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. 2016 Nov 21;17:944. doi: 10.1186/s12864-016-3230-0

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© The Author(s). 2016

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 — Characterization of MSCs following the ISCT criteria. a Microscope photographs of human stromal cells in culture taken at passage three: phase contrast micrographs seen at 4× and 10×. b-c Analysis of population doubling times: b boxplot of the doubling time distributions per stromal cell culture; c Wilcoxon test results of contrasted doubling times between stromal types. (DT = Doubling Time; W = Wilcoxon Test; CI = Confidence Interval). Labels for stromal cell types: AD = Adipose tissue MSC; BM = Bone marrow MSC; PL = Placental MSC; FIB = Dermal fibroblasts. **Significant p-values under 0.05. d-e Boxplots of normalized scatter intensities collected from flow-cytometry immunophenotyping assays using 10 different markers: CD105, HLADR, CD19, CD45, CD166, CD14, CD73, CD90, CD44 and CD34. (SSC = side scatter; FSC = forward scatter)