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. 2021 Jul 8;14:358. doi: 10.1186/s13071-021-04865-5

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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. 2 — p38 MAPK, ERK and Akt signaling pathway activation in response to GEV stimulation of mouse macrophages. a GEVs were inoculated into mouse macrophages, and cells were collected at the indicated time points for measurement of total protein and phosphorylated protein expression using western blotting. b Gray value analysis of phospho-p38/β-actin. c Gray value analysis of phospho-ERK/β-actin. d Gray value analysis of phospho-AKT/β-actin. The results are shown as the mean ± SEM of triplicate experiments. Significant differences vs 0-h control: *p < 0.05, **p < 0.01, ***p < 0.001