S'abonner

Pharmacologic inhibition of Notch signaling suppresses food antigen–induced mucosal mast cell hyperplasia - 19/04/17

Doi : 10.1016/j.jaci.2016.05.046 
Asuka Honjo, MD a, Nobuhiro Nakano, PhD b, , Susumu Yamazaki, MD, PhD a, Mutsuko Hara, PhD b, Koichiro Uchida, MD, PhD b, Jiro Kitaura, MD, PhD b, Chiharu Nishiyama, PhD b, c, Hideo Yagita, PhD d, Yoshikazu Ohtsuka, MD, PhD a, Hideoki Ogawa, MD, PhD b, Ko Okumura, MD, PhD b, Toshiaki Shimizu, MD, PhD a
a Department of Pediatrics and Adolescent Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan 
b Atopy (Allergy) Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan 
c Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University of Science, Tokyo, Japan 
d Department of Immunology, Juntendo University School of Medicine, Tokyo, Japan 

Corresponding author: Nobuhiro Nakano, PhD, Atopy (Allergy) Research Center, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.Atopy (Allergy) Research CenterJuntendo University Graduate School of MedicineTokyo113-8421Japan

Abstract

Background

Mucosal mast cells (MMCs) play a central role in the development of symptoms associated with IgE-mediated food allergy. Recently, Notch2-mediated signaling was shown to be involved in proper MMC distribution in the intestinal tract.

Objective

This study aimed to clarify the mechanism by which Notch signaling regulates MMC distribution in the intestinal mucosa. Furthermore, pharmacologic inhibition of Notch signaling was evaluated as a treatment for symptoms associated with experimental food allergy.

Methods

Bone marrow–derived mast cells generated from mice were cultured with Notch ligands, and then expression of genes associated with MMCs was measured in the cells. In addition, the effect of an inhibitor of Notch signaling on food antigen–induced allergic reactions was examined in a mouse model of food allergy.

Results

Notch signaling induced MMC differentiation through upregulation of expression of genes characteristic of MMCs in the presence of IL-3. Some lamina propria cells isolated from the mouse small intestine expressed Notch ligands and were able to upregulate MMC markers in bone marrow–derived mast cells through Notch signaling. In a mouse model of food allergy, administration of a Notch signaling inhibitor led to suppression of food antigen–induced hyperplasia of intestinal MMCs, resulting in alleviation of allergic diarrhea and systemic anaphylaxis.

Conclusion

Notch signaling contributes to differentiation and accumulation of MMCs in the intestinal mucosa. Thus inhibition of Notch signaling alleviates symptoms associated with experimental food allergy. These results raise the possibility that Notch signaling in mast cells is a novel target for therapy in patients with food allergy.

Le texte complet de cet article est disponible en PDF.

Key words : Notch signaling, mucosal mast cells, food allergy, mast cell hyperplasia

Abbreviations used : BMMC, CHO, CTMC, DAPT, Dll1, Dll4, IQDMA, Jag1, Jag2, LP, MLN, MMC, mMCP, OVA, PE, SCF, STAT5, TLR4


Plan


 Supported in part by MEXT KAKENHI grant no. 15K09784 and the MEXT-Supported Program for the Strategic Research Foundation at Private Universities, 2011-2015, from the Ministry of Education, Culture, Sports, Science and Technology, Japan.
 Disclosure of potential conflict of interest: N. Nakano receives grant support from the Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT KAKENHI grant no. 15K09784) and the MEXT-Supported Program for the Strategic Research Foundation at Private Universities. The rest of the authors declare that they have no relevant conflicts of interest.


© 2016  American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 139 - N° 3

P. 987 - mars 2017 Retour au numéro
Article précédent Article précédent
  • Airborne dust and high temperatures are risk factors for invasive bacterial disease
  • Jean-François Jusot, Daniel R. Neill, Elaine M. Waters, Mathieu Bangert, Marisol Collins, Laura Bricio Moreno, Katiellou G. Lawan, Mouhaiminou Moussa Moussa, Emma Dearing, Dean B. Everett, Jean-Marc Collard, Aras Kadioglu
| Article suivant Article suivant
  • Defective natural killer cell activity in a mouse model of eczema herpeticum
  • Yuko Kawakami, Tomoaki Ando, Jong-Rok Lee, Gisen Kim, Yu Kawakami, Tae Nakasaki, Manando Nakasaki, Kenji Matsumoto, Youn Soo Choi, Toshiaki Kawakami

Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.

Déjà abonné à cette revue ?

Mon compte


Plateformes Elsevier Masson

Déclaration CNIL

EM-CONSULTE.COM est déclaré à la CNIL, déclaration n° 1286925.

En application de la loi nº78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, vous disposez des droits d'opposition (art.26 de la loi), d'accès (art.34 à 38 de la loi), et de rectification (art.36 de la loi) des données vous concernant. Ainsi, vous pouvez exiger que soient rectifiées, complétées, clarifiées, mises à jour ou effacées les informations vous concernant qui sont inexactes, incomplètes, équivoques, périmées ou dont la collecte ou l'utilisation ou la conservation est interdite.
Les informations personnelles concernant les visiteurs de notre site, y compris leur identité, sont confidentielles.
Le responsable du site s'engage sur l'honneur à respecter les conditions légales de confidentialité applicables en France et à ne pas divulguer ces informations à des tiers.


Tout le contenu de ce site: Copyright © 2024 Elsevier, ses concédants de licence et ses contributeurs. Tout les droits sont réservés, y compris ceux relatifs à l'exploration de textes et de données, a la formation en IA et aux technologies similaires. Pour tout contenu en libre accès, les conditions de licence Creative Commons s'appliquent.