BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis
Détails
ID Serval
serval:BIB_EDF31F9EA9F3
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis
Périodique
Immunity
ISSN
1074-7613 (Print)
Statut éditorial
Publié
Date de publication
05/2000
Volume
12
Numéro
5
Pages
471-81
Notes
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: May
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: May
Résumé
CXCR5, the receptor for B lymphocyte chemoattractant (BLC), is required for normal development of Peyer's patches, inguinal lymph nodes, and splenic follicles. To test the in vivo activity of BLC in isolation of other lymphoid organizers, transgenic mice were generated expressing BLC in the pancreatic islets. In addition to attracting B cells, BLC expression led to development of lymph node-like structures that contained B and T cell zones, high endothelial venules, stromal cells, and the chemokine SLC. Development of these features was strongly dependent on B lymphocytes and on lymphotoxin alpha1beta2 and could be reversed by blocking lymphotoxin alpha1beta2. These findings establish that BLC is sufficient to activate a pathway of events leading to formation of organized lymphoid tissue.
Mots-clé
Animals
B-Lymphocytes/*immunology/pathology
Chemotactic Factors/immunology
Islets of Langerhans/*immunology/pathology
Lymphoid Tissue/immunology/pathology
Lymphotoxin-alpha/*immunology
Mice
Mice, Transgenic
Receptors, Chemokine
Receptors, Cytokine/*immunology
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/01/2008 15:04
Dernière modification de la notice
20/08/2019 16:15