Analysis of eosinophil granule proteins in ECRS
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- Tsuda Takeshi
- Department of Otorhinolaryngology–Head and Neck Surgery, Osaka University Graduate School of Medicine
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- Maeda Yohei
- Department of Otorhinolaryngology–Head and Neck Surgery, Osaka University Graduate School of Medicine
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- Hayama Masaki
- Department of Otorhinolaryngology–Head and Neck Surgery, Osaka University Graduate School of Medicine
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- Takeda Kazuya
- Department of Otolaryngology, Osaka City General Hospital
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- Inohara Hidenori
- Department of Otorhinolaryngology–Head and Neck Surgery, Osaka University Graduate School of Medicine
Bibliographic Information
- Other Title
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- 好酸球性副鼻腔炎における好酸球顆粒蛋白の機能解析
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Description
<p>Eosinophilic chronic rhinosinusitis (ECRS) is a subtype of chronic rhinosinusitis (CRS) that is characterized by eosinophilic nasal polyposis. Because several types of cells play a role in pathogenesis, ECRS is a heterogenous disease. To identify each cell function is important for the individualization of therapy. The eosinophil is a granulocyte that contain eosinophil granule proteins (EGPs). EGPs have antiparasitic activity, on the other hand, closely related allergic inflammation due to its cytotoxicity. Eosinophil-derived neurotoxin (EDN) is one of the eosinophil granule proteins. In this study, we evaluated the function of EDN in ECRS pathogenesis. Serum EDN levels were significantly higher in patients with ECRS than in those with other nasal and paranasal diseases and were positively correlated with clinical disease activity. EDN expressed in the eosinophils of ECRS nasal polyps. Human nasal epithelial cells (HNEpCs) were stimulated with EDN, and the resultant changes in gene expression were detected by RNA sequencing. Pathway analysis revealed that the major canonical pathway affected by EDN stimulation was “regulation of the epithelial–mesenchymal transition (EMT) pathway”; the only gene in this pathway to be up-regulated was matrix metalloproteinase 9 (MMP-9). EDN may be involved in the pathogenesis of ECRS and also be an important therapeutic target.</p>
Journal
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- Journal of Japan Society of Immunology & Allergology in Otolaryngology
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Journal of Japan Society of Immunology & Allergology in Otolaryngology 37 (3), 223-228, 2019
JAPAN SOCIETY OF IMMUNOLOGY AND ALLERGOLOGY IN OTOLARYNGOLOGY
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Details 詳細情報について
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- CRID
- 1390845702281113600
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- NII Article ID
- 130007709685
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- ISSN
- 21855900
- 09130691
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed