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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. 2 — a, Representative histology images stained with Masson’s trichrome (MTS, left) and haematoxylin and eosin (H&E, right) of the adhesive implant collected on day 28 post-implantation to the abdominal wall. Black and red dotted areas indicate the implant-tissue interface and the implant-abdominal cavity interface, respectively. b,c, Representative histology images stained with MTS (left) and H&E (right) of the implant-tissue interface (b) and implant-cavity interface (c) for the adhesive implant collected on day 28 post-implantation to the abdominal wall. The experiment was repeated independently (n = 4) with similar results.