Metabolic control of innate lymphoid cells in health and disease

被引:18
作者
Zhou, Lei [1 ]
Lin, Qingxia [1 ]
Sonnenberg, Gregory F. [2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Immune Therapy Inst, Renji Hosp, Sch Med, Shanghai, Peoples R China
[2] Cornell Univ, Joan & Sanford I Weill Dept Med, Div Gastroenterol & Hepatol, Dept Microbiol & Immunol, New York, NY 10021 USA
[3] Cornell Univ, Jill Roberts Inst Res Inflammatory Bowel Dis, Weill Cornell Med, New York, NY 10021 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
ARYL-HYDROCARBON RECEPTOR; ALTERNATIVELY ACTIVATED MACROPHAGES; T-CELL; TYPE-2; CYTOKINES; IMMUNITY; OBESITY; DRIVES; IL-22; CATECHOLAMINES;
D O I
10.1038/s42255-022-00685-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Innate lymphoid cells (ILCs) are an integral part of the innate immune system. This Review discusses how ILC function is regulated by both intrinsic and extrinsic metabolic pathways, and how ILCs contribute to metabolic disease. Innate lymphoid cells (ILCs) are a family of predominantly tissue-resident lymphocytes that critically orchestrate immunity, inflammation, tolerance and repair at barrier surfaces of the mammalian body. Heterogeneity among ILC subsets is comparable to that of adaptive CD4(+) T helper cell counterparts, and emerging studies demonstrate that ILC biology is also dictated by cellular metabolism that adapts bioenergetic requirements during activation, proliferation or cytokine production. Accumulating evidence in mouse models and human samples indicates that ILCs exhibit profound roles in shaping states of metabolic health and disease. Here we summarize and discuss our current knowledge of the cell-intrinsic and cell-extrinsic metabolic factors controlling ILC responses, as well as highlight contributions of ILCs to organismal metabolism. It is expected that continued research in this area will advance our understanding of how to manipulate ILCs or their metabolism for therapeutic strategies that benefit human health.
引用
收藏
页码:1650 / 1659
页数:10
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