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조승우

Cho, Seung Woo
Genome Engineering Lab.
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dc.citation.endPage 353 -
dc.citation.startPage 341 -
dc.citation.title TISSUE ENGINEERING AND REGENERATIVE MEDICINE -
dc.citation.volume 20 -
dc.contributor.author Park, Jung In -
dc.contributor.author Cho, Seung Woo -
dc.contributor.author Kang, Joo H. -
dc.contributor.author Park, Tae-Eun -
dc.date.accessioned 2023-12-21T12:37:36Z -
dc.date.available 2023-12-21T12:37:36Z -
dc.date.created 2023-05-24 -
dc.date.issued 2023-06 -
dc.description.abstract Backgound:Considering the important role of the Peyer's patches (PPs) in gut immune balance, understanding of the detailed mechanisms that control and regulate the antigens in PPs can facilitate the development of immune therapeutic strategies against the gut inflammatory diseases.Methods:In this review, we summarize the unique structure and function of intestinal PPs and current technologies to establish in vitro intestinal PP system focusing on M cell within the follicle-associated epithelium and IgA(+) B cell models for studying mucosal immune networks. Furthermore, multidisciplinary approaches to establish more physiologically relevant PP model were proposed.Results:PPs are surrounded by follicle-associated epithelium containing microfold (M) cells, which serve as special gateways for luminal antigen transport across the gut epithelium. The transported antigens are processed by immune cells within PPs and then, antigen-specific mucosal immune response or mucosal tolerance is initiated, depending on the response of underlying mucosal immune cells. So far, there is no high fidelity (patho)physiological model of PPs; however, there have been several efforts to recapitulate the key steps of mucosal immunity in PPs such as antigen transport through M cells and mucosal IgA responses.Conclusion:Current in vitro PP models are not sufficient to recapitulate how mucosal immune system works in PPs. Advanced three-dimensional cell culture technologies would enable to recapitulate the function of PPs, and bridge the gap between animal models and human. -
dc.identifier.bibliographicCitation TISSUE ENGINEERING AND REGENERATIVE MEDICINE, v.20, pp.341 - 353 -
dc.identifier.doi 10.1007/s13770-023-00543-y -
dc.identifier.issn 1738-2696 -
dc.identifier.scopusid 2-s2.0-85153363949 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/64343 -
dc.identifier.wosid 000975573900003 -
dc.language 영어 -
dc.publisher KOREAN TISSUE ENGINEERING REGENERATIVE MEDICINE SOC -
dc.title Intestinal Peyer's Patches: Structure, Function, and In Vitro Modeling -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Cell & Tissue Engineering; Engineering, Biomedical -
dc.relation.journalResearchArea Cell Biology; Engineering -
dc.type.docType Review; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.subject.keywordAuthor Peyer&apos -
dc.subject.keywordAuthor s patches -
dc.subject.keywordAuthor M-cell -
dc.subject.keywordAuthor Mucosal immunity -
dc.subject.keywordAuthor In vitro Peyer&apos -
dc.subject.keywordAuthor s patch model -
dc.subject.keywordPlus M-CELL MODEL -
dc.subject.keywordPlus INFLAMMATORY-BOWEL-DISEASE -
dc.subject.keywordPlus HUMAN B-CELLS -
dc.subject.keywordPlus DENDRITIC CELLS -
dc.subject.keywordPlus IGA PRODUCTION -
dc.subject.keywordPlus ESCHERICHIA-COLI -
dc.subject.keywordPlus FIMH(+) BACTERIA -
dc.subject.keywordPlus GLYCOPROTEIN 2 -
dc.subject.keywordPlus CHOLERA-TOXIN -
dc.subject.keywordPlus TGF-BETA -

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