| Literature DB >> 25558064 |
Henry Danahay1, Angelica D Pessotti2, Julie Coote3, Brooke E Montgomery2, Donghui Xia2, Aaron Wilson2, Haidi Yang2, Zhao Wang2, Luke Bevan3, Chris Thomas2, Stephanie Petit2, Anne London4, Peter LeMotte4, Arno Doelemeyer5, Germán L Vélez-Reyes2, Paula Bernasconi2, Christy J Fryer2, Matt Edwards3, Paola Capodieci2, Amy Chen2, Marc Hild2, Aron B Jaffe6.
Abstract
The balance and distribution of epithelial cell types is required to maintain tissue homeostasis. A hallmark of airway diseases is epithelial remodeling, leading to increased goblet cell numbers and an overproduction of mucus. In the conducting airway, basal cells act as progenitors for both secretory and ciliated cells. To identify mechanisms regulating basal cell fate, we developed a screenable 3D culture system of airway epithelial morphogenesis. We performed a high-throughput screen using a collection of secreted proteins and identified inflammatory cytokines that specifically biased basal cell differentiation toward a goblet cell fate, culminating in enhanced mucus production. We also demonstrate a specific requirement for Notch2 in cytokine-induced goblet cell metaplasia in vitro and in vivo. We conclude that inhibition of Notch2 prevents goblet cell metaplasia induced by a broad range of stimuli and propose Notch2 neutralization as a therapeutic strategy for preventing goblet cell metaplasia in airway diseases.Entities:
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Year: 2014 PMID: 25558064 DOI: 10.1016/j.celrep.2014.12.017
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423