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. 2022 Aug 10;29(8):831–840. doi: 10.1038/s41594-022-00814-7

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© The Author(s) 2022

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. 7 — Extended Data Figure 7. (a) Photomicrographs of glial fibrillary acid protein (GFAP) immunohistochemistry on consecutive sections depicted in Fig. 6c. Left column: holo-^hcY104A injections (6, 9 and 12 µg). Right column: holo-^hcY104A + rmPrP_23–231. GFAP immunoreaction was increased in areas of neuronal damage (white asterisks) and around needle tracts (white arrowheads). (b) Micrographs demonstrating an intensive GFAP immunoreaction in areas with extensive holo-POM1 (6 µg)- induced neurotoxicity. Left panel: POM1 injection (6 µg). Right panel: holo-^hcY104A + rmPrP_23–231. Sections are consecutive to those shown in Fig. 6f.