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. 2022 Jul 26;13:359. doi: 10.1186/s13287-022-03018-4

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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. 6 — miR-152-5p/ATG14-mediated autophagy regulated osteogenic differentiation by reducing the elevated ROS. a ROS detection of sham and OVX’ MMSCs-M. Scar bar = 50um. b H₂O₂ (100um) was applied to OVX MMSCs-M in order to increase the ROS level. ROS detection of different groups in inhibitor NC + siNC, inhibitor NC + siNC + H₂O₂ (100uM), miR-152-5p inhibitor + siNC, miR-152-5p inhibitor + siNC + H₂O₂ (100uM), miR-152-5p inhibitor + siATG14 + H₂O₂. c Western blotting assays were performed to verify that ATG14-mediated autophagy regulated osteogenic differentiation by reducing the elevated ROS (n = 3). Scar bar = 50um. Data were shown as mean SD (p < 0.05*, p < 0.01**, p < 0.0005***, p < 0.0001****)