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. 2018 Mar 7;19:41. doi: 10.1186/s12931-018-0740-0

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 4 — The TGFβ-induced EMT was affected by DPYSL3. a Decreased DPYSL3 induced the up-regulation of EMT. The LLC cells were treated with TGFβ (2 ng /mL) for 48 h. b The expression of EMT markers, TWIST1 and N-cadherin, increased when DPYSL3 was inhibited. c The RhoA activity also increased with the knockdown of DPYSL3