Abstract
We demonstrate that the mechanism of redox remodeling during mouse T-cell activation involves secretion of glutathione by dendritic cells and its subsequent cleavage to cysteine. Extracellular cysteine accumulation results in a lower redox potential, which is conducive to proliferation, and changes the net redox status of exofacial protein domains. Regulatory T cells inhibit this redox metabolite signaling pathway, which represents a previously unrecognized mechanism for immunosuppression of effector T cells.
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Acknowledgements
This work was supported in part by a grant from the US National Institutes of Health (DK64959 and NIH5P60 DK20572).
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All authors contributed to the experimental design, data analysis and manuscript writing. Z.Y. and S.K.G. performed the experiments.
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Yan, Z., Garg, S., Kipnis, J. et al. Extracellular redox modulation by regulatory T cells. Nat Chem Biol 5, 721–723 (2009). https://doi.org/10.1038/nchembio.212
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DOI: https://doi.org/10.1038/nchembio.212
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