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. 2020 Sep 29;17:60. doi: 10.1186/s12987-020-00219-y

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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. 1 — Density and diameter of MV are not significantly different in samples of parietal cortex from not, intermediate, and high ADNC subjects. Density (a) and diameter (b) of MV (identified by IF for alpha-smooth muscle actin as shown in insets of representative images in both a and b) in sections of parietal cortex in not ADNC, intermediate (Int) ADNC, and high ADNC. c MV density assays similar to those in a, but identifying MV by chromogenic IHC for endothelial cell PECAM (c, scatter plot with mean and SEM; inset, representative image) and vWF (d, scatter plot with mean and SEM; inset, representative image). These assays show no significant differences in MV density and diameter among the three groups. Inset scale bars are 20 µm (a, c, d) and 10 µm (b). Sample sizes (n) are indicated in “Results”