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. 2019 Dec 20;4:23. doi: 10.1038/s41536-019-0085-4

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© The Author(s) 2019

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. 7 — EdU detection of proliferating cells in tamoxifen-labeled controls and injured ScxCreERT2/RosaT/ScxGFP mice was performed 2 hrs prior to sac at 2 hrs, d3, and d14 following herniation injury a. In uninjured controls, most proliferating cells (~60–70%) are Scx-lin cells (EdU+/Scx-lin). With injury, the percentage of non Scx-lin proliferating cells is increased at 2 hrs and d3 b, c, e, f, and is restored compared to control levels at d14 d, g. Error bars = SD. Scale = 100 μm.