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dc.contributor.authorPetit, Lolita
dc.contributor.authorMa, Shan
dc.contributor.authorCipi, Joris
dc.contributor.authorCheng, Shun-Yun
dc.contributor.authorZieger, Marina
dc.contributor.authorHay, Nissim
dc.contributor.authorPunzo, Claudio
dc.date2022-08-11T08:09:50.000
dc.date.accessioned2022-08-23T16:45:28Z
dc.date.available2022-08-23T16:45:28Z
dc.date.issued2018-05-29
dc.date.submitted2018-07-27
dc.identifier.citation<p>Cell Rep. 2018 May 29;23(9):2629-2642. doi: 10.1016/j.celrep.2018.04.111. <a href="https://doi.org/10.1016/j.celrep.2018.04.111">Link to article on publisher's site</a></p>
dc.identifier.issn2211-1247 (Electronic)
dc.identifier.doi10.1016/j.celrep.2018.04.111
dc.identifier.pmid29847794
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40688
dc.description.abstractAerobic glycolysis accounts for approximately 80%-90% of glucose used by adult photoreceptors (PRs); yet, the importance of aerobic glycolysis for PR function or survival remains unclear. Here, we further established the role of aerobic glycolysis in murine rod and cone PRs. We show that loss of hexokinase-2 (HK2), a key aerobic glycolysis enzyme, does not affect PR survival or structure but is required for normal rod function. Rods with HK2 loss increase their mitochondrial number, suggesting an adaptation to the inhibition of aerobic glycolysis. In contrast, cones adapt without increased mitochondrial number but require HK2 to adapt to metabolic stress conditions such as those encountered in retinitis pigmentosa, where the loss of rods causes a nutrient shortage in cones. The data support a model where aerobic glycolysis in PRs is not a necessity but rather a metabolic choice that maximizes PR function and adaptability to nutrient stress conditions.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=29847794&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsThis is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAerobic glycolysis
dc.subjectcones
dc.subjecthexokinase-2
dc.subjectmetabolic coupling
dc.subjectoxidative phosphorylation
dc.subjectretinitis pigmentosa
dc.subjectrod metabolism
dc.subjectrods
dc.subjectCellular and Molecular Physiology
dc.subjectEye Diseases
dc.subjectOphthalmology
dc.titleAerobic Glycolysis Is Essential for Normal Rod Function and Controls Secondary Cone Death in Retinitis Pigmentosa
dc.typeJournal Article
dc.source.journaltitleCell reports
dc.source.volume23
dc.source.issue9
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4501&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3490
dc.identifier.contextkey12556174
refterms.dateFOA2022-08-23T16:45:28Z
html.description.abstract<p>Aerobic glycolysis accounts for approximately 80%-90% of glucose used by adult photoreceptors (PRs); yet, the importance of aerobic glycolysis for PR function or survival remains unclear. Here, we further established the role of aerobic glycolysis in murine rod and cone PRs. We show that loss of hexokinase-2 (HK2), a key aerobic glycolysis enzyme, does not affect PR survival or structure but is required for normal rod function. Rods with HK2 loss increase their mitochondrial number, suggesting an adaptation to the inhibition of aerobic glycolysis. In contrast, cones adapt without increased mitochondrial number but require HK2 to adapt to metabolic stress conditions such as those encountered in retinitis pigmentosa, where the loss of rods causes a nutrient shortage in cones. The data support a model where aerobic glycolysis in PRs is not a necessity but rather a metabolic choice that maximizes PR function and adaptability to nutrient stress conditions.</p>
dc.identifier.submissionpathoapubs/3490
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Pediatrics, Division of Pulmonary Medicine
dc.contributor.departmentGene Therapy Center
dc.contributor.departmentDepartment of Ophthalmology
dc.source.pages2629-2642


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This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).