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Identification of a Predominantly Interferon-λ-Induced Transcriptional Profile in Murine Intestinal Epithelial Cells

Type I (α and β) and type III (λ) interferons (IFNs) induce the expression of a large set of antiviral effector molecules via their respective surface membrane receptors. Whereas most cell types respond to type I IFN, type III IFN preferentially acts on epithelial cells and protects mucosal organs s...

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Detalles Bibliográficos
Autores principales: Selvakumar, Tharini A., Bhushal, Sudeep, Kalinke, Ulrich, Wirth, Dagmar, Hauser, Hansjörg, Köster, Mario, Hornef, Mathias W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650613/
https://www.ncbi.nlm.nih.gov/pubmed/29085367
http://dx.doi.org/10.3389/fimmu.2017.01302
Descripción
Sumario:Type I (α and β) and type III (λ) interferons (IFNs) induce the expression of a large set of antiviral effector molecules via their respective surface membrane receptors. Whereas most cell types respond to type I IFN, type III IFN preferentially acts on epithelial cells and protects mucosal organs such as the lung and gastrointestinal tract. Despite the engagement of different receptor molecules, the type I and type III IFN-induced signaling cascade and upregulated gene profile is thought to be largely identical. Here, we comparatively analyzed the response of gut epithelial cells to IFN-β and IFN-λ(2) and identified a set of genes predominantly induced by IFN-λ(2). We confirm the influence of epithelial cell polarization for enhanced type III receptor expression and demonstrate the induction of predominantly IFN-λ(2)-induced genes in the gut epithelium in vivo. Our results suggest that IFN-λ(2) targets the epithelium and induces genes to adjust the antiviral host response to the requirements at mucosal body sites.