Atopic dermatitis-like disease and associated lethal myeloproliferative disorder arise from loss of Notch signaling in the murine skin.
Détails
Télécharger: BIB_BF783DDCBA05.P001.pdf (4267.89 [Ko])
Etat: Public
Version: de l'auteur⸱e
Etat: Public
Version: de l'auteur⸱e
ID Serval
serval:BIB_BF783DDCBA05
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Atopic dermatitis-like disease and associated lethal myeloproliferative disorder arise from loss of Notch signaling in the murine skin.
Périodique
PLoS One
ISSN
1932-6203[electronic], 1932-6203[linking]
Statut éditorial
Publié
Date de publication
2010
Volume
5
Numéro
2
Pages
e9258
Langue
anglais
Résumé
BACKGROUND: The Notch pathway is essential for proper epidermal differentiation during embryonic skin development. Moreover, skin specific loss of Notch signaling in the embryo results in skin barrier defects accompanied by a B-lymphoproliferative disease. However, much less is known about the consequences of loss of Notch signaling after birth. METHODOLOGY AND PRINCIPAL FINDINGS: To study the function of Notch signaling in the skin of adult mice, we made use of a series of conditional gene targeted mice that allow inactivation of several components of the Notch signaling pathway specifically in the skin. We demonstrate that skin-specific inactivation of Notch1 and Notch2 simultaneously, or RBP-J, induces the development of a severe form of atopic dermatitis (AD), characterized by acanthosis, spongiosis and hyperkeratosis, as well as a massive dermal infiltration of eosinophils and mast cells. Likewise, patients suffering from AD, but not psoriasis or lichen planus, have a marked reduction of Notch receptor expression in the skin. Loss of Notch in keratinocytes induces the production of thymic stromal lymphopoietin (TSLP), a cytokine deeply implicated in the pathogenesis of AD. The AD-like associated inflammation is accompanied by a myeloproliferative disorder (MPD) characterized by an increase in immature myeloid populations in the bone marrow and spleen. Transplantation studies revealed that the MPD is cell non-autonomous and caused by dramatic microenvironmental alterations. Genetic studies demontrated that G-CSF mediates the MPD as well as changes in the bone marrow microenvironment leading to osteopenia. SIGNIFICANCE: Our data demonstrate a critical role for Notch in repressing TSLP production in keratinocytes, thereby maintaining integrity of the skin and the hematopoietic system.
Mots-clé
Animals, Cytokines/metabolism, Dermatitis, Atopic/genetics, Dermatitis, Atopic/mortality, Flow Cytometry, Granulocyte Colony-Stimulating Factor/genetics, Granulocyte Colony-Stimulating Factor/metabolism, Humans, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Nude, Mice, Transgenic, Models, Biological, Myeloproliferative Disorders/genetics, Myeloproliferative Disorders/mortality, Receptor, Notch1/genetics, Receptor, Notch1/physiology, Receptor, Notch2/genetics, Receptor, Notch2/physiology, Receptors, Cytokine/genetics, Receptors, Cytokine/metabolism, Receptors, Notch/genetics, Receptors, Notch/physiology, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction/genetics, Signal Transduction/physiology, Skin/metabolism, Skin/pathology, Survival Analysis, Survival Rate
Pubmed
Web of science
Open Access
Oui
Création de la notice
09/03/2010 11:50
Dernière modification de la notice
20/08/2019 15:33