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Association of TIM-3 expression with glucose metabolism in Jurkat T cells
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 regula...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441550/ https://www.ncbi.nlm.nih.gov/pubmed/32819283 http://dx.doi.org/10.1186/s12865-020-00377-6 |
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author | Lee, Mi Jin Yun, Su Jin Lee, Bokyoung Jeong, Eun Yoon, Gyesoon Kim, Kyongmin Park, Sun |
author_facet | Lee, Mi Jin Yun, Su Jin Lee, Bokyoung Jeong, Eun Yoon, Gyesoon Kim, Kyongmin Park, Sun |
author_sort | Lee, Mi Jin |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7441550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74415502020-08-24 Association of TIM-3 expression with glucose metabolism in Jurkat T cells Lee, Mi Jin Yun, Su Jin Lee, Bokyoung Jeong, Eun Yoon, Gyesoon Kim, Kyongmin Park, Sun BMC Immunol Research Article 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. BioMed Central 2020-08-20 /pmc/articles/PMC7441550/ /pubmed/32819283 http://dx.doi.org/10.1186/s12865-020-00377-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Lee, Mi Jin Yun, Su Jin Lee, Bokyoung Jeong, Eun Yoon, Gyesoon Kim, Kyongmin Park, Sun Association of TIM-3 expression with glucose metabolism in Jurkat T cells |
title | Association of TIM-3 expression with glucose metabolism in Jurkat T cells |
title_full | Association of TIM-3 expression with glucose metabolism in Jurkat T cells |
title_fullStr | Association of TIM-3 expression with glucose metabolism in Jurkat T cells |
title_full_unstemmed | Association of TIM-3 expression with glucose metabolism in Jurkat T cells |
title_short | Association of TIM-3 expression with glucose metabolism in Jurkat T cells |
title_sort | association of tim-3 expression with glucose metabolism in jurkat t cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441550/ https://www.ncbi.nlm.nih.gov/pubmed/32819283 http://dx.doi.org/10.1186/s12865-020-00377-6 |
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