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. 2018 Apr 30;27(6):979–993. doi: 10.1177/0963689718761657

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© The Author(s) 2018

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Fig. 6. — Evaluation of the abilities of human multilineage-differentiating stress enduring (Muse) cells and human mesenchymal stem cells (MSCs) to migrate toward sera from intact and lung ischemia–reperfusion (IR) injury model rats. Migrated cells were counted in 10 random high-power fields (HPFs) at 400× magnification, and the averages were used for comparison. When intact rat serum was used, 1.30 ± 1.00 MSCs and 1.20 ± 0.98 Muse cells were counted per HPF. When serum from IR injury model rats was used, the corresponding values were 4.40 ± 1.80 cells/HPF and 46.50 ± 10.43 cells/HPF, respectively. Data are presented as means ± standard deviations. ***P < 0.001.