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. 2018 Apr 11;9:100. doi: 10.1186/s13287-018-0818-0

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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 morphological change (a), reactive oxygen species (ROS) staining (b), and quantification (c) of RAW264.7 cells in the control group (Lap 0 μg/mL) and Lap (12.5, 50, 100 μg/mL) groups. ELISA assay (d), and mRNA expression (e) of the proinflammatory (tumor necrosis factor alpha (TNF-α), interferon-gamma (IFN-γ), interleukin (IL)-6, IL-1β) and anti- inflammatory (IL-1α, IL-10, arginase 1 (Arg-1)) cytokines from RAW264.7 cells in the control and Lap groups. The experiment was repeated three times with similar results. *P < 0.05, **P < 0.01, ***P < 0.001