NAD+激酶
生物化学
谷氨酰胺分解
胞浆
分解代谢
生物
CD8型
化学
新陈代谢
酶
柠檬酸循环
免疫系统
免疫学
作者
Nina Weisshaar,Sicong Ma,Yanan Ming,Alaa Madi,Alessa Mieg,Marvin Hering,Ferdinand Zettl,Kerstin Möhr,Nora ten Bosch,Diana Stichling,Michael Buettner,Gernot Poschet,Glynis Klinke,Michael Schulz,Nina Kunze-Rohrbach,Carolin Kerber,Isabel Madeleine Klein,Jingxia Wu,Xi Wang,Guoliang Cui
出处
期刊:Nature Immunology
[Nature Portfolio]
日期:2023-10-09
卷期号:24 (11): 1921-1932
被引量:43
标识
DOI:10.1038/s41590-023-01636-5
摘要
Abstract The malate shuttle is traditionally understood to maintain NAD+/NADH balance between the cytosol and mitochondria. Whether the malate shuttle has additional functions is unclear. Here we show that chronic viral infections induce CD8+ T cell expression of GOT1, a central enzyme in the malate shuttle. Got1 deficiency decreased the NAD+/NADH ratio and limited antiviral CD8+ T cell responses to chronic infection; however, increasing the NAD+/NADH ratio did not restore T cell responses. Got1 deficiency reduced the production of the ammonia scavenger 2-ketoglutarate (2-KG) from glutaminolysis and led to a toxic accumulation of ammonia in CD8+ T cells. Supplementation with 2-KG assimilated and detoxified ammonia in Got1-deficient T cells and restored antiviral responses. These data indicate that the major function of the malate shuttle in CD8+ T cells is not to maintain the NAD+/NADH balance but rather to detoxify ammonia and enable sustainable ammonia-neutral glutamine catabolism in CD8+ T cells during chronic infection.
科研通智能强力驱动
Strongly Powered by AbleSci AI