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. 2016 Sep 22;13:250. doi: 10.1186/s12974-016-0715-3

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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. 7 — Phagocytic activity of microglia does not change after treatment with teriflunomide. Flow cytometric histograms of unstimulated (a) and LPS-treated (b) microglia represent the mean fluorescence intensity which displays the amount of incorporated fluorescent latex beads (filled: 4 °C control; solid line: cells without teriflunomide; dotted line: cells with 5 μM teriflunomide). c, d Data are expressed as the ratio of untreated microglia in relation to teriflunomide-treated microglia. All data are given as mean ± SD of four independent experiments. For comparison to medium control, repeated measures ANOVA with Bonferroni’s multiple comparison t tests was used