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dc.contributor.authorGubern, Albert
dc.contributor.authorBarceló-Torns, Miquel
dc.contributor.authorCasas, Javier
dc.contributor.authorBarneda, David
dc.contributor.authorMasgrau, Roser
dc.contributor.authorPicatoste, Fernando
dc.contributor.authorBalsinde, Jesús
dc.contributor.authorBalboa, María A.
dc.contributor.authorClaro, Enrique
dc.date.accessioned2024-01-08T14:16:25Z
dc.date.available2024-01-08T14:16:25Z
dc.date.issued2009
dc.identifier.citationThe Journal of biological chemistry 284, 5697–5708 (2009).es
dc.identifier.issn0021-9258es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/64295
dc.descriptionProducción Científicaes
dc.description.abstractThis work investigates the metabolic origin of triacylglycerol (TAG) formed during lipid droplet (LD) biogenesis induced by stress. Cytotoxic inhibitors of fatty acid synthase induced TAG synthesis and LD biogenesis in CHO-K1 cells, in the absence of external sources of fatty acids. TAG synthesis was required for LD biogenesis and was sensitive to inhibition and down-regulation of the expression of group VIA phospholipase A(2) (iPLA(2)-VIA). Induction of stress with acidic pH, C(2)-ceramide, tunicamycin, or deprivation of glucose also stimulated TAG synthesis and LD formation in a manner dependent on iPLA(2)-VIA. Overexpression of the enzyme enhanced TAG synthesis from endogenous fatty acids and LD occurrence. During stress, LD biogenesis but not TAG synthesis required phosphorylation and activation of group IVA PLA(2) (cPLA(2)alpha). The results demonstrate that iPLA(2)-VIA provides fatty acids for TAG synthesis while cPLA(2)alpha allows LD biogenesis. LD biogenesis during stress may be a survival strategy, recycling structural phospholipids into energy-generating substrates.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleLipid Droplet Biogenesis Induced by Stress Involves Triacylglycerol Synthesis That Depends on Group VIA Phospholipase A2es
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1074/jbc.m806173200es
dc.identifier.publicationfirstpage5697es
dc.identifier.publicationissue9es
dc.identifier.publicationlastpage5708es
dc.identifier.publicationtitleJournal of Biological Chemistryes
dc.identifier.publicationvolume284es
dc.peerreviewedSIes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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