T cell immunoglobulin and mucin domain protein 3 inhibits glycolysis in RAW 264.7 macrophages through Hexokinase 2

Scand J Immunol. 2021 Feb;93(2):e12981. doi: 10.1111/sji.12981. Epub 2020 Oct 24.

Abstract

T cell immunoglobulin and mucin domain-3 (Tim-3), an immune checkpoint molecule, plays critical roles in maintaining innate immune homeostasis; however, the mechanisms underlying these roles remain to be determined. Here, we determined that Tim-3 controls glycolysis in macrophages and thus contributes to phenotype shifting. Tim-3 signal blockade significantly increases lactate production by macrophages, but does not influence cell proliferation or apoptosis. Tim-3 attenuates glucose uptake by inhibiting hexokinase 2 (HK2) expression in macrophages. Tim-3-mediated inhibition of macrophage glycolysis and the expression of proinflammatory cytokines, tumour necrosis factor (TNF)-α and interleukin (IL)-1β are reversed by HK2 silencing. Finally, we demonstrated that Tim-3 inhibits HK2 expression via the STAT1 pathway. We have thus discovered a new way by which Tim-3 modulates macrophage function.

Keywords: Tim-3; glycolysis; macrophage; metabolism.

MeSH terms

  • Animals
  • Apoptosis / immunology
  • Cell Line
  • Cell Proliferation / physiology
  • Cytokines / immunology
  • Glycolysis / immunology*
  • HEK293 Cells
  • Hepatitis A Virus Cellular Receptor 2 / immunology*
  • Hexokinase / immunology*
  • Humans
  • Immunity, Innate / immunology
  • Inflammation / immunology
  • Interleukin-1beta / immunology
  • Macrophages / immunology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • RAW 264.7 Cells
  • Signal Transduction / immunology*
  • T-Lymphocytes / immunology*
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Cytokines
  • Havcr2 protein, mouse
  • Hepatitis A Virus Cellular Receptor 2
  • Interleukin-1beta
  • Tumor Necrosis Factor-alpha
  • Hexokinase
  • hexokinase 2, mouse