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. 2023 Jul 25;9:77. doi: 10.1038/s41421-023-00578-4

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© The Author(s) 2023

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. 6 — a, b Representative IF images of Apoa1, Saa1, Muc2 and Ido1 in the mouse ileum. Scale bars, 20 μm. c q-PCR analysis of mRNA levels in mouse intestinal (means ± SD, two-way ANOVA. *P < 0.05. **P < 0.01. ***P < 0.001. ****P < 0.0001, n = 5–7 mice, same as below). d Representative immunohistochemistry (IHC) images of ZO-1 in the mouse intestine. Scale bars, 100 μm. e q-PCR analysis of ZO-1 and Occludin mRNA levels in mouse intestinal. f P38, p-P38, JNK and p-JNK expression in mouse liver and intestinal, as analyzed by western blotting assay. g q-PCR analysis of mRNA levels in mouse liver.