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. 2019 May 27;20:32. doi: 10.1186/s40360-019-0312-z

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© The Author(s). 2019

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. 6 — DEX does not affect stem Leydig cell proliferation. Panel a-c: EDU-labeled stem Leydig cells (green color, white arrow) afte treatment in the BM for 5 days. Panel: (a) Control; (b) DEX 100 nM; (c) EDU-labeled stem Leydig cell numbers (n = 6). Panel D: Medium testosterone (T) levels after seminiferous tubules were treated with various concentrations of DEX (0–100 nM) in the BM for 7 days and then these tubules were switched to the LIM for additional 14 days (n = 4–8). In Panel c and d, the data were presented as the mean ± SEM and there was no significant difference when compared to control group at P < 0.05