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. 2022 Mar 21;13(3):254. doi: 10.1038/s41419-022-04529-x

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© The Author(s) 2022

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. 7 — Increase Smad1/5 in NRK-52E cells by transfection of Overexpression-Smad1/5(OE-Samd1/5) plasmid. Representative a Western blot and quantitative data were revealed the expression of b p-Smad1/5^(ser463/465), Smad1, Smad5, and d SnoN in NRK-52E cells under different conditions. c Graphical presentations show the relative abundance of SnoN mRNA after normalization with β-actin mRNA analysised by RT-qPCR. Representative e Western blot and f quantitative data were revealed the expression of E-cadherin, Collagen-III, and Vimentin in NRK-52E cells under different conditions, *P < 0.05 (n = 3). g The binding site between Smad1/5 and SKIL promoter predicted by Jaspar. h Luciferase detected the binding of Smad1/5 to SKIL promoter in HEK 293 T cells.