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Cited 12 time in webofscience Cited 10 time in scopus
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Roles of Periostin in Symptom Manifestation and Airway Remodeling in a Murine Model of Allergic Rhinitis

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dc.contributor.authorHur, Dong Gu-
dc.contributor.authorKhalmuratova, Roza-
dc.contributor.authorAhn, Seong-Ki-
dc.contributor.authorHa, Young-Sool-
dc.contributor.authorMin, Yang-Gi-
dc.date.accessioned2022-12-27T01:45:28Z-
dc.date.available2022-12-27T01:45:28Z-
dc.date.issued2012-07-
dc.identifier.issn2092-7355-
dc.identifier.issn2092-7363-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/22112-
dc.description.abstractPurpose: Periostin was originally identified as a secreted factor during screening of a mouse osteoblastic library. In a recent study, periostin was found to directly regulate eosinophil accumulation in allergic mucosal inflammation. Chronic eosinophilic inflammation is related to the development of remodeling. The present study examined the expression of periostin and evaluated its role in the inflammatory process and remodeling associated with allergic rhinitis. Methods: A murine model of allergic rhinitis was established in periostin knockout mice. We analyzed the expression of periostin, manifestation of nasal symptoms, eosinophilic inflammation, and subepithelial fibrosis as well as the expression of MMP-2, TIMP-1, and type 1 collagen in nasal tissue. Results: Periostin was mainly distributed in the subepithelial tissue of the nasal mucosa. The subepithelial tissue was thinner in the knockout group than in the control group. No differences in the expression of MMP-2 or TIMP-1 were found in the knockout group. However, after a month of allergen challenge, type I collagen in the nasal tissue was lower in the knockout group than in the control group. The number of eosinophils and the symptom score were also lower in the knockout group. Conclusions: Periostin is expressed in nasal tissues of murine models of allergic rhinitis. Periostin deficiency may affect the remodeling of nasal tissue with reduced subepithelial fibrosis, and lead to less eosinophilic inflammation.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN ACAD ASTHMA ALLERGY & CLINICAL IMMUNOLOGY-
dc.titleRoles of Periostin in Symptom Manifestation and Airway Remodeling in a Murine Model of Allergic Rhinitis-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4168/aair.2012.4.4.222-
dc.identifier.scopusid2-s2.0-84863876706-
dc.identifier.wosid000305777400009-
dc.identifier.bibliographicCitationALLERGY ASTHMA & IMMUNOLOGY RESEARCH, v.4, no.4, pp 222 - 230-
dc.citation.titleALLERGY ASTHMA & IMMUNOLOGY RESEARCH-
dc.citation.volume4-
dc.citation.number4-
dc.citation.startPage222-
dc.citation.endPage230-
dc.type.docTypeArticle-
dc.identifier.kciidART001668510-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskciCandi-
dc.relation.journalResearchAreaAllergy-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryAllergy-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusGROWTH-FACTOR-BETA-
dc.subject.keywordPlusOSTEOBLAST-SPECIFIC FACTOR-
dc.subject.keywordPlusBASEMENT-MEMBRANE ZONE-
dc.subject.keywordPlusSUBEPITHELIAL FIBROSIS-
dc.subject.keywordPlusBRONCHIAL-ASTHMA-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusFASCICLIN-I-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusEOSINOPHILS-
dc.subject.keywordPlusADHESION-
dc.subject.keywordAuthorAirway remodeling-
dc.subject.keywordAuthorallergy-
dc.subject.keywordAuthoreosinophils-
dc.subject.keywordAuthormice-
dc.subject.keywordAuthorperiostin protein-
dc.subject.keywordAuthorrhinitis-
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