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. 2017 May 12;8:112. doi: 10.1186/s13287-017-0565-7

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© The Author(s). 2017

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. 5 — BMSCs preconditioned with TMP enhances BMSCs homing into the ischemic brain region. a BMSCs that were labeled by BrdU (red) and nuclei labeled with DAPI (blue) were observed at the lesion site after MCAO. b Quantification of migrated BMSCs. Bars, 100 μm. Values are mean ± SD. *P < 0.01 vs. BMSCs. #P < 0.01 vs. TMP. BMSCs bone marrow-derived mesenchymal stem cells, TMP tetramethylpyrazine, MCAO middle cerebral artery occlusion, BrdU 5-bromo-2-deoxyuridine, DAPI 4′,6-diamidino-2-phenylindole (Color figure online)