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dc.contributor.authorZeigerer, Anja
dc.contributor.authorBogorad, Roman L.
dc.contributor.authorSharma, Kirti
dc.contributor.authorGilleron, Jerome
dc.contributor.authorSeifert, Sarah
dc.contributor.authorSales, Susanne
dc.contributor.authorBerndt, Nikolaus
dc.contributor.authorBulik, Sascha
dc.contributor.authorMarsico, Giovanni
dc.contributor.authorD’Souza, Rochelle C.J.
dc.contributor.authorLakshmanaperumal, Naharajan
dc.contributor.authorMeganathan, Kesavan
dc.contributor.authorNatarajan, Karthick
dc.contributor.authorSachinidis, Agapios
dc.contributor.authorDahl, Andreas
dc.contributor.authorHolzhütter, Hermann-Georg
dc.contributor.authorShevchenko, Andrej
dc.contributor.authorMann, Matthias
dc.contributor.authorKoteliansky, Victor
dc.contributor.authorZerial, Marino
dc.contributor.authorBogorad, Roman
dc.date.accessioned2016-03-14T23:43:34Z
dc.date.available2016-03-14T23:43:34Z
dc.date.issued2015-04
dc.date.submitted2015-02
dc.identifier.issn22111247
dc.identifier.urihttp://hdl.handle.net/1721.1/101702
dc.description.abstractThe liver maintains glucose and lipid homeostasis by adapting its metabolic activity to the energy needs of the organism. Communication between hepatocytes and extracellular environment via endocytosis is key to such homeostasis. Here, we addressed the question of whether endosomes are required for gluconeogenic gene expression. We took advantage of the loss of endosomes in the mouse liver upon Rab5 silencing. Strikingly, we found hepatomegaly and severe metabolic defects such as hypoglycemia, hypercholesterolemia, hyperlipidemia, and glycogen accumulation that phenocopied those found in von Gierke’s disease, a glucose-6-phosphatase (G6Pase) deficiency. G6Pase deficiency alone can account for the reduction in hepatic glucose output and glycogen accumulation as determined by mathematical modeling. Interestingly, we uncovered functional alterations in the transcription factors, which regulate G6Pase expression. Our data highlight a requirement of Rab5 and the endosomal system for the regulation of gluconeogenic gene expression that has important implications for metabolic diseases.en_US
dc.description.sponsorshipGermany. Federal Ministry of Education and Researchen_US
dc.description.sponsorshipMax Planck Society for the Advancement of Scienceen_US
dc.description.sponsorshipDeutsche Forschungsgemeinschafen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.celrep.2015.04.018en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceElsevieren_US
dc.titleRegulation of Liver Metabolism by the Endosomal GTPase Rab5en_US
dc.typeArticleen_US
dc.identifier.citationZeigerer, Anja, Roman L. Bogorad, Kirti Sharma, Jerome Gilleron, Sarah Seifert, Susanne Sales, Nikolaus Berndt, et al. “Regulation of Liver Metabolism by the Endosomal GTPase Rab5.” Cell Reports 11, no. 6 (May 2015): 884–892.en_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorBogorad, Roman L.en_US
dc.relation.journalCell Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsZeigerer, Anja; Bogorad, Roman L.; Sharma, Kirti; Gilleron, Jerome; Seifert, Sarah; Sales, Susanne; Berndt, Nikolaus; Bulik, Sascha; Marsico, Giovanni; D’Souza, Rochelle C.J.; Lakshmanaperumal, Naharajan; Meganathan, Kesavan; Natarajan, Karthick; Sachinidis, Agapios; Dahl, Andreas; Holzhütter, Hermann-Georg; Shevchenko, Andrej; Mann, Matthias; Koteliansky, Victor; Zerial, Marinoen_US
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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