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However, it requires scalable and robust, but fully defined culture platforms free of xenogeneic components. Most existing systems, however, typically rely on Matrigel, which complicates clinical translation and limits understanding of stem cell\u2010material interactions. Here, a poly(ethyleneglycoldimethacrylate) (pEGDMA)\u2010based synthetic culture surface is exposed to N\n                    <jats:sub>2<\/jats:sub>\n                    plasma treatment for tailored modulation of surface properties. This modification enhances surface wettability and introduces N\u2010containing functional groups, resulting in a PoLymer\u2010coated Ultra\u2010stable Surface (PLUS) that improves ISC attachment under xenogeneic\u2010free culture conditions. Remarkably, PLUS maintains its ISC\u2010supportive function even after 3 years of ambient storage. Gene expression and proteomic analyses reveal upregulation of factors involved in actin dynamics and cytoskeletal reorganization. Consistently, colonies on PLUS exhibit a broader migratory range, with a 1.8\u2010fold increase in migration speed compared to pristine pEGDMA. Small\u2010molecule perturbation assays confirm the involvement of cytoskeletal remodelling by mediating ISC\u2010substrate interaction. Furthermore, PLUS supports dynamic, actin\u2010dependent migration, enabling up to 46.7% wound closure within 144\u00a0h. These findings demonstrate that PLUS engages cytoskeletal machinery as a central mediator of ISC\u2010substrate interaction, in part by promoting actin\u2010dependent cytoskeletal reorganization, positioning it as a scalable, translational platform for ISC\u2010based regenerative medicine.\n                  <\/jats:p>","DOI":"10.1002\/adma.202513371","type":"journal-article","created":{"date-parts":[[2025,11,26]],"date-time":"2025-11-26T08:40:15Z","timestamp":1764146415000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Tailored Xenogeneic\u2010Free Polymer Surface Promotes Dynamic Migration of Intestinal Stem Cells"],"prefix":"10.1002","volume":"38","author":[{"given":"Seonghyeon","family":"Park","sequence":"first","affiliation":[{"name":"Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and Technology (KAIST)  291 Daehak\u2010ro, Yuseong\u2010gu Daejeon 34141 Republic of 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Daejeon 34141 Republic of Korea"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Minkyung","family":"Kim","sequence":"additional","affiliation":[{"name":"Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and Technology (KAIST)  291 Daehak\u2010ro, Yuseong\u2010gu Daejeon 34141 Republic of Korea"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7590-8812","authenticated-orcid":false,"given":"Mi\u2010Young","family":"Son","sequence":"additional","affiliation":[{"name":"Bionanotechnology Research Center Korea Research Institute of Bioscience and Biotechnology (KRIBB)  125 Gwahak\u2010ro, Yuseong\u2010gu Daejeon 34141 Republic of Korea"},{"name":"KRIBB School of Bioscience Korea University of Science and Technology (UST)  Daejeon 34141 Republic of Korea"},{"name":"School of Medicine Sungkyunkwan University 2066 Seobu\u2010ro Suwon 16419 Republic of 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