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. 2021 Sep 14;19:93. doi: 10.1186/s12964-021-00768-1

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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 — MB49-derived exosomes activate PTEN/AKT/STAT3/6 signaling pathways in BMDM. A BMDM were treated with MB49-derived exosomes for indicated time points, and the expression of PTEN, p-PI3K, p-AKT, p-STAT3 and p-STAT6 was analyzed by Western blot. B BMDM were stimulated with miR-92b-3p mimic or miR-1231-5p mimic or each inhibitor with MB49-derived exosomes for 3 h, respectively. The expression of PTEN, p-PI3K, p-AKT, p-STAT3 and p-STAT6 were detected by Western blot. Actin were used as a loading control. The experiments were performed three times and the relative protein ratio were analyzed by image J software. One way ANOVA, Mean ± SD, *P < 0.05; **P < 0.01; ***P < 0.001