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. 2019 Mar 26;9:5170. doi: 10.1038/s41598-019-41590-7

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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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Microvascular centreline RBC velocity of lung (filled circles) and endometrium (x) transplants in dorsal skinfold chambers (mean and SEM; n = 10 endometrium grafts out of 7 mice and n = 34 lung grafts out of 15 mice). Note the increasing centreline RBC velocity over time of the lung vasculature within the 14 days of observation, which reached about 5 to 10-fold the value of endometrium. As mentioned in the text, the centreline RBC velocity has been difficult to assess due to technical reasons and may even be underestimated in lung tissue. Contrary to that, the centreline RBC velocity in endometrium reached its maximal value at 6 days and then remained stable over time.