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Cited 117 time in webofscience Cited 127 time in scopus
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dc.contributor.authorCho, KS-
dc.contributor.authorPark, HK-
dc.contributor.authorPark, HY-
dc.contributor.authorJung, JS-
dc.contributor.authorJeon, SG-
dc.contributor.authorKim, YK-
dc.contributor.authorRoh, HJ-
dc.date.accessioned2016-04-01T08:33:32Z-
dc.date.available2016-04-01T08:33:32Z-
dc.date.created2009-08-25-
dc.date.issued2009-01-
dc.identifier.issn1066-5099-
dc.identifier.other2009-OAK-0000018458-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/28246-
dc.description.abstractAdipose tissue-derived stem cells (ASCs) exhibit immunosuppressive effects in allogeneic transplantation. However, there is no report that evaluates the in vivo immune-modulating effect of ASCs in an experimental allergic rhinitis (AR) model. We investigated whether ASCs migrate to the nasal mucosa in an AR mouse model and evaluated the immune-modulating effect of ASCs in the AR mouse model. Cultured ASCs (2 x 10(6)) were injected i.v. before the first allergen challenge in the AR mouse model. Migration of ASCs to the nasal mucosa was evaluated by immunofluorescence. The immunomodulatory effects of ASCs were evaluated by nasal symptoms, histology, serum ovalbumin (OVA)-specific antibody, and the cytokine profile of the spleen. ASCs migrated to the nasal mucosa in the AR mouse model. ASCs significantly reduced allergic symptoms and inhibited eosinophilic inflammation in the nasal mucosa. ASCs significantly decreased the serum allergen-specific IgE level and the IgG(1)/IgG(2a) ratio and significantly increased the IgG(2a) level in the AR mouse model. ASCs inhibited interleukin (IL)-4 and IL-5 production from OVA-incubated splenocytes, but enhanced interferon-gamma production. In conclusion, ASCs can migrate to the nasal mucosa in the AR mouse model and inhibit eosinophilic inflammation partly via shifting to a T-helper 1 (Th1) from a Th2 immune response to allergens. STEM CELLS 2009; 27: 259-265-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherALPHAMED PRESS-
dc.relation.isPartOfSTEM CELLS-
dc.subjectImmunosuppression-
dc.subjectAdipose tissue-
dc.subjectStem cells-
dc.subjectMice-
dc.subjectAllergic rhinitis-
dc.subjectHUMAN BONE-MARROW-
dc.subjectSUPPRESS T-LYMPHOCYTE-
dc.subjectDIFFERENTIATION-
dc.subjectPROLIFERATION-
dc.subjectPROSTAGLANDIN-E2-
dc.subjectSECRETION-
dc.subjectRESPONSES-
dc.titleIFATS COLLECTION: IMMUNOMODULATORY EFFECTS OF ADIPOSE TISSUE-DERIVED STEM CELLS IN AN ALLERGIC RHINITIS MOUSE MODEL-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1634/STEMCELLS.20-
dc.author.googleCho, KS-
dc.author.googlePark, HK-
dc.author.googlePark, HY-
dc.author.googleJung, JS-
dc.author.googleJeon, SG-
dc.author.googleKim, YK-
dc.author.googleRoh, HJ-
dc.relation.volume27-
dc.relation.issue1-
dc.relation.startpage259-
dc.relation.lastpage265-
dc.contributor.id10103891-
dc.relation.journalSTEM CELLS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationSTEM CELLS, v.27, no.1, pp.259 - 265-
dc.identifier.wosid000263032400029-
dc.date.tcdate2019-02-01-
dc.citation.endPage265-
dc.citation.number1-
dc.citation.startPage259-
dc.citation.titleSTEM CELLS-
dc.citation.volume27-
dc.contributor.affiliatedAuthorKim, YK-
dc.identifier.scopusid2-s2.0-59849120888-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc76-
dc.type.docTypeArticle-
dc.subject.keywordPlusHUMAN BONE-MARROW-
dc.subject.keywordPlusSUPPRESS T-LYMPHOCYTE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusPROSTAGLANDIN-E2-
dc.subject.keywordPlusSECRETION-
dc.subject.keywordPlusRESPONSES-
dc.subject.keywordAuthorImmunosuppression-
dc.subject.keywordAuthorAdipose tissue-
dc.subject.keywordAuthorStem cells-
dc.subject.keywordAuthorMice-
dc.subject.keywordAuthorAllergic rhinitis-
dc.relation.journalWebOfScienceCategoryCell & Tissue Engineering-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryHematology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaHematology-

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김윤근KIM, YOON KEUN
Dept of Life Sciences
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