellular sodium activate transcription and gene expression via the salt-inducible kinase 1 network in an atrial myocyte cell line

Cardiac hypertrophy (CH) generally occurs as the result of the sustained mechanical stress caused by elevated systemic arterial blood pressure (BP). However, in animal models, elevated salt intake is associated with CH even in the absence of significant increases in BP. We hypothesize that CH is not...

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Published inAmerican journal of physiology. Heart and circulatory physiology Vol. 302; no. 13; p. H57
Main Authors Popov, Sergej, Venetsanou, Kyriaki, Chedrese, P Jorge, Pinto, Vanda, Takemori, Hiroshi, Franco-Cereceda, Anders, Eriksson, Per, Mochizuki, Naoki, Soares-da-Silva, Patricio, Bertorello, Alejandro M
Format Journal Article
LanguageEnglish
Published Bethesda American Physiological Society 01.07.2012
Subjects
Blood pressure
Cardiovascular disease
Cells
Gene expression
Kinases
Physiology
Salt
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Summary:Cardiac hypertrophy (CH) generally occurs as the result of the sustained mechanical stress caused by elevated systemic arterial blood pressure (BP). However, in animal models, elevated salt intake is associated with CH even in the absence of significant increases in BP. We hypothesize that CH is not exclusively the consequence of mechanical stress but also of other factors associated with elevated BP such as abnormal cell sodium homeostasis. We examined the effect of small increases in intracellular sodium concentration ([Na+]i) on transcription factors and genes associated with CH in a cardiac cell line. Increases in [Na+]i led to a time-dependent increase in the expression levels of mRNA for natriuretic peptide and myosin heavy chain genes and also increased myocyte enhancer factor (MEF)2/nuclear factor of activated T cell (NFAT) transcriptional activity. Increases in [Na+]i are associated with activation of salt-inducible kinase 1 (snflk-1, SIK1), a kinase known to be critical for cardiac development. Moreover, increases in [Na+]i resulted in increased SIK1 expression. Sodium did not increase MEF2/NFAT activity or gene expression in cells expressing a SIK1 that lacked kinase activity. The mechanism by which SIK1 activated MEF2 involved phosphorylation of HDAC5. Increases in [Na+]i activate SIK1 and MEF2 via a parallel increase in intracellular calcium through the reverse mode of Na+/Ca2+-exchanger and activation of CaMK1. These data obtained in a cardiac cell line suggest that increases in intracellular sodium could influence myocardial growth by controlling transcriptional activation and gene expression throughout the activation of the SIK1 network. [PUBLICATION ABSTRACT]
ISSN:0363-6135
1522-1539