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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. 4 — a, Schematic illustrations of the adhesive implant with sutures at the corners. b, Representative histology image stained with haematoxylin and eosin (H&E) for the adhesive implant with sutures on the abdominal wall collected on day 28 post-implantation. c,d, Representative histology images stained with Masson’s trichrome (MTS, left) and H&E (right) for the suture point (c) and the intact adhesive-tissue interface (d) collected on day 28 post-implantation to the abdominal wall. *In images indicates the implant; black dotted lines indicate the implant-tissue interface. FC, fibrous capsule. The experiment in b–d was repeated independently (n = 6) with similar results.