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. 2021 Mar 12;18:70. doi: 10.1186/s12974-021-02120-3

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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. 2 — Microglia from aged female stroke patients express more KDM5C and KDM6A than male ischemic microglia. Representative immunohistochemistry microphotographs depicting KDM5C/KDM6A and Iba-1 staining of postmortem human brain tissue from acute ischemic stroke subjects and age-matched control (> 60 years). a, c 20X and 40X fields (boxed areas in 20X images) demonstrate the co-localization of KDM5C/KDM6A and Iba-1in microglia; scale bar = 25 μm and 50 μm, respectively. b, d Quantification of the ratios of KDM5C⁺/KDM6A⁺&Iba-1⁺ cells over total Iba-1⁺ cells (N = 6 control and 6 stroke subjects/group). *P<0.05