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FGF and EDA pathways control initiation and branching of distinct subsets of developing nasal glands.
May, Alison J; Headon, Denis; Rice, David P; Noble, Alistair; Tucker, Abigail S.
Afiliación
  • May AJ; Department of Craniofacial Development and Stem Cell Biology, Guy's Hospital, King's College London, United Kingdom.
  • Headon D; The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.
  • Rice DP; Orthodontics, Department of Oral and Maxillofacial Diseases, University of Helsinki, Helsinki 00014, Finland; Orthodontics, Department of Oral and Maxillofacial Diseases, Helsinki University Hospital, Helsinki 00290, Finland.
  • Noble A; MRC & Asthma UK Centre in Allergic Mechanisms of Asthma, King's College London, United Kingdom.
  • Tucker AS; Department of Craniofacial Development and Stem Cell Biology, Guy's Hospital, King's College London, United Kingdom. Electronic address: abigail.tucker@kcl.ac.uk.
Dev Biol ; 419(2): 348-356, 2016 11 15.
Article en En | MEDLINE | ID: mdl-27590203
Hypertrophy, hyperplasia and altered mucus secretion from the respiratory submucosal glands (SMG) are characteristics of airway diseases such as cystic fibrosis, asthma and chronic bronchitis. More commonly, hyper-secretion of the nasal SMGs contributes to allergic rhinitis and upper airway infection. Considering the role of these glands in disease states, there is a significant dearth in understanding the molecular signals that regulate SMG development and patterning. Due to the imperative role of FGF signalling during the development of other branched structures, we investigated the role of Fgf10 during initiation and branching morphogenesis of murine nasal SMGs. Fgf10 is expressed in the mesenchyme around developing SMGs while expression of its receptor Fgfr2 is seen within glandular epithelial cells. In the Fgf10 null embryo, Steno's gland and the maxillary sinus gland were completely absent while other neighbouring nasal glands showed normal duct elongation but defective branching. Interestingly, the medial nasal glands were present in Fgf10 homozygotes but missing in Fgfr2b mutants, with expression of Fgf7 specifically expressed around these developing glands, indicating that Fgf7 might compensate for loss of Fgf10 in this group of glands. Intriguingly the lateral nasal glands were only mildly affected by loss of FGF signalling, while these glands were missing in Eda mutant mice, where the Steno's and maxillary sinus gland developed as normal. This analysis reveals that regulation of nasal gland development is complex with different subsets of glands being regulated by different signalling pathways. This analysis helps shed light on the nasal gland defects observed in patients with hypohidrotic ectodermal dysplasia (HED) (defect EDA pathway) and LADD syndrome (defect FGFR2b pathway).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos / Factor 10 de Crecimiento de Fibroblastos / Glándulas Exocrinas / Ectodisplasinas Límite: Animals Idioma: En Revista: Dev Biol Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos / Factor 10 de Crecimiento de Fibroblastos / Glándulas Exocrinas / Ectodisplasinas Límite: Animals Idioma: En Revista: Dev Biol Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos