Lactate dehydrogenase A-dependent aerobic glycolysis promotes natural killer cell anti-viral and anti-tumor function

被引:70
|
作者
Sheppard, Sam [1 ]
Santosa, Endi K. [1 ,2 ]
Lau, Colleen M. [1 ]
Violante, Sara [3 ]
Giovanelli, Paolo [1 ,2 ]
Kim, Hyunu [1 ]
Cross, Justin R. [3 ]
Li, Ming O. [1 ,2 ]
Sun, Joseph C. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Immunol Program, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Grad Sch Med Sci, Immunol & Microbial Pathogenesis Program, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Donald B & Catherine C Marron Canc Metab Ctr, New York, NY 10065 USA
来源
CELL REPORTS | 2021年 / 35卷 / 09期
关键词
MURINE CYTOMEGALOVIRUS; ACTIVATION RECEPTOR; LACTIC-ACID; RECOGNITION; MECHANISMS; GENERATION; INHIBITION; EXPRESSION; RESPONSES;
D O I
10.1016/j.celrep.2021.109210
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Natural killer (NK) cells are cytotoxic lymphocytes capable of rapid cytotoxicity, cytokine secretion, and clonal expansion. To sustain such energetically demanding processes, NK cells must increase their metabolic capacity upon activation. However, little is known about the metabolic requirements specific to NK cells in vivo. To gain greater insight, we investigated the role of aerobic glycolysis in NK cell function and demonstrate that their glycolytic rate increases rapidly following viral infection and inflammation, prior to that of CD8(+) T cells. NK cell-specific deletion of lactate dehydrogenase A (LDHA) reveals that activated NK cells rely on this enzyme for both effector function and clonal proliferation, with the latter being shared with T cells. As a result, LDHA-deficient NK cells are defective in their anti-viral and anti-tumor protection. These findings suggest that aerobic glycolysis is a hallmark of NK cell activation that is key to their function.
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页数:16
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