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. 2021 Aug 9;12:448. doi: 10.1186/s13287-021-02530-3

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© The Author(s) 2021

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 — Cell proliferation and migration under normoxic and hypoxic conditions. A The number of mouse primary myoblasts (mPM), human bone marrow-derived mesenchymal stromal cells (hMSC), pig bone marrow-derived mesenchymal stromal cells (pMSC), cells in co-cultures of hMSC and mPM, and cells in co-cultures of pMSC and mPM, cultured in two types of medium: MSCmed and PMmed, under normoxic (NORM) or hypoxic (HYPO) conditions. B The invaded area measured in scratch wound healing assay of hMSC and pMSC cultured in MSCmed under normoxic and hypoxic conditions. C The scratch wound healing assay of hMSC and pMSC cultured in MSCmed under normoxic and hypoxic conditions. P value: *< 0.05; **< 0.01; ***< 0.001; ****< 0.0001