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. 2021 Dec 4;12:593. doi: 10.1186/s13287-021-02654-6

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 7 — Assessment of the role of LUCAT1 in iPSC-ECs following e-cig treatment. A qPCR validation of LUCAT1 expression following knockdown with 25 µM siRNA for negative control (siNC) and for LUCAT1 (siLUCAT1). B Permeability, C ROS levels, and D, E representative images and corresponding quantitative data of migration assays were assessed in iPSC-ECs treated with either siNC, siLUCAT1, siNC + e-cig (6.5 TPE), or siLUCAT1 + e-cig (n = 3–4). Data are represented as mean ± SD, and * and ** indicate p < 0.05 and p < 0.001, respectively. Scale bars = 500 μm