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. 2015 Nov 26;6:230. doi: 10.1186/s13287-015-0226-7

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© Güldner et al. 2015

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. 3 — Lung inflammation on days 1 and 3. Lung tissue protein expressions of tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6, IL-10, vascular endothelial growth factor (VEGF), and platelet-derived growth factor (PDGF). Cecal ligation and puncture (CLP) animals were randomized to receive saline or non-expanded endothelial progenitor cells (EPC-NEXP), expanded endothelial progenitor cells (EPC-EXP), human mesenchymal stem cells (MSC-HUMAN), or mouse mesenchymal stem cells (MSC-MICE), intravenously. Values expressed as a box-and-whiskers plot of eight animals in each group. *P < 0.05, versus respective sham group. **P < 0.05, versus CLP group at day 3. ^# P < 0.05, versus EPC-NEXP group. ^## P < 0.05, versus EPC-EXP group. ^† P < 0.05, versus MSC-HUMAN group