| Literature DB >> 27411012 |
Noga Ron-Harel1, Daniel Santos2, Jonathan M Ghergurovich3, Peter T Sage4, Anita Reddy1, Scott B Lovitch4, Noah Dephoure1, F Kyle Satterstrom1, Michal Sheffer5, Jessica B Spinelli1, Steven Gygi1, Joshua D Rabinowitz6, Arlene H Sharpe4, Marcia C Haigis7.
Abstract
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.Entities:
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Year: 2016 PMID: 27411012 PMCID: PMC5330619 DOI: 10.1016/j.cmet.2016.06.007
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287