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- Publisher Website: 10.1053/rmed.2002.1413
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- PMID: 12556012
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Article: Down-regulation of aquaporin 3 in bronchiectatic airways in vivo
Title | Down-regulation of aquaporin 3 in bronchiectatic airways in vivo |
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Authors | |
Keywords | Aquaporins Bronchial biopsy Bronchiectasis Immunohistochemistry Mucus |
Issue Date | 2003 |
Publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rmed |
Citation | Respiratory Medicine, 2003, v. 97 n. 1, p. 59-64 How to Cite? |
Abstract | Bronchiectasis is characterized pathologically by permanent abnormal bronchial dilation, and clinically by chronic sputum production. Aquaporin 3 (AQP3), a recently described water channel that is also found in large airway cell membrane, could play a role in the pathogenesis and particularly that of bronchorrhea in bronchiectasis. However, little is known of its in vivo distribution and physiological role in human airways. We have, therefore, performed this quantitative immunohistochemistry study on endobronchial biopsies to evaluate the expression and clinical relevance of AQP3 in patients with idiopathic bronchiectasis (n = 25, 15 F, 64.3 ± 11.5 years) and control subjects (n = 14, 5 F, 57.5 ± 12.0 years). Quantitative image analysis was performed to evaluate the expression of AQP3 in the bronchial epithelial cells. Our results show that AQP3 was predominantly expressed in the basal cells of the epithelial layer in both groups. Expression of AQP3 was significantly reduced in the basal, but not columnar, epithelial cells in bronchiectasis compared with control airways (p = 0.02, 0.35). Only bronchiectatic patients with regular sputum production, but not their counterparts, had significant downregulation of epithelial AQP3 expression compared with control airways (p = 0.004, 0.24). Our findings suggest that AQP3 could have an important role in the pathogenesis of increased mucus production in bronchiectasis. © 2002 Elsevier Science Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/67953 |
ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 1.180 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tsang, KW | en_HK |
dc.contributor.author | Leung, JC | en_HK |
dc.contributor.author | Tipoe, GL | en_HK |
dc.contributor.author | Leung, R | en_HK |
dc.contributor.author | Yan, C | en_HK |
dc.contributor.author | Ooi, GC | en_HK |
dc.contributor.author | Chan, HH | en_HK |
dc.contributor.author | Lam, WK | en_HK |
dc.contributor.author | Lai, KN | en_HK |
dc.date.accessioned | 2010-09-06T05:59:46Z | - |
dc.date.available | 2010-09-06T05:59:46Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | Respiratory Medicine, 2003, v. 97 n. 1, p. 59-64 | en_HK |
dc.identifier.issn | 0954-6111 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/67953 | - |
dc.description.abstract | Bronchiectasis is characterized pathologically by permanent abnormal bronchial dilation, and clinically by chronic sputum production. Aquaporin 3 (AQP3), a recently described water channel that is also found in large airway cell membrane, could play a role in the pathogenesis and particularly that of bronchorrhea in bronchiectasis. However, little is known of its in vivo distribution and physiological role in human airways. We have, therefore, performed this quantitative immunohistochemistry study on endobronchial biopsies to evaluate the expression and clinical relevance of AQP3 in patients with idiopathic bronchiectasis (n = 25, 15 F, 64.3 ± 11.5 years) and control subjects (n = 14, 5 F, 57.5 ± 12.0 years). Quantitative image analysis was performed to evaluate the expression of AQP3 in the bronchial epithelial cells. Our results show that AQP3 was predominantly expressed in the basal cells of the epithelial layer in both groups. Expression of AQP3 was significantly reduced in the basal, but not columnar, epithelial cells in bronchiectasis compared with control airways (p = 0.02, 0.35). Only bronchiectatic patients with regular sputum production, but not their counterparts, had significant downregulation of epithelial AQP3 expression compared with control airways (p = 0.004, 0.24). Our findings suggest that AQP3 could have an important role in the pathogenesis of increased mucus production in bronchiectasis. © 2002 Elsevier Science Ltd. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rmed | en_HK |
dc.relation.ispartof | Respiratory Medicine | en_HK |
dc.subject | Aquaporins | en_HK |
dc.subject | Bronchial biopsy | en_HK |
dc.subject | Bronchiectasis | en_HK |
dc.subject | Immunohistochemistry | en_HK |
dc.subject | Mucus | en_HK |
dc.subject.mesh | Aquaporin 3 | en_HK |
dc.subject.mesh | Aquaporins - metabolism | en_HK |
dc.subject.mesh | Bronchi - metabolism | en_HK |
dc.subject.mesh | Bronchiectasis - metabolism - physiopathology | en_HK |
dc.subject.mesh | Down-Regulation | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Forced Expiratory Volume - physiology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunohistochemistry | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Vital Capacity - physiology | en_HK |
dc.title | Down-regulation of aquaporin 3 in bronchiectatic airways in vivo | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0954-6111&volume=97&issue=1&spage=59&epage=64&date=2003&atitle=Down-regulation+of+aquaporin+3+in+bronchiectatic+airways+in+vivo | en_HK |
dc.identifier.email | Leung, JC: jckleung@hku.hk | en_HK |
dc.identifier.email | Tipoe, GL: tgeorge@hkucc.hku.hk | en_HK |
dc.identifier.email | Lai, KN: knlai@hku.hk | en_HK |
dc.identifier.authority | Leung, JC=rp00448 | en_HK |
dc.identifier.authority | Tipoe, GL=rp00371 | en_HK |
dc.identifier.authority | Lai, KN=rp00324 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1053/rmed.2002.1413 | en_HK |
dc.identifier.pmid | 12556012 | - |
dc.identifier.scopus | eid_2-s2.0-0037232627 | en_HK |
dc.identifier.hkuros | 79047 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0037232627&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 97 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 59 | en_HK |
dc.identifier.epage | 64 | en_HK |
dc.identifier.isi | WOS:000180514900009 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Tsang, KW=7201555024 | en_HK |
dc.identifier.scopusauthorid | Leung, JC=7202180349 | en_HK |
dc.identifier.scopusauthorid | Tipoe, GL=7003550610 | en_HK |
dc.identifier.scopusauthorid | Leung, R=7101876102 | en_HK |
dc.identifier.scopusauthorid | Yan, C=8728540500 | en_HK |
dc.identifier.scopusauthorid | Ooi, GC=7006176119 | en_HK |
dc.identifier.scopusauthorid | Chan, HH=24555248900 | en_HK |
dc.identifier.scopusauthorid | Lam, WK=7203021937 | en_HK |
dc.identifier.scopusauthorid | Lai, KN=7402135706 | en_HK |
dc.identifier.issnl | 0954-6111 | - |