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. 2016 Dec 30;7:189. doi: 10.1186/s13287-016-0448-3

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© The Author(s). 2016

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. 2 — pMSCs proliferation and viability. a Experimental schedule. BM basal medium. b Untreated pMSCs, pMSCs pretreated with 1 ug/mL of LL-37 (1 LL37_pre) or with 10 ug/mL of LL-37 (10 LL37_pre), and pMSCs treated with 1 ug/mL LL-37 (1 LL37_1d) or with 10 ug/mL of LL-37 (10 LL37_1d) were cultured for 7 days, then cell proliferation/viability was assessed by MTT. There was no difference of proliferation/viability among groups. Values represent the means ± SEM. Three independent experiments (biological replicates) were performed. LL-37 cathelicidin LL-3. pMSCs human placenta-derived MSCs