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Characterization of ciliated bronchial epithelium 1, a ciliated cell-associated gene induced during mucociliary differentiation.
Yoshisue, Hajime; Puddicombe, Sarah M; Wilson, Susan J; Haitchi, Hans Michael; Powell, Robert M; Wilson, David I; Pandit, Anita; Berger, Ann E; Davies, Donna E; Holgate, Stephen T; Holloway, John W.
Afiliación
  • Yoshisue H; Infection, Inflammation, and Repair Division, University of Southampton School of Medicine, Southampton General Hospital, Southampton, United Kingdom. hyoshisu@soton.ac.uk
Am J Respir Cell Mol Biol ; 31(5): 491-500, 2004 Nov.
Article en En | MEDLINE | ID: mdl-15242845
ABSTRACT
Lung epithelial structure is altered in asthma; however, the precise mechanisms underlying epithelial repair, including differentiation from basal to columnar epithelial cells, are not well defined. In the course of random sequencing of a cDNA library from human lung biopsies, we have identified a novel gene, ciliated bronchial epithelium 1 (CBE1). Expression of CBE1 was induced during in vitro differentiation of bronchial epithelial cells. Synchronous expression with tektin and hepatocyte nuclear factor 3/forkhead homologue 4, down-regulation by interleukin-13, and its tissue distribution strongly suggested that CBE1 is associated with ciliated cells. Two isoforms of the 0.7-kb full-length cDNA were identified, resulting in open reading frames with different carboxyl termini, with no homology to known proteins. Expression of CBE1 in ciliated epithelial cells was confirmed by immunohistochemistry. Quantitative reverse transcription-polymerase chain reaction analysis using bronchial biopsies showed no difference of expression of CBE1 between normal subjects and subjects with asthma. Expression studies showed that CBE1 is nuclear- or perinuclear-localized, depending on cell type. Regulated expression during differentiation and the subcellular localization of CBE1 suggest that it may play an important role in the differentiation and/or function of ciliated cells in human airways.
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Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Bronquios / Proteínas Nucleares / Proteínas de Unión al ADN / Células Epiteliales Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Respir Cell Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2004 Tipo del documento: Article País de afiliación: Reino Unido
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Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Bronquios / Proteínas Nucleares / Proteínas de Unión al ADN / Células Epiteliales Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Respir Cell Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2004 Tipo del documento: Article País de afiliación: Reino Unido