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. 2016 Jul 8;7:2041731416656148. doi: 10.1177/2041731416656148

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© The Author(s) 2016

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) 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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Figure 4. — In vitro angiogenic potential of MAPC and MSC. (a–d) ELISA analysis using conditioned media from MAPC and MSC in control conditions; (a) ELISA analysis of interleukin 8 (IL-8) secretion in MAPC versus MSC, (b) GRO-α secretion in MAPC versus MSC, and (c) VEGF secretion in MAPC versus MSC. (d) CXCL-5 secretion in MAPC versus MSC. CXCL-5 was below detectable limits of the assay for MSC (n = 3 for each, *p < 0.01). (e) Matrigel tube formation assay with human umbilical vein endothelial cells (HUVEC) exposed to MAPC and MSC conditioned media, n = 3, 6-h time point.