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Association of TIM-3 expression with glucose metabolism in Jurkat T cells

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dc.contributor.authorLee, MJ-
dc.contributor.authorYun, SJ-
dc.contributor.authorLee, B-
dc.contributor.authorJeong, E-
dc.contributor.authorYoon, G-
dc.contributor.authorKim, K-
dc.contributor.authorPark, S-
dc.date.accessioned2022-11-29T01:43:34Z-
dc.date.available2022-11-29T01:43:34Z-
dc.date.issued2020-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/23022-
dc.description.abstractBACKGROUND: T cell activation is associated with increase in glycolysis and glutaminolysis. T cell immunoglobulin and mucin domain containing protein-3 (TIM-3), a T cell surface molecule, downregulates T cell activation and leads to insufficient immunity in cancer and chronic infection. TIM-3 regulates T cell activation possibly through alterations in metabolism; however, the relationship between TIM-3 expression and T cell metabolic changes has not been well studied. RESULTS: We investigated the association between TIM-3 expression and metabolic changes by analyzing glucose metabolism, glutamine metabolism, and mitochondrial function in TIM-3 overexpressing or knockout Jurkat T cell lines relative to their control cell lines. Glucose uptake and consumption, and lactate release were downregulated by TIM-3 expression but upregulated by TIM-3 knockout. Concomitantly, the expression of the glucose transporter, Glut1, but not Glut2, 3, or 4 was altered by TIM-3 expression. However, TIM-3 expression alone could not account for the change in glutamine consumption, glutamate release, and mitochondrial mass, ROS production or membrane potential in these cell lines. CONCLUSION: Our results show the association of TIM-3 expression with T cell glucose metabolism. These results are significant in chronic infections and cancers where it is necessary to control TIM-3 expressing T cells.-
dc.language.isoen-
dc.subject.MESHCD4-Positive T-Lymphocytes-
dc.subject.MESHGene Expression Regulation-
dc.subject.MESHGene Knockdown Techniques-
dc.subject.MESHGlucose-
dc.subject.MESHGlucose Transporter Type 1-
dc.subject.MESHGlutamine-
dc.subject.MESHHepatitis A Virus Cellular Receptor 2-
dc.subject.MESHHumans-
dc.subject.MESHJurkat Cells-
dc.subject.MESHLymphocyte Activation-
dc.subject.MESHMembrane Potentials-
dc.subject.MESHReactive Oxygen Species-
dc.titleAssociation of TIM-3 expression with glucose metabolism in Jurkat T cells-
dc.typeArticle-
dc.identifier.pmid32819283-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441550-
dc.subject.keywordHAVCR2-
dc.subject.keywordGlycolysis-
dc.subject.keywordCD4+ T cell-
dc.subject.keywordGlutaminolysis-
dc.subject.keywordGlucose transporter-
dc.contributor.affiliatedAuthorYoon, G-
dc.contributor.affiliatedAuthorKim, K-
dc.contributor.affiliatedAuthorPark, S-
dc.type.localJournal Papers-
dc.identifier.doi10.1186/s12865-020-00377-6-
dc.citation.titleBMC immunology-
dc.citation.volume21-
dc.citation.number1-
dc.citation.date2020-
dc.citation.startPage48-
dc.citation.endPage48-
dc.identifier.bibliographicCitationBMC immunology, 21(1). : 48-48, 2020-
dc.identifier.eissn1471-2172-
dc.relation.journalidJ014712172-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Biochemistry & Molecular Biology
Journal Papers > School of Medicine / Graduate School of Medicine > Microbiology
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