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Association of TIM-3 expression with glucose metabolism in Jurkat T cells
DC Field | Value | Language |
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dc.contributor.author | Lee, MJ | - |
dc.contributor.author | Yun, SJ | - |
dc.contributor.author | Lee, B | - |
dc.contributor.author | Jeong, E | - |
dc.contributor.author | Yoon, G | - |
dc.contributor.author | Kim, K | - |
dc.contributor.author | Park, S | - |
dc.date.accessioned | 2022-11-29T01:43:34Z | - |
dc.date.available | 2022-11-29T01:43:34Z | - |
dc.date.issued | 2020 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/23022 | - |
dc.description.abstract | BACKGROUND: 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.iso | en | - |
dc.subject.MESH | CD4-Positive T-Lymphocytes | - |
dc.subject.MESH | Gene Expression Regulation | - |
dc.subject.MESH | Gene Knockdown Techniques | - |
dc.subject.MESH | Glucose | - |
dc.subject.MESH | Glucose Transporter Type 1 | - |
dc.subject.MESH | Glutamine | - |
dc.subject.MESH | Hepatitis A Virus Cellular Receptor 2 | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Jurkat Cells | - |
dc.subject.MESH | Lymphocyte Activation | - |
dc.subject.MESH | Membrane Potentials | - |
dc.subject.MESH | Reactive Oxygen Species | - |
dc.title | Association of TIM-3 expression with glucose metabolism in Jurkat T cells | - |
dc.type | Article | - |
dc.identifier.pmid | 32819283 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441550 | - |
dc.subject.keyword | HAVCR2 | - |
dc.subject.keyword | Glycolysis | - |
dc.subject.keyword | CD4+ T cell | - |
dc.subject.keyword | Glutaminolysis | - |
dc.subject.keyword | Glucose transporter | - |
dc.contributor.affiliatedAuthor | Yoon, G | - |
dc.contributor.affiliatedAuthor | Kim, K | - |
dc.contributor.affiliatedAuthor | Park, S | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1186/s12865-020-00377-6 | - |
dc.citation.title | BMC immunology | - |
dc.citation.volume | 21 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2020 | - |
dc.citation.startPage | 48 | - |
dc.citation.endPage | 48 | - |
dc.identifier.bibliographicCitation | BMC immunology, 21(1). : 48-48, 2020 | - |
dc.identifier.eissn | 1471-2172 | - |
dc.relation.journalid | J014712172 | - |
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