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Projekt Druckansicht

Das Cytokin IL-31, assoziert mit atopischer Dermatitis, kontrolliert die Physiologie von Keratinozyten und die Barrierefunktion der Haut

Fachliche Zuordnung Dermatologie
Förderung Förderung von 2011 bis 2015
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 206858601
 
Erstellungsjahr 2016

Zusammenfassung der Projektergebnisse

Atopic dermatitis, a chronic inflammatory skin disease with increasing prevalence, is closely associated with skin barrier defects. A cytokine related to disease severity and inhibition of keratinocyte differentiation is IL-31. To identify its molecular targets, IL-31-dependent gene expression was determined in this study by using a newly developed 3-D organotypic skin model. IL-31 regulated genes are involved in the formation of an intact physical skin barrier. Many of these genes were poorly induced during differentiation as a consequence of IL-31 treatment, resulting in increased penetrability to allergens and irritants as demonstrated in various novel functional assays. Furthermore studies employing cell-sorted skin equivalents in SCID/NOD mice demonstrated enhanced transepidermal water loss following subcutaneous administration of IL-31. We also identified the IL-1 cytokine network as a downstream effector of IL-31 signaling. Anakinra, an IL-1 receptor antagonist, blocked the IL- 31 effects on skin differentiation. In addition to the effects on the physical barrier, IL-31 stimulated the expression of antimicrobial peptides thereby inhibiting bacterial growth on the 3-dimensional organotypic skin models. This was evident already at low doses of IL-31, insufficient to interfere with the physical barrier. Together these findings demonstrate that IL-31 effects keratinocyte differentiation in multiple ways and that the IL-1 cytokine network is a major downstream effector of IL-31 signaling in deregulating the physical skin barrier. Within this project we were able to describe for the first time the physiological role of IL-31 in healthy human skin and the dose dependent pathological role of IL-31 on various skin barrier structures in AD. In this project were able to discover that the IL-1α pathway is the major pathway responsible for mediating the effect of IL-31 on skin barrier function (not release of IL-20/-24 as suggested in the grant proposal). We also discovered the physiological function of IL-31 regulating the expression of various antimicrobial peptides important for a functional chemical barrier. Untersuchungen aus dem geförderten Projekt wurden mit folgenden Preisen ausgezeichnet: ADF/ECARF (Europäischen Stiftung für Allergieforschung) Award 2013; Mainzer Abstract-Preis der Deutschen Gesellschaft für Allergologie und Klinische Immunologie 2014; Mainzer Abstract-Preis der Deutschen Gesellschaft für Allergologie und Klinische Immunologie 2013; Mainzer Abstract-Preis der Deutschen Gesellschaft für Allergologie und Klinische Immunologie 2012; Research on Skin-Dryness Award 2012 (La Roche-Posay Laboratoire Dermatologique Deutschland); Promotionspreis der Medizinischen Fakultät der RWTH Aachen 2012.

Projektbezogene Publikationen (Auswahl)

 
 

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