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. 2020 Jun 16;11:237. doi: 10.1186/s13287-020-01763-y

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© The Author(s) 2020

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. 5 — Antioxidant preconditioning promotes the cell survival of ADSCs in vitro. a Cell viability of ADSCs with or without antioxidant pretreatment in H₂O₂-induced cell injury model (n = 5 per group; **p < 0.01; ***p < 0.001). b Representative images of cell morphology of ADSCs treated with H₂O₂ (scale bar, 50 μm). c Cell apoptosis was evaluated by flow cytometry. d Western blotting of Bcl-2, Bax, and Cyclin-D1 in ADSCs treated with H₂O₂. e Relative expression of Bcl-2, Bax, and Cyclin-D1 in ADSCs treated with H₂O₂ (n = 3 per group; *p < 0.05; **p < 0.01). ADSCs, adipose tissue-derived mesenchymal stem cells; G-ADSCs, ADSCs pretreated with reduced glutathione; M-ADSCs, ADSCs pretreated with melatonin; H₂O₂, hydrogen peroxide