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. 2022 Apr 11;28(2):91–103. doi: 10.1177/17534259221090679

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© The Author(s) 2022

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 7. — Measurement of M1-Mφ and M2-Mφ signature cytokines produced by Mox-LDL-treated M1-Mφs and M2-Mφs. (A) IL-6 (M1-φ marker) and (B) IL-10 (M2-φ marker) levels in the culture supernatants of M0-Mφs, M1-φs, M2-Mφs, and Mox-LDL-treated (at a concentration of 50 μg/ml for 24 h) M1-Mφs (Mox-LDL/M1-Mφs) and M2-Mφs (Mox-LDL/M2-Mφs) as measured by ELISA. Column bars represent mean values of 4 independent experiments (with each condition performed in duplicate). Error bars represent SEM. One-way ANOVA followed by Tukey's multiple comparison post hoc test was used to calculate statistical significance. ** P < 0.01; **** P < 0.0001.