Increased lipid metabolism impairs NK cell function and mediates adaptation to the lymphoma environment

Blood. 2020 Dec 24;136(26):3004-3017. doi: 10.1182/blood.2020005602.

Abstract

Natural killer (NK) cells play critical roles in protection against hematological malignancies but can acquire a dysfunctional state, which limits antitumor immunity. However, the underlying reasons for this impaired NK cell function remain to be uncovered. We found that NK cells in aggressive B-cell lymphoma underwent substantial transcriptional reprogramming associated with increased lipid metabolism, including elevated expression of the transcriptional regulator peroxisome activator receptor-γ (PPAR-γ). Exposure to fatty acids in the lymphoma environment potently suppressed NK cell effector response and cellular metabolism. NK cells from both diffuse large B-cell lymphoma patients and Eµ-myc B-cell lymphoma-bearing mice displayed reduced interferon-γ (IFN-γ) production. Activation of PPAR-γ partially restored mitochondrial membrane potential and IFN-γ production. Overall, our data indicate that increased lipid metabolism, while impairing their function, is a functional adaptation of NK cells to the fatty-acid rich lymphoma environment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Humans
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / pathology
  • Lipid Metabolism / immunology*
  • Lymphoma, Large B-Cell, Diffuse / genetics
  • Lymphoma, Large B-Cell, Diffuse / immunology*
  • Lymphoma, Large B-Cell, Diffuse / pathology
  • Membrane Potential, Mitochondrial / genetics
  • Membrane Potential, Mitochondrial / immunology
  • Mice
  • Mice, Transgenic
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / immunology
  • PPAR gamma / genetics
  • PPAR gamma / immunology
  • Tumor Microenvironment / genetics
  • Tumor Microenvironment / immunology*

Substances

  • IFNG protein, mouse
  • Neoplasm Proteins
  • PPAR gamma
  • Pparg protein, mouse
  • Interferon-gamma