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. 2018 Feb 6;4:9. doi: 10.1038/s41420-017-0001-x

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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. 1 — a Controlled (untreated) cells had cobblestone like morphology, whereas those treated with 5 ng/mL TGF-β1 for 48 h showed fibroblast-like morphology. Original magnification power = ×400. b, c Epithelial marker (ZO-1) was significantly decreased, whereas mesenchymal marker (vimentin) was significantly increased. GAPDH served as the protein loading control. Each bar represents mean ± SD of the data derived from three independent experiments. *p < 0.05 vs. control