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. 2018 Nov 22;8:17255. doi: 10.1038/s41598-018-35610-1

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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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Validation of RNA-Seq results using QPCR. Fifteen DEGs, including Bag3, Cryab, Gprasp2, Tigar, Vegfb, Bmp1, Crabp1, Kdelr3, Gadd45a, Hacd3, Rel, Sirt7, Apob, Dhcr7, and Nfam1 were selected for result validation using QPCR. General consistency in results was found between the two methods. *P < 0.05, fold change > 1.5. Analyses of at least 3 independent culture sets was performed for each gene and results displayed as mean ± SE. P < 0.05 is considered as statistically significant.