Year: 2017
Type: article
Abstract: Significance Regulatory T cells (Tregs) play a critical role in maintaining immune tolerance to self-antigens and in suppressing excessive immune responses that may cause collateral damage to the host. Unlike other CD4 + T cells, Tregs have a distinct, yet-to-be-established metabolic machinery to produce energy for survival and function. Here we show that the metabolic sensor LKB1 is critical for the survival and function of Tregs through regulation of their cellular metabolism. Interestingly, AMP-activated protein kinase, the best-studied downstream kinase of LKB1, is largely dispensable for LKB1 function in Tregs; the MAP/microtubule affinity-regulating kinases and salt-inducible kinases may mediate its functions. We highlight LKB1 as metabolic regulator that links cellular metabolism to immune cell functions.
Language: English
Topic: T-cell and B-cell Immunology
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: hybrid
Funders: Howard Hughes Medical Institute, March of Dimes Foundation, Leona M. and Harry B. Helmsley Charitable Trust, Fondation Leducq, Ipsen, National Institutes of Health, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Environmental Health Sciences
Awards: G150763035, G1820179381, G2073198546, G2659625731, G303972377, G3246578927, G352318888, G352863456, G3812021946, G4093887802, G4229701413, Spatial Regulation of Developmental Gene Expression, G4542402193, G680976502, G9000030100, G9000055537, G9000105172, G9000241332, Cancer Center Support Grant (CCSG)
OpenAlex ID: W2767460177