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Cited 33 time in webofscience Cited 65 time in scopus
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Microchannel network hydrogel induced ischemic blood perfusion connection

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dc.contributor.authorJung Bok Lee-
dc.contributor.authorDae-Hyun Kim-
dc.contributor.authorJeong-Kee Yoon-
dc.contributor.authorDan Bi Park-
dc.contributor.authorHye-Seon Kim-
dc.contributor.authorYoung Min Shin-
dc.contributor.authorWooyeol Baek-
dc.contributor.authorMi-Lan Kang-
dc.contributor.authorHyun Jung Kim-
dc.contributor.authorHak-Joon Sung-
dc.date.accessioned2023-04-21T01:40:18Z-
dc.date.available2023-04-21T01:40:18Z-
dc.date.issued2020-01-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://yscholarhub.yonsei.ac.kr/handle/2021.sw.yonsei/6612-
dc.description.abstractAngiogenesis induction into damaged sites has long been an unresolved issue. Local treatment with pro-angiogenic molecules has been the most common approach. However, this approach has critical side effects including inflammatory coupling, tumorous vascular activation, and off-target circulation. Here, the concept that a structure can guide desirable biological function is applied to physically engineer three-dimensional channel networks in implant sites, without any therapeutic treatment. Microchannel networks are generated in a gelatin hydrogel to overcome the diffusion limit of nutrients and oxygen three-dimensionally. Hydrogel implantation in mouse and porcine models of hindlimb ischemia rescues severely damaged tissues by the ingrowth of neighboring host vessels with microchannel perfusion. This effect is guided by microchannel size-specific regenerative macrophage polarization with the consequent functional recovery of endothelial cells. Multiple-site implantation reveals hypoxia and neighboring vessels as major causative factors of the beneficial function. This technique may contribute to the development of therapeutics for hypoxia/inflammatory-related diseases. © 2020, The Author(s).-
dc.language영어-
dc.language.isoENG-
dc.publisherNature Research-
dc.titleMicrochannel network hydrogel induced ischemic blood perfusion connection-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1038/s41467-020-14480-0-
dc.identifier.scopusid2-s2.0-85078713603-
dc.identifier.wosid000543985100001-
dc.identifier.bibliographicCitationNature Communications, v.11, no.1-
dc.citation.titleNature Communications-
dc.citation.volume11-
dc.citation.number1-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusblood-
dc.subject.keywordPluscell component-
dc.subject.keywordPlusdisease-
dc.subject.keywordPlushypoxia-
dc.subject.keywordPlusinduced response-
dc.subject.keywordPlusprotein-
dc.subject.keywordPlusSus-
dc.subject.keywordAuthorhydrogel-
dc.subject.keywordAuthorAngiogenesis-
dc.subject.keywordAuthorthree-dimensional channel networks-
dc.subject.keywordAuthorhypoxia/inflammatory-related diseases-
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