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. 2019 Oct 10;10(10):775. doi: 10.1038/s41419-019-2005-3

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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. 2 — hESCs were treated with artificial decidua element (10 nM E₂, 1 μM MPA, 0.5 mM cAMP) or VEGF for 72 h. a, b Real-time PCR (a) and western blot (b) analyses of poFUT1, CD31, and VE-cadherin expression. c Immunofluorescent staining of poFUT1, CD31, and VE-cadherin in hESCs. d Tube formation assay of hESC angiogenesis. Significance was indicated by *P < 0.05, **P < 0.01, ***P < 0.001