Αρχειοθήκη ιστολογίου

Αλέξανδρος Γ. Σφακιανάκης
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5
Άγιος Νικόλαος Κρήτη 72100
2841026182
6032607174

Παρασκευή 3 Μαρτίου 2017

MicroRNA-155 is a critical regulator of type 2 innate lymphoid cells and IL-33 signaling in experimental models of allergic airway inflammation

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Publication date: March 2017
Source:Journal of Allergy and Clinical Immunology, Volume 139, Issue 3
Author(s): Kristina Johansson, Carina Malmhäll, Patricia Ramos-Ramírez, Madeleine Rådinger
BackgroundAllergic airway inflammation is triggered by allergen exposure through several steps including release of IL-33, which promotes cytokine (IL-5, IL-13) production by type 2 innate lymphoid cells (ILC2s). MicroRNA (miR)-155 has recently been described to regulate adaptive responses in allergic inflammation. However, the role of miR-155 in the regulation of ILC2s remains unexplored.ObjectiveWe sought to elucidate the contribution of miR-155 in ILC2 expansion using experimental murine models of allergic airway inflammation.MethodsTo determine the role of miR-155 in the regulation of ILC2s in allergic airway inflammation, miR-155 deficient (miR-155−/−) and wild-type (WT) mice were subjected to acute or chronic allergen-induced inflammation or treated with recombinant IL-33.ResultsmiR-155 was 10-fold upregulated in WT-derived ILC2s in response to IL-33. Furthermore, miR-155−/− mice demonstrated impaired lung IL-33 levels in response to allergen challenge and the number of ILC2s was significantly reduced in allergen-challenged miR-155−/− mice compared with WT mice. Exogenous IL-33 treatment revealed that miR-155 is needed for IL-33–induced ILC2 expansion and eosinophilic airway inflammation. Indeed, ILC2s from IL-33–challenged miR-155−/− lungs exhibited impaired proliferation, GATA-3 expression, and IL-13 production as compared with IL-33–challenged WT ILC2s.ConclusionsOur findings for the first time demonstrate that ILC2s and IL-33 signaling are regulated by miR-155 in allergic airway inflammation.



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