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

BMC Immunol. 2020 Aug 20;21(1):48. doi: 10.1186/s12865-020-00377-6.

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.

Keywords: CD4+ T cell; Glucose transporter; Glutaminolysis; Glycolysis; HAVCR2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD4-Positive T-Lymphocytes / immunology*
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Glucose / metabolism*
  • Glucose Transporter Type 1 / genetics
  • Glucose Transporter Type 1 / metabolism
  • Glutamine / metabolism
  • Hepatitis A Virus Cellular Receptor 2 / genetics
  • Hepatitis A Virus Cellular Receptor 2 / metabolism*
  • Humans
  • Jurkat Cells
  • Lymphocyte Activation
  • Membrane Potentials
  • Reactive Oxygen Species / metabolism

Substances

  • Glucose Transporter Type 1
  • HAVCR2 protein, human
  • Hepatitis A Virus Cellular Receptor 2
  • Reactive Oxygen Species
  • Glutamine
  • Glucose