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. 2019 Oct 17;10:301. doi: 10.1186/s13287-019-1405-8

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© The Author(s). 2019

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. 7 — CP-MSCs show greater ability to regulate macrophage from M1 to M2. a–c Flow cytometry analysis of macrophage polarization, M1 polarization marker (CD86), M2 polarization marker (CD163). d, e The concentration of TNF-a and IL-10 in the cell culture supernatant. f–m The expression of major M1 markers (IL-1β, TNF-α, iNOS, and IL-6) and M2 markers (IL-10, Arg-1, CD163, and CD206). All data are expressed as the means ± SD (N = 3; *p < 0.05, **p < 0.01, ***p < 0.001, NS, no significant)