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. 2024 Nov 28;14:29627. doi: 10.1038/s41598-024-81304-2

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© The Author(s) 2024

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 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/.

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Fig. 5 — S-Allylmercaptocysteine (SAMC) induces the gene expression of MyD88-S. (a) Real-time qPCR analysis of the effect of SAMC (300 µM) on mRNA expression of Myd88s in HC11 cells upon lipopolysaccharide (LPS) stimulation (100 ng/mL) for 30–120 min. (b, c) Real-time qPCR analysis of the concentration-dependent effect of SAMC (10–300 µM) on mRNA expression of Myd88s (b) and canonical Myd88l (c) in HC11 cells treated with LPS for 2 h. Data are shown as mean ± SD, n = 4–5. ** denotes significant difference (p < 0.01) and * denotes significant difference (p < 0.05).