Mucin gene expression in rhinitis syndromes

被引:1
|
作者
Asunción Martínez-Antón
Jordi Roca-Ferrer
Joaquim Mullol
机构
[1] Hospital Clínic,Unitat de Rinologia, Servei d’Otorinolaringologia
来源
Current Allergy and Asthma Reports | 2006年 / 6卷
关键词
Cystic Fibrosis; Allergic Rhinitis; Allergic Rhinitis; Goblet Cell; Cystic Fibrosis Patient;
D O I
暂无
中图分类号
学科分类号
摘要
Rhinitis and rhinosinusitis are often associated with airway diseases such as asthma, cystic fibrosis, and nasal polyposis. In these diseases, the alteration of both the quantity and quality of mucus results in an impaired mucociliary clearance, and this produces, in extreme cases, the airway obstruction. Mucins are the major component in mucus and are responsible for its viscoelastic properties. Mucin expression patterns have been shown to be altered in rhinitis-associated diseases. It has been proposed that this is one of the causes of hyperviscid mucus plugs in these pathologies. For this reason, the study of mucin expression and regulation in upper- and lower-airway diseases, such as asthma, cystic fibrosis, and nasal polyposis, may be crucial for the development of new therapies against mucus hypersecretion. In this review, we report major findings regarding mucin expression and regulation in rhinitis syndromes.
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收藏
页码:189 / 197
页数:8
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