| Literature DB >> 32023446 |
Dominic G Roy1, Jocelyn Chen1, Victoria Mamane2, Eric H Ma3, Brejnev M Muhire4, Ryan D Sheldon4, Tatiana Shorstova5, Rutger Koning6, Radia M Johnson7, Ekaterina Esaulova8, Kelsey S Williams4, Sebastian Hayes9, Mya Steadman9, Bozena Samborska1, Amanda Swain8, Audrey Daigneault6, Victor Chubukov9, Thomas P Roddy9, William Foulkes10, J Andrew Pospisilik11, Marie-Claude Bourgeois-Daigneault12, Maxim N Artyomov8, Michael Witcher5, Connie M Krawczyk13, Catherine Larochelle2, Russell G Jones14.
Abstract
Epigenetic modifications on DNA and histones regulate gene expression by modulating chromatin accessibility to transcription machinery. Here we identify methionine as a key nutrient affecting epigenetic reprogramming in CD4+ T helper (Th) cells. Using metabolomics, we showed that methionine is rapidly taken up by activated T cells and serves as the major substrate for biosynthesis of the universal methyl donor S-adenosyl-L-methionine (SAM). Methionine was required to maintain intracellular SAM pools in T cells. Methionine restriction reduced histone H3K4 methylation (H3K4me3) at the promoter regions of key genes involved in Th17 cell proliferation and cytokine production. Applied to the mouse model of multiple sclerosis (experimental autoimmune encephalomyelitis), dietary methionine restriction reduced the expansion of pathogenic Th17 cells in vivo, leading to reduced T cell-mediated neuroinflammation and disease onset. Our data identify methionine as a key nutritional factor shaping Th cell proliferation and function in part through regulation of histone methylation.Entities:
Keywords: EAE; SAM; T cells; Th17 cells; histone methylation; inflammation; metabolism; methionine
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Year: 2020 PMID: 32023446 DOI: 10.1016/j.cmet.2020.01.006
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287