ATF4 Regulates CD4+ T Cell Immune Responses through Metabolic Reprogramming.

T cells are strongly regulated by oxidizing environments and amino acid restriction. How T cells reprogram metabolism to adapt to these extracellular stress situations is not well understood. Here, we show that oxidizing environments and amino acid starvation induce ATF4 in CD4⁺ T cells. We also demonstrate that Atf4 -deficient CD4⁺ T cells have defects in redox homeostasis, proliferation, differentiation, and cytokine production. We further reveal that ATF4 regulates a coordinated gene network that drives amino acid intake, mTORC1 activation, protein translation, and an anabolic program for de novo synthesis of amino acids and glutathione. ATF4 also promotes catabolic glycolysis and glutaminolysis and oxidative phosphorylation and thereby provides precursors and energy for anabolic pathways. ATF4-deficient mice mount reduced Th1 but elevated Th17 immune responses and develop more severe experimental allergic encephalomyelitis (EAE). Our study demonstrates that ATF4 is critical for CD4⁺ T cell-mediated immune responses through driving metabolic adaptation. • Oxidizing environments and amino acid starvation induce ATF4 in CD4⁺ T cells • ATF4 increases mTORC1 activation plus intake and de novo synthesis of amino acids • ATF4 enhances glycolysis, glutaminolysis, and oxidative phosphorylation • ATF4 deficiency leads to decreases in Th1 but increases in Th17 immune responses. Oxidizing environments and availability of extracellular amino acids are major mechanisms that regulate T cell proliferation and function. Yang et al. demonstrate that ATF4 drives metabolic reprogramming, which allows CD4⁺ T cells to adapt to these stresses. [ABSTRACT FROM AUTHOR]