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. 2017 Jun 15;8:146. doi: 10.1186/s13287-017-0599-x

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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. 2 — Expression of miR-223 was upregulated in renal tubular epithelial cells (RTECs) cocultured with mesenchymal stem cells (MSCs) or hypoxia-pretreated MSCs (htMSCs). RTECs were treated with hypoxia/reoxygenation (HR) stimulation and then cocultured with MSCs or htMSCs in a double-chamber. Cells were harvested at 48 h. a Expression of miR-223 in RTECs was detected by qRT-PCR. ^a P < 0.05, versus the RTEC group; ^b P < 0.05, versus the HR RTEC group. b Expression of miR-223 in MSCs was detected by qRT-PCR. ^a P < 0.05, versus the normal cultured MSCs