BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis

Details

Serval ID
serval:BIB_EDF31F9EA9F3
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
BLC expression in pancreatic islets causes B cell recruitment and lymphotoxin-dependent lymphoid neogenesis
Journal
Immunity
Author(s)
Luther  S. A., Lopez  T., Bai  W., Hanahan  D., Cyster  J. G.
ISSN
1074-7613 (Print)
Publication state
Published
Issued date
05/2000
Volume
12
Number
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
Abstract
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.
Keywords
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
Yes
Create date
24/01/2008 15:04
Last modification date
20/08/2019 16:15
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