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. 2018 Jul 13;9:2704. doi: 10.1038/s41467-018-05039-1

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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. 5 — Hhex-IRES-Venus is expressed by vascular endothelial cells and lymphatic endothelial cells during mouse development and adulthood. a–d Maximum intensity projections of confocal images of an E10.5 Hhex-IRES-Venus embryo in the CV region after Venus (white), PROX1 (green), and PECAM (red) immunostaining. e–l Maximum intensity projections of confocal images of an Hhex-IRES-Venus adult mouse small intestine (e–h) and skin (i–l) after Venus (white), LYVE1 (blue) and PECAM (red) immunostaining. Hhex-IRES-Venus expression is observed in blood endothelial cells (red arrowheads) as well as LECs (white arrowheads). Scale bars: 50 μm