NLRP3 inflammasome activation by mitochondrial ROS in bronchial epithelial cells is required for allergic inflammation.
DC Field | Value | Language |
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dc.contributor.author | Kim, S. R. | - |
dc.contributor.author | Kim, D. I. | - |
dc.contributor.author | Kim, S. H. | - |
dc.contributor.author | Lee, Hyun | - |
dc.contributor.author | Lee, K. S. | - |
dc.contributor.author | Cho, S. H. | - |
dc.contributor.author | Lee, Y. C. | - |
dc.date.accessioned | 2022-07-16T02:32:26Z | - |
dc.date.available | 2022-07-16T02:32:26Z | - |
dc.date.created | 2021-05-13 | - |
dc.date.issued | 2014-10 | - |
dc.identifier.issn | 2041-4889 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/158877 | - |
dc.description.abstract | Abnormality in mitochondria has been suggested to be associated with development of allergic airway disorders. In this study, to evaluate the relationship between mitochondrial reactive oxygen species (ROS) and NLRP3 inflammasome activation in allergic asthma, we used a newly developed mitochondrial ROS inhibitor, NecroX-5. NecroX-5 reduced the increase of mitochondrial ROS generation in airway inflammatory cells, as well as bronchial epithelial cells, NLRP3 inflammasome activation, the nuclear translocation of nuclear factor-kappa B, increased expression of various inflammatory mediators and pathophysiological features of allergic asthma in mice. Finally, blockade of IL-1 beta substantially reduced airway inflammation and hyperresponsiveness in the asthmatic mice. These findings suggest that mitochondrial ROS have a critical role in the pathogenesis of allergic airway inflammation through the modulation of NLRP3 inflammasome activation, providing a novel role of airway epithelial cells expressing NLRP3 inflammasome as an immune responder. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | NATURE PUBLISHING GROUP | - |
dc.title | NLRP3 inflammasome activation by mitochondrial ROS in bronchial epithelial cells is required for allergic inflammation. | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, Hyun | - |
dc.identifier.doi | 10.1038/cddis.2014.460 | - |
dc.identifier.scopusid | 2-s2.0-84921966782 | - |
dc.identifier.wosid | 000344994000069 | - |
dc.identifier.bibliographicCitation | CELL DEATH & DISEASE, v.5, no.10, pp.1 - 15 | - |
dc.relation.isPartOf | CELL DEATH & DISEASE | - |
dc.citation.title | CELL DEATH & DISEASE | - |
dc.citation.volume | 5 | - |
dc.citation.number | 10 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 15 | - |
dc.type.rims | ART | - |
dc.type.docType | 정기학술지(Article(Perspective Article포함)) | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Cell Biology | - |
dc.relation.journalWebOfScienceCategory | Cell Biology | - |
dc.subject.keywordPlus | NALP3 INFLAMMASOME | - |
dc.subject.keywordPlus | REACTIVE OXYGEN | - |
dc.subject.keywordPlus | AIRWAY HYPERRESPONSIVENESS | - |
dc.subject.keywordPlus | OXIDATIVE STRESS | - |
dc.subject.keywordPlus | LUNG-DISEASES | - |
dc.subject.keywordPlus | KAPPA-B | - |
dc.subject.keywordPlus | ASTHMA | - |
dc.subject.keywordPlus | CYTOKINES | - |
dc.subject.keywordPlus | MICE | - |
dc.subject.keywordPlus | GENERATION | - |
dc.identifier.url | https://www.nature.com/articles/cddis2014460 | - |
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