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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. 4 — High KDM6B expression exacerbates cerebral ischemic injury. a RT-qPCR analysis of KDM6B expression in neurons upon treatment of OE-KDM6B or si-KDM6B. b Western blot analysis determining transfection effect of OE-KDM6B, siRNA1, siRNA2, siRNA3, and their corresponding controls. c CCK-8 assay detection of viability of neurons after treatment with OE-KDM6B or si-KDM6B, or controls. d Flow cytometry detection of apoptosis after treatment of OE-KDM6B and si-KDM6B, or controls. e Western blot analysis of cleaved caspase 3, caspase 3, Bax, and Bcl-2 protein expression after treatment of OE-KDM6B or si-KDM6B, or controls, and the corresponding quantification. *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