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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.
Afiliação
  • Lee MJ; Department of Microbiology, Ajou University School of Medicine, Suwon, 442-749, South Korea.
  • Yun SJ; Department of Microbiology, Ajou University School of Medicine, Suwon, 442-749, South Korea.
  • Lee B; Department of Biomedical Sciences, The Graduate School, Ajou University, Suwon, 442-749, South Korea.
  • Jeong E; Department of Microbiology, Ajou University School of Medicine, Suwon, 442-749, South Korea.
  • Yoon G; Department of Biomedical Sciences, The Graduate School, Ajou University, Suwon, 442-749, South Korea.
  • Kim K; Department of Microbiology, Ajou University School of Medicine, Suwon, 442-749, South Korea.
  • Park S; Department of Biomedical Sciences, The Graduate School, Ajou University, Suwon, 442-749, South Korea.
BMC Immunol ; 21(1): 48, 2020 08 20.
Article em En | MEDLINE | ID: mdl-32819283
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T CD4-Positivos / Receptor Celular 2 do Vírus da Hepatite A / Glucose Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: BMC Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T CD4-Positivos / Receptor Celular 2 do Vírus da Hepatite A / Glucose Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: BMC Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Coréia do Sul