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. 2018 Jul 19;50(7):1–13. doi: 10.1038/s12276-018-0118-x

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© The Author(s) 2018

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. 2 — Myeloid cells are recruited to the liver post-thermal injury. a, b Flow cytometry shows an increase in EYFP+ and cd11b+ cells. c Immunofluorescence of Lysz-Cre ROSA-EYFP livers shows an enrichment of EYFP+ cells post-thermal injury, in particular around PVs. scale bar 100 μm. d Immunohistochemistry staining for F4/80+ cells show an increase post-thermal injury in these cells in the liver and surrounding PV sites; n = 5 for all the panels, scale bar 100 μm. *P < 0.05, and ***P < 0.001