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. 2022 Jun 21;13:267. doi: 10.1186/s13287-022-02916-x

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© The Author(s) 2022

Open AccessThis 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 licence, and indicate if changes were made. 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/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Comparison of biological characteristics of CD146 +/− MSCs subpopulations. A Flow Cytometry detection for CD146 expression in UC-MSCs after separation using magnetic beads. B The cellular morphology of CD146 +/− subsets after separation using magnetic beads. C Flow Cytometry detection of surface markers of CD146 +/− MSCs subsets: CD105, CD73, and CD90 were positive, and CD45 and CD34 were negative. D CD146 +/− MSCs subsets were labeled with Dye eFluor™ 670, and cell proliferation was assayed by flow cytometry at 0 h, 24 h, 48 h and 72 h. E Cell proliferation index calculated based on flow experimental results