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Role of club cell 16-kDa secretory protein in asthmatic airways
DC Field | Value | Language |
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dc.contributor.author | Jung, CG | - |
dc.contributor.author | Cao, TBT | - |
dc.contributor.author | Quoc, QL | - |
dc.contributor.author | Yang, EM | - |
dc.contributor.author | Ban, GY | - |
dc.contributor.author | Park, HS | - |
dc.date.accessioned | 2023-07-06T06:02:51Z | - |
dc.date.available | 2023-07-06T06:02:51Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 0954-7894 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/26133 | - |
dc.description.abstract | Background: Club cell 16-kDa secretory protein (CC16) is a pneumoprotein and functions as an anti-inflammatory or antioxidant protein. However, altered levels of serum CC16 as well as their effect on airways inflammation have not been fully evaluated. Methods: We recruited 63 adult asthmatics on maintenance medications and 61 healthy controls (HCs). The asthmatic subjects were divided into two groups according to the result of bronchodilator responsiveness (BDR) test: the present BDR (n = 17) and absent BDR (n = 46) groups. Serum CC16 levels were measured by ELISA. As an in vitro study, the effect of Dermatophagoides pteronyssinus antigen 1 (Der p1) on the production of CC16 in airways epithelial cells (AECs) according to a time-dependent manner was assessed; the effects of CC16 protein on oxidative stress system, airways inflammation and remodelling were tested. Results: Serum CC16 levels showed significantly higher in the asthmatics than in the HCs (p <.001) with a positive correlation with FEV1% (r =.352, p =.005). The present BDR group had significantly lower levels of serum CC16, FEV1% and MMEF%, but showed higher level of FeNO than the absent BDR group. Serum CC16 levels (below 496.0 ng/mL) could discriminate the present BDR group from the absent BDR group (area under the curve = 0.74, p =.004). In vitro testing demonstrated that Der p1 exposure significantly induced CC16 release from AECs for 1 h, which was progressively decreased after 6 h and followed by MMP-9 and TIMP-1 production. These findings were associated with oxidant/antioxidant disequilibrium and restored by CC16 treatment (but not dexamethasone). Conclusion: Decreased CC16 production contributes to persistent airways inflammation and lung function decline. CC16 may be a potential biomarker for asthmatics with BDR. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Antioxidants | - |
dc.subject.MESH | Asthma | - |
dc.subject.MESH | Bronchodilator Agents | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Inflammation | - |
dc.subject.MESH | Proteins | - |
dc.subject.MESH | Respiratory Function Tests | - |
dc.subject.MESH | Uteroglobin | - |
dc.title | Role of club cell 16-kDa secretory protein in asthmatic airways | - |
dc.type | Article | - |
dc.identifier.pmid | 37009718 | - |
dc.subject.keyword | airways obstruction | - |
dc.subject.keyword | asthma | - |
dc.subject.keyword | CC16 | - |
dc.subject.keyword | house dust mite | - |
dc.subject.keyword | inflammation | - |
dc.subject.keyword | remodelling | - |
dc.subject.keyword | small airways dysfunction | - |
dc.contributor.affiliatedAuthor | Park, HS | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1111/cea.14315 | - |
dc.citation.title | Clinical and experimental allergy | - |
dc.citation.volume | 53 | - |
dc.citation.number | 6 | - |
dc.citation.date | 2023 | - |
dc.citation.startPage | 648 | - |
dc.citation.endPage | 658 | - |
dc.identifier.bibliographicCitation | Clinical and experimental allergy, 53(6). : 648-658, 2023 | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.identifier.eissn | 1365-2222 | - |
dc.relation.journalid | J009547894 | - |
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