Ceramide and its metabolites modulate time-dependently the activity of the Na+/K+ ATPase in HepG2 cells

dc.contributor.authorKreydiyyeh, Sawsan Ibrahim
dc.contributor.authorDakroub, Zeina
dc.contributor.departmentDepartment of Biology
dc.contributor.facultyFaculty of Arts and Sciences (FAS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:20:30Z
dc.date.available2025-01-24T11:20:30Z
dc.date.issued2014
dc.description.abstractCeramide 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.
dc.identifier.doihttps://doi.org/10.1016/j.biocel.2014.04.027
dc.identifier.eid2-s2.0-84901762310
dc.identifier.pmid24819540
dc.identifier.urihttp://hdl.handle.net/10938/25016
dc.language.isoen
dc.publisherElsevier Ltd
dc.relation.ispartofInternational Journal of Biochemistry and Cell Biology
dc.sourceScopus
dc.subjectCeramide
dc.subjectCeramide one phosphate
dc.subjectJnk
dc.subjectNf-κb
dc.subjectApoptosis
dc.subjectCaspases
dc.subjectCeramides
dc.subjectHep g2 cells
dc.subjectHumans
dc.subjectJnk mitogen-activated protein kinases
dc.subjectNf-kappa b
dc.subjectPhosphotransferases (alcohol group acceptor)
dc.subjectSignal transduction
dc.subjectSodium-potassium-exchanging atpase
dc.subjectAdenosine triphosphatase
dc.subjectAdenosine triphosphatase (potassium sodium)
dc.subjectAnthra[1,9 cd]pyrazol 6(2h) one
dc.subjectCay 10466
dc.subjectCeramide 1 phosphate
dc.subjectCeramide kinase
dc.subjectHydrolase inhibitor
dc.subjectImmunoglobulin enhancer binding protein
dc.subjectN [ 2 hydroxy 1 (hydroxymethyl) 2 ( 4 nitrophenyl)ethyl]tetradecanamide
dc.subjectPyrrolidine dithiocarbamate
dc.subjectSphingolipid
dc.subjectStress activated protein kinase
dc.subjectUnclassified drug
dc.subjectCaspase
dc.subjectCeramide 1-phosphate
dc.subjectPhosphotransferase
dc.subjectArticle
dc.subjectCell stimulation
dc.subjectCell survival
dc.subjectControlled study
dc.subjectDrug effect
dc.subjectEnzyme activity
dc.subjectEnzyme inhibition
dc.subjectHepg2 cell line
dc.subjectHuman
dc.subjectHuman cell
dc.subjectHuman cell culture
dc.subjectIn vitro study
dc.subjectMetabolite
dc.subjectProtein conformation
dc.subjectProtein function
dc.subjectTime
dc.subjectAntagonists and inhibitors
dc.subjectBiosynthesis
dc.subjectDrug effects
dc.subjectGenetics
dc.subjectMetabolism
dc.titleCeramide and its metabolites modulate time-dependently the activity of the Na+/K+ ATPase in HepG2 cells
dc.typeArticle

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