Renal L-2-hydroxyglutarate dehydrogenase activity promotes hypoxia tolerance and mitochondrial metabolism in Drosophila melanogaster

dc.contributor.authorMahmoudzadeh, Nader H.
dc.contributor.authorHeidarian, Yasaman
dc.contributor.authorTourigny, Jason P.
dc.contributor.authorFitt, Alexander J.
dc.contributor.authorBeebe, Katherine
dc.contributor.authorLi, Hongde
dc.contributor.authorLuhur, Arthur
dc.contributor.authorBuddika, Kasun
dc.contributor.authorMungcal, Liam
dc.contributor.authorKundu, Anirban
dc.contributor.authorPolicastro, Robert A.
dc.contributor.authorBrinkley, Garrett J.
dc.contributor.authorZentner, Gabriel E.
dc.contributor.authorNemkov, Travis
dc.contributor.authorPepin, Robert
dc.contributor.authorChawla, Geetanjali
dc.contributor.authorSudarshan, Sunil
dc.contributor.authorRodan, Aylin R.
dc.contributor.authorD’Alessandro, Angelo
dc.contributor.authorTennessen, Jason M.
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-10-29T13:05:45Z
dc.date.available2024-10-29T13:05:45Z
dc.date.issued2024
dc.description.abstractObjectives: The mitochondrial enzyme L-2-hydroxyglutarate dehydrogenase (L2HGDH) regulates the abundance of L-2-hydroxyglutarate (L-2HG), a potent signaling metabolite capable of influencing chromatin architecture, mitochondrial metabolism, and cell fate decisions. Loss of L2hgdh activity in humans induces ectopic L-2HG accumulation, resulting in neurodevelopmental defects, altered immune cell function, and enhanced growth of clear cell renal cell carcinomas. To better understand the molecular mechanisms that underlie these disease pathologies, we used the fruit fly Drosophila melanogaster to investigate the endogenous functions of L2hgdh. Methods: L2hgdh mutant adult male flies were analyzed under normoxic and hypoxic conditions using a combination of semi-targeted metabolomics and RNA-seq. These multi-omic analyses were complemented by tissue-specific genetic studies that examined the effects of L2hgdh mutations on the Drosophila renal system (Malpighian tubules; MTs). Results: Our studies revealed that while L2hgdh is not essential for growth or viability under standard culture conditions, L2hgdh mutants are hypersensitive to hypoxia and expire during the reoxygenation phase with severe disruptions of mitochondrial metabolism. Moreover, we find that the fly renal system is a key site of L2hgdh activity, as L2hgdh mutants that express a rescuing transgene within the MTs survive hypoxia treatment and exhibit normal levels of mitochondrial metabolites. We also demonstrate that even under normoxic conditions, L2hgdh mutant MTs experience significant metabolic stress and are sensitized to aberrant growth upon Egfr activation. Conclusions: These findings present a model in which renal L2hgdh activity limits systemic L-2HG accumulation, thus indirectly regulating the balance between glycolytic and mitochondrial metabolism, enabling successful recovery from hypoxia exposure, and ensuring renal tissue integrity.
dc.eprint.versionFinal published version
dc.identifier.citationMahmoudzadeh NH, Heidarian Y, Tourigny JP, et al. Renal L-2-hydroxyglutarate dehydrogenase activity promotes hypoxia tolerance and mitochondrial metabolism in Drosophila melanogaster. Mol Metab. 2024;89:102013. doi:10.1016/j.molmet.2024.102013
dc.identifier.urihttps://hdl.handle.net/1805/44322
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.molmet.2024.102013
dc.relation.journalMolecular Metabolism
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePMC
dc.subjectDrosophila
dc.subjectHypoxia
dc.subjectL-2-hydroxyglutarate
dc.subjectL2hgdh oncometabolite
dc.titleRenal L-2-hydroxyglutarate dehydrogenase activity promotes hypoxia tolerance and mitochondrial metabolism in Drosophila melanogaster
dc.typeArticle
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