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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. 1 — Static lung elastance on days 1 and 3. Mice were subjected to cecal ligation and puncture (CLP). A sham-operated group was used as a control CLP. At day 1, some animals were euthanized after establishment of ARDS in order to evaluate static lung elastance (Est,L), while other 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 mean ± standard deviation 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 MSC-MICE group