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Merck

T Cell Activation Depends on Extracellular Alanine.

Cell reports (2019-09-19)
Noga Ron-Harel, Jonathan M Ghergurovich, Giulia Notarangelo, Martin W LaFleur, Yoshiki Tsubosaka, Arlene H Sharpe, Joshua D Rabinowitz, Marcia C Haigis
ABSTRACT

T cell stimulation is metabolically demanding. To exit quiescence, TĀ cells rely on environmental nutrients, including glucose and the amino acids glutamine, leucine, serine, and arginine. The expression of transporters for these nutrients is tightly regulated and required for TĀ cell activation. In contrast to these amino acids, which are essential or require multi-step biosynthesis, alanine can be made from pyruvate by a single transamination. Here, we show that extracellular alanine is nevertheless required for efficient exit from quiescence during naive TĀ cell activation and memory TĀ cell restimulation. Alanine deprivation leads to metabolic and functional impairments. Mechanistically, this vulnerability reflects the low expression of alanine aminotransferase, the enzyme required for interconverting pyruvate and alanine, whereas activated TĀ cells instead induce alanine transporters. Stable isotope tracing reveals that alanine is not catabolized but instead supports protein synthesis. Thus, TĀ cells depend on exogenous alanine for protein synthesis and normal activation.

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Sigma-Aldrich
Anti-Puromycin, clone 12D10, Alexa Fluorā„¢ 647 Conjugate Antibody, clone 12D10, 0.5 mg/mL, from mouse