Ceramide and its metabolites modulate time-dependently the activity of the Na+/K+ ATPase in HepG2 cells
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Elsevier Ltd
Abstract
Ceramide is involved in the regulation of many cellular processes including cell proliferation and apoptosis, which are accompanied respectively with a decrease and an increase in the activity of the Na+/K+ ATPase. These antagonistic effects may be time-dependent and due to different signaling pathways requiring different time intervals to be activated. While we showed previously a ceramide-induced inhibition of the ATPase in HepG2 cells during the first hour, we study here the effect of ceramide thereafter. Ceramide stimulated the Na+/K+ ATPase between 1 and 4 h with a peak at 2 h. This stimulation was maintained in the simultaneous presence of an inhibitor of ceramidase (CAY 10466) but disappeared when ceramide kinase was inhibited, suggesting a role of ceramide-1-phosphate (cer-1-P) in the observed effect. Exogenous cer-1-P caused a similar stimulation of the ATPase which was not affected by an inhibition of JNK but changed into a decrease in presence of PDTC, a specific inhibitor of NF-κB, and disappeared when NF-κB and JNK were inhibited simultaneously. It was concluded that cer-1-P activates both JNK and NF-κB. While JNK exerts an inhibitory effect on the ATPase, NF-κB increases its activity and abrogates the stimulatory effect of the sphingolipid on JNK leading thus to an additional increase in the ATPase activity. © 2014 Elsevier Ltd.
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Ceramide, Ceramide one phosphate, Jnk, Nf-κb, Apoptosis, Caspases, Ceramides, Hep g2 cells, Humans, Jnk mitogen-activated protein kinases, Nf-kappa b, Phosphotransferases (alcohol group acceptor), Signal transduction, Sodium-potassium-exchanging atpase, Adenosine triphosphatase, Adenosine triphosphatase (potassium sodium), Anthra[1,9 cd]pyrazol 6(2h) one, Cay 10466, Ceramide 1 phosphate, Ceramide kinase, Hydrolase inhibitor, Immunoglobulin enhancer binding protein, N [ 2 hydroxy 1 (hydroxymethyl) 2 ( 4 nitrophenyl)ethyl]tetradecanamide, Pyrrolidine dithiocarbamate, Sphingolipid, Stress activated protein kinase, Unclassified drug, Caspase, Ceramide 1-phosphate, Phosphotransferase, Article, Cell stimulation, Cell survival, Controlled study, Drug effect, Enzyme activity, Enzyme inhibition, Hepg2 cell line, Human, Human cell, Human cell culture, In vitro study, Metabolite, Protein conformation, Protein function, Time, Antagonists and inhibitors, Biosynthesis, Drug effects, Genetics, Metabolism