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. 2024 May 22;630(8016):360–367. doi: 10.1038/s41586-024-07426-9

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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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Extended Data Fig. 10 — a, Schematic illustration for the study design based on the porcine model. b, Representative histology images stained with Masson’s trichrome (MTS) and haematoxylin and eosin (H&E) for native tissue (left), adhesive implant (middle), and non-adhesive implant (right) collected on 7 days post-implantation to the small intestine. Black dotted lines in images indicate the implant-tissue interface; yellow dotted lines in images indicate the fibrous capsule-tissue interface. The experiment was repeated independently (n = 4 per group) with similar results. The graphic of the pig in a was created with BioRender.com.