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Ectodysplasin and Wnt pathways are required for salivary gland branching morphogenesis

Item Type:Article
Title:Ectodysplasin and Wnt pathways are required for salivary gland branching morphogenesis
Creators Name:Haeaerae, O., Fujimori, S., Schmidt-Ullrich, R., Hartmann, C., Thesleff, I. and Mikkola, M.L.
Abstract:The developing submandibular salivary gland (SMG) is a well-studied model for tissue interactions and branching morphogenesis. Its development shares similar features with other ectodermal appendages such as hair and tooth. The ectodysplasin (Eda) pathway is essential for the formation and function of several ectodermal organs. Mutations in the signaling components of the Eda pathway lead to a human syndrome known as hypohidrotic ectodermal dysplasia (HED), which is characterized by missing and malformed teeth, sparse hair and reduced sweating. Individuals with HED suffer also from dry mouth because of reduced saliva flow. In order to understand the underlying mechanism, we analyzed salivary gland development in mouse models with altered Eda pathway activities. We have found that Eda regulates growth and branching of the SMG via transcription factor NF-{kappa}B in the epithelium, and that the hedgehog pathway is an important mediator of Eda/NF-{kappa}B. We also sought to determine whether a similar reciprocal interplay between the Eda and Wnt/{beta}-catenin pathways, which are known to operate in other skin appendages, functions in developing SMG. Surprisingly and unlike in developing hair follicles and teeth, canonical Wnt signaling activity did not colocalize with Edar/NF-{kappa}B in salivary gland epithelium. Instead, we observed high mesenchymal Wnt activity and show that ablation of mesenchymal Wnt signaling either in vitro or in vivo compromised branching morphogenesis. We also provide evidence suggesting that the effects of mesenchymal Wnt/{beta}-catenin signaling are mediated, at least in part, through regulation of Eda expression.
Keywords:Tabby, Ectodysplasin, Edar, Salivary Gland, HED, Branching Morphogenesis, NF-kappaB, Wnt, Sonic Hedgehog, Animals, Mice
Source:Development
ISSN:0950-1991
Publisher:Company of Biologists
Volume:138
Number:13
Page Range:2681-2691
Date:July 2011
Official Publication:https://doi.org/10.1242/dev.057711
PubMed:View item in PubMed

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