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. 2023 Jan 24;14:396. doi: 10.1038/s41467-023-35907-4

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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. 7 — a Representative image of CD206 and CD86 immunostaining in wound tissue on day 3 and 7. b Quantification of CD206⁺ area in the wound tissue (n = 12 biologically independent samples in each group). c Quantification of CD86⁺ area in the wound tissue ((n = 12 biologically independent samples in each group). d Cytokine levels in wound tissue on day 3 (n = 3 biologically independent samples in each group). e Representative images of CD206 and DAPI staining of RAW264.7. f Quantification of the fluorescence intensity of CD206 in RAW264.7 cells (n = 10 biologically independent cells in each group). For (b–d and f), two-tailed t test was used. Data are presented as mean values ± SEM. Scale bars, 100 μm (images in a), 50 μm (images in e), 25 μm (inset in e). Source data are provided as a Source data file.