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. 2022 Jun 11;19:143. doi: 10.1186/s12974-022-02512-z

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© The Author(s) 2022

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. 2 — Treg improved the behavioral disorder of TMT-intoxicated mice. The MWM test was performed 10 days after Treg injection. Latency time (s) on a hidden platform (A) and time in quadrant (%) (B) were measured (n = 10–13 mice/group). The EPM test was performed 10 days after Treg injection. Number of closed arm entries (C) and number of open arm entries (D) were recorded (n = 10–13 mice/group). Error bars represent the mean ± SEM. Significance was determined by Tukey’s HSD test (*p < 0.05, ***p < 0.001 vs. the Con group and ^#p < 0.05, ^##p < 0.01, ^###p < 0.001 vs. the TMT group)