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Obligatory Role for Cooperative Signaling by Pre-TCR and Notch during Thymocyte Differentiation
Author(s) -
Maria Ciofani,
Thomas M. Schmitt,
Amelia Ciofani,
Alison M. Michie,
Nicolas Çuburu,
Anne Aublin,
Janet L. Maryanski,
Juan Carlos ZúñigaPflücker
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.172.9.5230
Subject(s) - notch signaling pathway , t cell receptor , thymocyte , cd8 , microbiology and biotechnology , biology , lymphopoiesis , signal transduction , receptor , hes3 signaling axis , t cell , immunology , haematopoiesis , genetics , immune system , stem cell
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.

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