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Increased lipid metabolism impairs NK cell function and mediates adaptation to the lymphoma environment.
Kobayashi, Takumi; Lam, Pui Yeng; Jiang, Hui; Bednarska, Karolina; Gloury, Renee; Murigneux, Valentine; Tay, Joshua; Jacquelot, Nicolas; Li, Rui; Tuong, Zewen Kelvin; Leggatt, Graham R; Gandhi, Maher K; Hill, Michelle M; Belz, Gabrielle T; Ngo, Shyuan; Kallies, Axel; Mattarollo, Stephen R.
Affiliation
  • Kobayashi T; University of Queensland Diamantina Institute and.
  • Lam PY; University of Queensland Diamantina Institute and.
  • Jiang H; University of Queensland Diamantina Institute and.
  • Bednarska K; Mater Research Institute, University of Queensland, Woolloongabba, QLD, Australia.
  • Gloury R; Peter Doherty Institute for Infection and Immunity, Department of Microbiology and Immunology, University of Melbourne, Melbourne, VIC, Australia.
  • Murigneux V; University of Queensland Diamantina Institute and.
  • Tay J; Mater Research Institute, University of Queensland, Woolloongabba, QLD, Australia.
  • Jacquelot N; Walter and Elisa Hall Institute of Medical Research, Parkville, VIC, Australia.
  • Li R; Department of Medical Biology, University of Melbourne, VIC, Australia.
  • Tuong ZK; Australian Institute for Bioengineering and Nanotechnology.
  • Leggatt GR; Queensland Brain Institute and.
  • Gandhi MK; School of Biomedical Sciences, University of Queensland, St Lucia, QLD, Australia.
  • Hill MM; University of Queensland Diamantina Institute and.
  • Belz GT; University of Queensland Diamantina Institute and.
  • Ngo S; Mater Research Institute, University of Queensland, Woolloongabba, QLD, Australia.
  • Kallies A; Department of Haematology, Princess Alexandra Hospital, Brisbane, QLD, Australia; and.
  • Mattarollo SR; University of Queensland Diamantina Institute and.
Blood ; 136(26): 3004-3017, 2020 12 24.
Article in En | MEDLINE | ID: mdl-32818230
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Killer Cells, Natural / Lymphoma, Large B-Cell, Diffuse / Lipid Metabolism / Tumor Microenvironment Limits: Animals / Humans Language: En Journal: Blood Year: 2020 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Killer Cells, Natural / Lymphoma, Large B-Cell, Diffuse / Lipid Metabolism / Tumor Microenvironment Limits: Animals / Humans Language: En Journal: Blood Year: 2020 Document type: Article Country of publication: United States