Cited time in webofscience Cited time in scopus

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dc.contributor.author Kim, Eun Seon -
dc.contributor.author Kim, Kyu-Sung -
dc.contributor.author Lee, Chan Hee -
dc.contributor.author Jeon, Min-Tae -
dc.contributor.author Lee, Sung Bae -
dc.contributor.author Lee, Jong Hwa -
dc.contributor.author Kim, Do-Geun -
dc.date.accessioned 2022-09-30T07:30:00Z -
dc.date.available 2022-09-30T07:30:00Z -
dc.date.created 2022-05-31 -
dc.date.issued 2022-07 -
dc.identifier.issn 0893-7648 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/16878 -
dc.description.abstract Among the components of the blood-brain barrier (BBB), endothelial cells (ECs) play an important role in supplying limited materials, especially glucose, to the brain. However, the mechanism by which glucose is metabolized in brain ECs is still elusive. To address this topic, we assessed the metabolic signature of glucose utilization using live-cell metabolic assays and liquid chromatography-tandem mass spectrometry metabolomic analysis. We found that brain ECs are highly dependent on aerobic glycolysis, generating lactate as its final product with minimal consumption of glucose. Glucose treatment decreased the oxygen consumption rate in a dose-dependent manner, indicating the Crabtree effect. Moreover, when glycolysis was inhibited, brain ECs showed impaired permeability to molecules utilizing transcellular pathway. In addition, we found that the blockade of glycolysis in mouse brain with 2-deoxyglucose administration resulted in decreased transcellular permeability of the BBB. In conclusion, utilizing glycolysis in brain ECs has critical roles in the maintenance and permeability of the BBB. Overall, we could conclude that brain ECs are highly glycolytic, and their energy can be used to maintain the transcellular permeability of the BBB. -
dc.language English -
dc.publisher Humana Press, Inc. -
dc.title Brain Endothelial Cells Utilize Glycolysis for the Maintenance of the Transcellular Permeability -
dc.type Article -
dc.identifier.doi 10.1007/s12035-022-02778-7 -
dc.identifier.wosid 000790638200001 -
dc.identifier.scopusid 2-s2.0-85129646071 -
dc.identifier.bibliographicCitation Molecular Neurobiology, v.59, no.7, pp.4315 - 4333 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordAuthor Energy metabolism -
dc.subject.keywordAuthor Transcytosis -
dc.subject.keywordAuthor Endothelial cells -
dc.subject.keywordAuthor Glucose -
dc.subject.keywordAuthor BBB -
dc.subject.keywordPlus AEROBIC GLYCOLYSIS -
dc.subject.keywordPlus GLUCOSE -
dc.subject.keywordPlus METABOLISM -
dc.subject.keywordPlus LACTATE -
dc.subject.keywordPlus CANCER -
dc.subject.keywordPlus TRANSCYTOSIS -
dc.subject.keywordPlus PENETRATION -
dc.subject.keywordPlus MECHANISM -
dc.subject.keywordPlus GLUTAMINE -
dc.subject.keywordPlus NUTRIENT -
dc.citation.endPage 4333 -
dc.citation.number 7 -
dc.citation.startPage 4315 -
dc.citation.title Molecular Neurobiology -
dc.citation.volume 59 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Neurosciences & Neurology -
dc.relation.journalWebOfScienceCategory Neurosciences -
dc.type.docType Article -
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Department of Brain Sciences Laboratory of Neurodegenerative Diseases and Aging 1. Journal Articles

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