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. 2020 Apr 1;17:97. doi: 10.1186/s12974-020-01774-9

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© The Author(s) 2020

Open Access This 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 — Differential gene expression between adult and aging microglia. a–d Upregulated and downregulated genes, determined using DESeq2 analysis, between mature-adult mice (2 months) and aging mice (4 months, 6 months, 9 months, 12 months); adjusted p < 0.05, |log₂ fold-change| > 0.5. a Venn diagram showing upregulated genes in microglia. b Heatmap of top 15 genes upregulated in microglia. c Venn diagram showing downregulated genes in microglia. d Heatmap of top 15 genes downregulated in microglia. e and f STEM analysis of upregulated genes (e) and downregulated genes (f) in microglia during aging