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. 2020 Dec 12;11(12):1054. doi: 10.1038/s41419-020-03230-1

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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 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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Fig. 3 — A Paraffin sections of wound tissue from Plg-R_KT^−/− and Plg-R_KT^+/+ littermates were immunostained with anti-Plg-R_KT mAB (red) and DAPI (blue). Scale bar = 200 µm. White arrows indicate hair follicles, white arrowheads show keratinocytes. B Quantitation of the Plg-R_KT staining in Plg-R_KT^+/+ (shown as % of total wound area). By Krustal–Wallis test, p = 0.054, Krustal–Wallis statistic = 7.1 followed by Dunns Multiple Comparisons, Day 0 vs. Day 4, p ≥ 0.999, Day 0 vs. Day 11 p = 0.040 and Day 0 vs. Day 20, p = 0.404, (n = 4). Medians are displayed. Images were captured with a Zeiss Axio Imager Z1 (Zeiss, Oberkochen, Germany) or Nikon A1R Eclipse Ti-E inverted microscope (Nikon Instruments, Amsterdam, Netherlands). Quantification of fluorescent areas was performed using Image J software.