Naive T cell stimulation activates anabolic metabolism to fuel the transition from quiescence to growth and proliferation. Here we show that naive CD4(+) T cell activation induces a unique program of mitochondrial biogenesis and remodeling. Using mass spectrometry, we quantified protein dynamics during T cell activation. We identified substantial remodeling of the mitochondrial proteome over the first 24 hr of T cell activation to generate mitochondria with a distinct metabolic signature, with one-carbon metabolism as the most induced pathway. Salvage pathways and mitochondrial one-carbon metabolism, fed by serine, contribute to purine and thymidine synthesis to enable T cell proliferation and survival. Genetic inhibition of the mitochondrial serine catabolic enzyme SHMT2 impaired T cell survival in culture and antigen-specific T cell abundance in vivo. Thus, during T cell activation, mitochondrial proteome remodeling generates specialized mitochondria with enhanced one-carbon metabolism that is critical for T cell activation and survival.
Mitochondrial Biogenesis and Proteome Remodeling Promote One-Carbon Metabolism for T Cell Activation.
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作者:Ron-Harel Noga, Santos Daniel, Ghergurovich Jonathan M, Sage Peter T, Reddy Anita, Lovitch Scott B, Dephoure Noah, Satterstrom F Kyle, Sheffer Michal, Spinelli Jessica B, Gygi Steven, Rabinowitz Joshua D, Sharpe Arlene H, Haigis Marcia C
| 期刊: | Cell Metabolism | 影响因子: | 30.900 |
| 时间: | 2016 | 起止号: | 2016 Jul 12; 24(1):104-17 |
| doi: | 10.1016/j.cmet.2016.06.007 | ||
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