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

Author:

Kobayashi Takumi1ORCID,Lam Pui Yeng1ORCID,Jiang Hui1ORCID,Bednarska Karolina2ORCID,Gloury Renee3,Murigneux Valentine1ORCID,Tay Joshua2ORCID,Jacquelot Nicolas45ORCID,Li Rui678,Tuong Zewen Kelvin1ORCID,Leggatt Graham R.1ORCID,Gandhi Maher K.29ORCID,Hill Michelle M.110ORCID,Belz Gabrielle T.45ORCID,Ngo Shyuan678ORCID,Kallies Axel34ORCID,Mattarollo Stephen R.1

Affiliation:

1. University of Queensland Diamantina Institute and

2. Mater Research Institute, University of Queensland, Woolloongabba, QLD, Australia;

3. Peter Doherty Institute for Infection and Immunity, Department of Microbiology and Immunology, University of Melbourne, Melbourne, VIC, Australia;

4. Walter and Elisa Hall Institute of Medical Research, Parkville, VIC, Australia;

5. Department of Medical Biology, University of Melbourne, VIC, Australia;

6. Australian Institute for Bioengineering and Nanotechnology,

7. Queensland Brain Institute and

8. School of Biomedical Sciences, University of Queensland, St Lucia, QLD, Australia;

9. Department of Haematology, Princess Alexandra Hospital, Brisbane, QLD, Australia; and

10. QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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