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. 2023 Oct 28;14(10):706. doi: 10.1038/s41419-023-06228-7

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — A Single-cell analysis showing the expression of various adenosine receptors in CD45⁺ cells isolated from TA muscles of wild-type mice at day 4 post-CTX injury. 1. Resolution-related MΦs, 2. Growth factor-expressing MΦs, 3. Pro-inflammatory MΦs, 4. Antigen-presenting MΦs. 5. Neutrophils, 6. CD8a⁺ Clec9a⁺dendritic cells, 7. Fibroblasts, 8. Fibroblast-like cells, 9. Myeloid CD8a^- dendritic cells, 10. Endothelial cells, 11. T cells, NK-T cells, 12. Lymphoid CD8a⁺ dendritic cells. B mRNA expressions of various adenosine receptors and inflammatory markers in muscle-derived CD45⁺ cells isolated at various time points post-CTX injury detected by RT-qPCR. Data are expressed as mean and individual values and statistical significance was determined by two-tailed Student’s t-test and ANOVA. *p < 0.05, **p < 0.01 (n = 4).