| Literature DB >> 15100261 |
Maria Ciofani1, Thomas M Schmitt, Amelia Ciofani, Alison M Michie, Nicolas Cuburu, Anne Aublin, Janet L Maryanski, Juan Carlos Zúñiga-Pflücker.
Abstract
The first checkpoint during T cell development, known as beta selection, requires the successful rearrangement of the TCR-beta gene locus. Notch signaling has been implicated in various stages during T lymphopoiesis. However, it is unclear whether Notch receptor-ligand interactions are necessary during beta selection. Here, we show that pre-TCR signaling concurrent with Notch receptor and Delta-like-1 ligand interactions are required for the survival, proliferation, and differentiation of mouse CD4(-)CD8(-) thymocytes to the CD4(+)CD8(+) stage. Furthermore, we address the minimal signaling requirements underlying beta selection and show a hierarchical positioning of key proximal signaling molecules. Collectively, our results demonstrate an essential role for Notch receptor-ligand interactions in enabling the autonomous signaling capacity of the pre-TCR complex.Entities:
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Year: 2004 PMID: 15100261 DOI: 10.4049/jimmunol.172.9.5230
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422