UCLA

T cell activation stimulates substantially increased protein synthesis activity to accumulate sufficient biomass for cell proliferation. The protein synthesis is fueled by the amino acids transported from the environment. Steroid nuclear receptor coactivator 2 (SRC2) is a member of a family of transcription coactivators. Here, we show that SRC2 recruited by c-Myc enhances CD4⁺ T cell activation to stimulate immune responses via upregulation of amino acid transporter Slc7a5. Mice deficient of SRC2 in T cells (SRC2^fl/fl/CD4^Cre) are resistant to the induction of experimental autoimmune encephalomyelitis (EAE) and susceptible to Citrobacter rodentium (C. rodentium) infection. Adoptive transfer of naive CD4⁺ T cells from SRC2^fl/fl/CD4^Cre mice fails to elicit EAE and colitis in Rag1^/ recipients. Further, CD4⁺ T cells from SRC2^fl/fl/CD4^Cre mice display defective T cell proliferation, cytokine production, and differentiation both in vitro and in vivo. Mechanically, SRC2 functions as a coactivator to work together with c-Myc to stimulate the expression of amino acid transporter Slc7a5 required for T cell activation. Slc7a5 fails to be up-regulated in CD4⁺ T cells from SRC2^fl/fl/CD4^Cre mice, and forced expression of Slc7a5 rescues proliferation, cytokine production, and the ability of SRC2^fl/fl/CD4^Cre CD4⁺ T cells to induce EAE. Therefore, SRC2 is essential for CD4⁺ T cell activation and, thus, a potential drug target for controlling CD4⁺ T cell-mediated autoimmunity.