| Literature DB >> 32818230 |
Takumi Kobayashi1, Pui Yeng Lam1, Hui Jiang1, Karolina Bednarska2, Renee Gloury3, Valentine Murigneux1, Joshua Tay2, Nicolas Jacquelot4,5, Rui Li6,7,8, Zewen Kelvin Tuong1, Graham R Leggatt1, Maher K Gandhi2,9, Michelle M Hill1,10, Gabrielle T Belz4,5, Shyuan Ngo6,7,8, Axel Kallies3,4, Stephen R Mattarollo1.
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.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32818230 DOI: 10.1182/blood.2020005602
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113