CD4+CD3- cells induce Peyer's patch development: role of alpha4beta1 integrin activation by CXCR5.

Détails

ID Serval
serval:BIB_F466B252CBDD
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
CD4+CD3- cells induce Peyer's patch development: role of alpha4beta1 integrin activation by CXCR5.
Périodique
Immunity
Auteur⸱e⸱s
Finke D., Acha-Orbea H., Mattis A., Lipp M., Kraehenbuhl J.
ISSN
1074-7613 (Print)
ISSN-L
1074-7613
Statut éditorial
Publié
Date de publication
2002
Volume
17
Numéro
3
Pages
363-373
Langue
anglais
Résumé
CD4+CD3- cells are the predominant hematopoietic cells found in mouse fetal intestine. We prove their role as Peyer's patch (PP)-inducing cells by transfer into neonatal PP-deficient mice. To test the requirement of chemokines and adhesion molecules in induction of PP, we studied mice deficient in CXCR5 and/or alpha4beta1 integrin-mediated adhesion. CXCR5-/- mice have CD4+CD3- cells, which are inefficient in inducing PP formation. We show here that CXCR5/CXCL13 signaling activates alpha4beta1 integrin on CD4+CD3- cells. Blocking of beta1 integrin or VCAM-1, the ligand of alpha4beta1 integrin, inhibits PP formation. This study demonstrates the link between chemokine receptors and adhesion molecules that regulates stromal/hematopoietic cell interaction leading to PP formation.
Mots-clé
Adoptive Transfer, Animals, Antigens, CD3/analysis, CD4-Positive T-Lymphocytes/physiology, CD4-Positive T-Lymphocytes/transplantation, Cell Adhesion, Chemokine CXCL13, Chemokines, CXC/physiology, Immunologic Deficiency Syndromes/genetics, Immunologic Deficiency Syndromes/immunology, Integrin alpha4beta1/physiology, Mice, Mice, Inbred C57BL, Mice, Knockout, Models, Immunological, Morphogenesis, Peyer's Patches/growth &amp, development, Radiation Chimera, Receptors, CXCR5, Receptors, Chemokine, Receptors, Cytokine/deficiency, Receptors, Cytokine/genetics, Signal Transduction/immunology, Stromal Cells/cytology, Vascular Cell Adhesion Molecule-1/physiology
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/01/2008 15:48
Dernière modification de la notice
20/08/2019 17:21
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