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. 2020 Apr 28;17:137. doi: 10.1186/s12974-020-01815-3

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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. 3 — CSF1R KD resulted in a significant reduction of both residential microglia and macrophages. We gated for CD11b+/CD45+ cells indicative of both microglia and macrophages as depicted in a and b. c Three weeks post-stroke diabetic animals had an increase in residential microglia that CSF1R KD drastically lowered by 94%. d The macrophage infiltration after stroke was also lowered by 74% (N = 3–7/group)