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. 2023 May 11;26(6):1008–1020. doi: 10.1038/s41593-023-01326-3

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© The Author(s) 2023

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 2 — a, Arg1-YFP-positive microglia in male YARG mice, as recognised by α-GFP and α-ARG1 antibodies (representative image from 3 female animals). b, Arg1+microglia (arrows) and Arg1-negative-microglia (arrowheads) during mouse brain development. c, Arg1+microglia in BF/vStr at P10, P28 and P100 (representative images from 3 female animals per group). Each white dot represents a single Arg1+microglia and has been manually annotated. Scale bars, x = 50 μm, z = 10 μm (a), x = 10 μm (b), x = 1000 μm, z = 4 μm (c). Yellow squares indicate location of the corresponding images on their left; grey lines indicate the BF/vStr region.