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Cited by 331

The DOI matches its Crossref record; 86 of the 86 references it cites were found in a registry or an index.

Inosine is an alternative carbon source for CD8+-T-cell function under glucose restriction

Open access
Wang, Tingting, Gnanaprakasam, J. N. Rashida, Chen, Xuyong, Kang, Siwen, Xu, Xuequn, Sun, Hua, Liu, Lingling, Rodgers, Hayley, Miller, Ethan, Cassel, Teresa A., Sun, Qiushi, Vicente-Muñoz, Sara, Warmoes, Marc O., Lin, Penghui, Piedra-Quintero, Zayda Lizbeth, Guerau-de-Arellano, Mireia, Cassady, Kevin A., Zheng, Song Guo, Yang, Jun, Lane, Andrew N., Song, Xiaotong, Fan, Teresa W.-M., Wang, Ruoning·2020·Nature Metabolism

Abstract

T cells undergo metabolic rewiring to meet their bioenergetic, biosynthetic and redox demands following antigen stimulation. To fulfil these needs, effector T cells must adapt to fluctuations in environmental nutrient levels at sites of infection and inflammation. Here, we show that effector T cells can utilize inosine, as an alternative substrate, to support cell growth and function in the absence of glucose in vitro. T cells metabolize inosine into hypoxanthine and phosphorylated ribose by purine nucleoside phosphorylase. We demonstrate that the ribose subunit of inosine can enter into central metabolic pathways to provide ATP and biosynthetic precursors, and that cancer cells display diverse capacities to utilize inosine as a carbon source. Moreover, the supplementation with inosine enhances the anti-tumour efficacy of immune checkpoint blockade and adoptive T-cell transfer in solid tumours that are defective in metabolizing inosine, reflecting the capability of inosine to relieve tumour-imposed metabolic restrictions on T cells.

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Metadata

Authors
Wang, T., Gnanaprakasam, J. N. R., Chen, X., Kang, S., Xu, X., Sun, H., Liu, L., Rodgers, H., Miller, E., Cassel, T. A., Sun, Q., Vicente-Muñoz, S., Warmoes, M. O., Lin, P., Piedra-Quintero, Z. L., Guerau-de-Arellano, M., Cassady, K. A., Zheng, S. G., Yang, J., Lane, A. N., Song, X., Fan, T. W.-M., & Wang, R.
Venue
Nature Metabolism
Published
2020-06-15
Volume
2
Issue
7
Pages
635-647
ISSN
2522-5812 (ISSN-L)
OpenAlex
W3034524707
Cited by
331
References
86
FWCI
9.40
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Inosine is an alternative carbon source for CD8+-T-cell function under glucose restriction. https://app.cochat.ai/papers/10.1038/s42255-020-0219-4
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Wang, T., Gnanaprakasam, J. N. R., Chen, X., Kang, S., Xu, X., Sun, H., Liu, L., Rodgers, H., Miller, E., Cassel, T. A., Sun, Q., Vicente-Muñoz, S., Warmoes, M. O., Lin, P., Piedra-Quintero, Z. L., Guerau-de-Arellano, M., Cassady, K. A., Zheng, S. G., Yang, J., . . . Wang, R. (2020). Inosine is an alternative carbon source for CD8+-T-cell function under glucose restriction. Nature Metabolism. https://doi.org/10.1038/s42255-020-0219-4

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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