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. 2024 Feb 5;56(2):408–421. doi: 10.1038/s12276-024-01168-4

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© The Author(s) 2024

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. 8 — a HE and SO staining of CCR2^fl/flLyz2-cre and WT mouse IVD tissue. b Immunofluorescence images and quantitative analysis of F4/80⁺/CCR2⁺, F4/80⁺/Cox2⁺ and F4/80⁺/CD206⁺ double-positive cells in the IVD tissue of CCR2^fl/flLyz2-cre and WT mice. Experiments were performed 5 times independently, and the data are presented as the means ± SDs. *p < 0.05; **p < 0.01; ***p < 0.001; ns: not significant, ANOVA.