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. 2017 Feb 7;25(2):345-357.
doi: 10.1016/j.cmet.2016.12.011. Epub 2017 Jan 19.

Serine Is an Essential Metabolite for Effector T Cell Expansion

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Free article

Serine Is an Essential Metabolite for Effector T Cell Expansion

Eric H Ma et al. Cell Metab. .
Free article

Erratum in

  • Serine Is an Essential Metabolite for Effector T Cell Expansion.
    Ma EH, Bantug G, Griss T, Condotta S, Johnson RM, Samborska B, Mainolfi N, Suri V, Guak H, Balmer ML, Verway MJ, Raissi TC, Tsui H, Boukhaled G, Henriques da Costa S, Frezza C, Krawczyk CM, Friedman A, Manfredi M, Richer MJ, Hess C, Jones RG. Ma EH, et al. Cell Metab. 2017 Feb 7;25(2):482. doi: 10.1016/j.cmet.2017.01.014. Cell Metab. 2017. PMID: 28178570 No abstract available.

Abstract

During immune challenge, T lymphocytes engage pathways of anabolic metabolism to support clonal expansion and the development of effector functions. Here we report a critical role for the non-essential amino acid serine in effector T cell responses. Upon activation, T cells upregulate enzymes of the serine, glycine, one-carbon (SGOC) metabolic network, and rapidly increase processing of serine into one-carbon metabolism. We show that extracellular serine is required for optimal T cell expansion even in glucose concentrations sufficient to support T cell activation, bioenergetics, and effector function. Restricting dietary serine impairs pathogen-driven expansion of T cells in vivo, without affecting overall immune cell homeostasis. Mechanistically, serine supplies glycine and one-carbon units for de novo nucleotide biosynthesis in proliferating T cells, and one-carbon units from formate can rescue T cells from serine deprivation. Our data implicate serine as a key immunometabolite that directly modulates adaptive immunity by controlling T cell proliferative capacity.

Keywords: Phgdh; Shmt; T cell; glycolysis; immunometabolism; immunotherapy; metabolic reprogramming; metabolism; serine; serine biosynthesis.

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