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. 2026 Apr 23;17:5648. doi: 10.1038/s41467-026-72203-3

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© The Author(s) 2026

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Fig. 3 — a Wound healing and transwell assays were used to evaluate CD34⁺ cells’ migration ability. b Quantitative data of the wound healing and transwell. Data in (b) are from n = 5 biologically independent samples. c Adhesion assays of the CD34⁺ cells. d Quantitative data for the adhesion assays. Data in (d) are from n = 5 biologically independent samples. e Tube formation assay of the CD34⁺ cells. f Tube formation was quantified by total tube formation length and branch junction. Data in (f) are from n = 5 biologically independent samples. All data are presented as mean ± s.d. Statistical significance and P-values were analyzed by using one-way ANOVA followed by Tukey’s multiple comparisons test (two-sided). *P < 0.05, **P < 0.01, ***P < 0.001. Scale bars, 200 μm (a); 100 μm (c); 200 μm (e). Source data are provided as a Source Data file.