Development and selection of Valpha l4i NKT cells.
Détails
ID Serval
serval:BIB_C888E109BDFD
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Development and selection of Valpha l4i NKT cells.
Périodique
Current topics in microbiology and immunology
ISSN
0070-217X
Statut éditorial
Publié
Date de publication
2007
Peer-reviewed
Oui
Volume
314
Pages
195-212
Langue
anglais
Notes
Publication types: Journal Article ; Review
Publication Status: ppublish
Publication Status: ppublish
Résumé
Valpha14 invariant natural killer T (Valpha14i NKT) cells are a unique lineage of mouse T cells that share properties with both NK cells and memory T cells. Valpha14i NKT cells recognize CDld-associated glycolipids via a semi-invariant T cell receptor (TCR) composed of an invariant Valpha14-Jalpha 18 chain paired preferentially with a restricted set of TCRbeta chains. During development in the thymus, rare CD4+ CD8+ (DP) cortical thymocytes that successfully rearrange the semi-invariant TCR are directed to the Valpha14i NKT cell lineage via interactions with CD d-associated endogenous glycolipids expressed by other DP thymocytes. As they mature, Valphal4i NKT lineage cells upregulate activation markers such as CD44 and subsequently express NK-related molecules such as NKI.1 and members of the Ly-49 inhibitory receptor family. The developmental program of Valpha l4i NKT cells is critically regulated by a number of signaling cues that have little or no effect on conventional T cell development, such as the Fyn/SAP/SLAM pathway, NFkappaB and T-bet transcription factors, and the cytokine IL-15. The unique developmental requirements of Valphal4i NKT cells may represent a paradigm for other unconventional T cell subsets that are positively selected by agonist ligands expressed on hematopoietic cells.
Mots-clé
Animals, Cell Differentiation/genetics, Cell Differentiation/immunology, Humans, Killer Cells, Natural/cytology, Killer Cells, Natural/immunology, Mice, Signal Transduction, T-Lymphocyte Subsets/cytology, T-Lymphocyte Subsets/immunology
Pubmed
Web of science
Création de la notice
09/02/2010 13:55
Dernière modification de la notice
20/08/2019 15:43