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. 2021 Jun 29;12:370. doi: 10.1186/s13287-021-02439-x

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 6 — Mel-ADMSCs therapy preserved the integrity of alpha-microtubule and suppression of cellular expression of CD68 in testis by 72 h after IR procedure. A–E Illustrating the microscopic finding (× 400) of immunohistochemical stain for identification of the expression of alpha-microtubule (α-MT) (spindle shape, gray color). F Analytical result of number of α-MT, * vs. other groups with different symbols (†, ‡, §), p < 0.0001. G–K Illustrating the immunofluorescent (IF) microscopic finding (× 400) for identification of CD68-positively stained cells (green color). L Analytical result of number of CD68+ cells, * vs. other groups with different symbols (†, ‡, §), p < 0.0001. HPF, high-power field. All statistical analyses were performed by one-way ANOVA, followed by Bonferroni multiple comparison post hoc test (n = 6 for each group). Symbols (*, †, ‡, §) indicate significance (at 0.05 level)