Instruction of distinct CD4 T helper cell fates by different notch ligands on antigen-presenting cells.

TitleInstruction of distinct CD4 T helper cell fates by different notch ligands on antigen-presenting cells.
Publication TypeJournal Article
Year of Publication2004
AuthorsAmsen, D, J Blander, M, Lee, GRyol, Tanigaki, K, Honjo, T, Flavell, RA
JournalCell
Volume117
Issue4
Pagination515-26
Date Published2004 May 14
ISSN0092-8674
KeywordsAnimals, Antigen-Presenting Cells, Calcium-Binding Proteins, Cell Differentiation, Cell Lineage, DNA-Binding Proteins, GATA3 Transcription Factor, Immunoglobulin J Recombination Signal Sequence-Binding Protein, Intercellular Signaling Peptides and Proteins, Interleukin-4, Intracellular Signaling Peptides and Proteins, Jagged-1 Protein, Membrane Proteins, Mice, Mice, Transgenic, Nuclear Proteins, Receptor, Notch1, Receptors, Cell Surface, Serrate-Jagged Proteins, T-Lymphocytes, Helper-Inducer, Th1 Cells, Th2 Cells, Trans-Activators, Transcription Factors
Abstract

Antigen-presenting cells (APC) tailor immune responses to microbial encounters by stimulating differentiation of CD4 T cells into the Th1 and Th2 lineages. We demonstrate that APC use the Notch pathway to instruct T cell differentiation. Strikingly, of the two Notch ligand families, Delta induces Th1, while Jagged induces the alternate Th2 fate. Expression of these different Notch ligands on APC is induced by Th1- or Th2-promoting stimuli. Th2 differentiation has been considered a default process as APC-derived instructive signals are unknown. We demonstrate that Jagged constitutes an instructive signal for Th2 differentiation, which is independent of IL4/STAT6. Th2 differentiation induced by APC is abrogated in T cells lacking the Notch effector RBPJkappa. Notch directs Th2 differentiation by inducing GATA3 and by directly regulating il4 gene transcription through RBPJkappa sites in a 3' enhancer.

Alternate JournalCell
PubMed ID15137944