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. 2019 Aug 14;9:11861. doi: 10.1038/s41598-019-47891-1

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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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ER-INP increases migratory capacity of HUVECs. HUVECs were co-cultured with transfected HEK293 cells (A–C) and RAW26.4 cells (D–F) for different lengths of time. Then, the migratory capacity of HUVECs was observed under a microscope (A,D) and analysed (B,C,E,F). The quantitative charts of scratch width (B,E). The quantitative charts of scratch closure rate (C,F). ER-INP increases the migratory capacity of HUVECs. Data represent the mean ± SD from 3 parallel experiments of representative data from multiple independent experiments (B,C,E,F).