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. 2020 Jan 23;11(1):53. doi: 10.1038/s41419-020-2237-2

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© The Author(s) 2020

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — Cultured RAW264.7 (a, b) and BMDM (c, d) were stimulated as described in the Materials and methods section, and mRNA of the markers CD38 and NOS2 was analyzed by QRT-PCR. Fold increase over unstimulated cells, C = control, no stimulation; n = 3; *p < 0.05. Cultured RAW264.7 (e, f) and BMDM (g, h) were stimulated as described in the Materials and methods section, and mRNA of the markers Egr-2 and Arg1 was analyzed by QRT-PCR. Fold increase over unstimulated cells, C = control, no stimulation; n = 3; *p < 0.05.