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  1. Dokkyo Journal of Medical Sciences
  2. 31(1) 2004

Airway Expression of Smad7, a TGF-β-inducible Inhibitory Molecule of TGF-β Signaling, Decreases after Repeated Airway Antigen Challenges

https://dmu.repo.nii.ac.jp/records/214
https://dmu.repo.nii.ac.jp/records/214
631d9d07-5752-428b-a4b5-31974a6e0f85
名前 / ファイル ライセンス アクション
KJ00004091307.pdf KJ00004091307.pdf (851.3 kB)
Item type [ELS]学術雑誌論文 / Journal Article(1)
公開日 2017-05-24
タイトル
言語 en
タイトル Airway Expression of Smad7, a TGF-β-inducible Inhibitory Molecule of TGF-β Signaling, Decreases after Repeated Airway Antigen Challenges
言語
言語 eng
キーワード
言語 en
主題 Smad 7
キーワード
言語 en
主題 chronic asthma
キーワード
言語 en
主題 bronchial epithelial cells
キーワード
言語 en
主題 airway remodeling
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
雑誌書誌ID
収録物識別子 AA00629581
論文名よみ
タイトル Airway Expression of Smad7, a TGF-β-inducible Inhibitory Molecule of TGF-β Signaling, Decreases after Repeated Airway Antigen Challenges
著者 Ota, Mayumi

× Ota, Mayumi

WEKO 741

en Ota, Mayumi

Search repository
Nakao, Atsuhito

× Nakao, Atsuhito

WEKO 742

en Nakao, Atsuhito

Search repository
Sugiyama, Kumiya

× Sugiyama, Kumiya

WEKO 743

en Sugiyama, Kumiya

Search repository
Cheng, Gang

× Cheng, Gang

WEKO 744

en Cheng, Gang

Search repository
Akimoto, Kazumi

× Akimoto, Kazumi

WEKO 745

en Akimoto, Kazumi

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Okada, Takenori

× Okada, Takenori

WEKO 746

en Okada, Takenori

Search repository
Sagara, Hironori

× Sagara, Hironori

WEKO 747

en Sagara, Hironori

Search repository
著者所属(英)
en
Department of Pulmonary Medicine and Clinical Immunology, Dokkyo University School of Medicine
著者所属(英)
en
Department of Parasitology and Immunology, University ofYamanashi Faculty of Medicine
著者所属(英)
en
Department of Pulmonary Medicine and Clinical Immunology, Dokkyo University School of Medicine
著者所属(英)
en
Department of Pulmonary Medicine and Clinical Immunology, Dokkyo University School of Medicine
著者所属(英)
en
Laboratory of Molecular and Cellular Biology, Dokkyo University School of Medicine
著者所属(英)
en
Department of Pulmonary Medicine and Clinical Immunology, Dokkyo University School of Medicine
著者所属(英)
en
Department of Pulmonary Medicine and Clinical Immunology, Dokkyo University School of Medicine
記事種別(日)
内容記述タイプ Other
内容記述 原著
記事種別(英)
内容記述タイプ Other
内容記述 Original
抄録(英)
内容記述タイプ Other
内容記述 Transforming growth factor-β (TGF-β) is a profibrogenic cytokine that is involved in airway remodeling largely associated with chronic asthma. Accordingly, regulators of TGF-β activity could also play some role in airway remodeling in asthma. In this study, we investigated expression of Smad 7, a major intracellular inhibitor of TGF-β signaling, in the airways of mouse models of acute and chronic asthma. Sensitized, repeatedly (14 days) ovalbumin (OVA)-inhaled BALB/c mice exhibited evidence of airway remodeling including prominent subepithelial fibrosis associated with airway hyperresponsiveness (AHR) and airway inflammation (chronic asthma model) whereas sensitized, shortly OVA-inhaled BALB/c mice showed only AHR and airway inflammation (acute asthma model). Immunohistochemical analysis showed that Smad 7 immunoreactivity in the airways was increased after the development of acute and chronic asthma models and mainly detected in bronchial epithelial cells. Interestingly, Smad 7 immunoreactivity was significantly less in the airways of chronic asthma model than in those of acute asthma model, which was also confirmed by real-time PCR analysis of Smad 7. In consistent with decreased Smad 7 expression in the airways of chronic asthma model, phosphorylation of Smad 2, a marker of active TGF-β signaling, was increased in bronchial epithelial cells of chronic asthma model when compared with acute asthma model. These results suggest that decreased Smad 7 expression and Smad 2 upregulation in bronchial epithelial cells might result in increased TGF-β activity and contribute to the development of airway remodeling seen in chronic asthma.
書誌情報 Dokkyo journal of medical sciences

巻 31, 号 1, p. 17-26, 発行日 2004-03-25
ISSN
収録物識別子 03855023
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