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. 2024 Oct 16;14:24275. doi: 10.1038/s41598-024-75517-8

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 3 — Identification of exosomes in the sham surgery group and model group by (A) transmission electron microscopy, (B) particle size analysis, (C) fluorescence analysis of the exosome markers CD9 and CD81 and IgG control, and (D) western blot analysis of the exosome markers HSP70, TSG101, and CD9 in the sham and I/R groups. The blots cut prior to hybridization with antibodies and the original blots/gels were presented in supplementary Fig. 1. (n = 3 per group).