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. 2021 Feb 5;12:111. doi: 10.1186/s13287-020-02091-x

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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. 3 — KDM6B is a target gene of miR-22-3p derived from ASC-EVs. a Specific binding site of KDM6B and miR-22-3p predicted by an online website. b Dual-luciferase reporter gene assay of KDM6B and miR-22-3p. c RT-qPCR analysis of miR-22-3p expression in neurons upon transfection of miR-22-3p mimic or inhibitor. d RT-qPCR analysis of KDM6B expression in neurons upon transfection of miR-22-3p mimic or inhibitor. e Western blot analysis of KDM6B expression in neurons upon transfection of miR-22-3p mimic or inhibitor. f RT-qPCR analysis of miR-22-3p expression in neurons upon treatment of ASC-EVs. g RT-qPCR of KDM6B expression in neurons upon treatment of ASC-EVs. h Western blot analysis of KDM6B expression in neurons upon treatment of ASC-EVs. *p < 0.05, **p < 0.01, and ***p < 0.001. Measurement data were presented as mean ± standard deviation. The data among multiple groups were analyzed by ANOVA