Abstract
The suggested role of Notch1 or its mutants in thymocyte differentiation and T cell tumorigenesis raises the question of how the different members of the Notch family influence distinct steps in T cell development and the role played by Notch ligands in the thymus. We report here that different Notch receptor-ligand partnerships may occur inside the thymus, as we observed differential expression of Notch1, 2 and 3 receptors, their ligands Jagged1 and 2, and downstream intracellular effectors hairy and Enhancer of Split homolog 1 (HES-1) and hairy and Enhancer of Split homolog 5 (HES-5), depending on ontogenetic stage and thymic cell populations. Indeed, while Jagged2 is expressed in both stromal cells and thymocytes, Jagged1 expression is restricted to stromal cells. Moreover, a differential distribution of Notch3, with respect to Notch1, was observed in distinct age-related thymocyte subsets. Finally, Notch3 was preferentially up-regulated in thymocytes, following the induction of their differentiation by interaction with thymic epithelial cells expressing the cognate Jagged1 and 2 ligands, suggesting that, besides Notch1, Notch3 may also be involved in distinct steps of thymocyte development. Our results suggest that the Notch signaling pathway is involved in a complex interplay of T cell developmental stages, as a consequence of the heterogeneity and specific expression of members of the Notch receptor family and their cognate ligands, in distinct thymic cell compartments.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Basic Helix-Loop-Helix Transcription Factors
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Calcium-Binding Proteins
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Carrier Proteins / biosynthesis
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Carrier Proteins / metabolism
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Carrier Proteins / physiology*
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Cell Differentiation / immunology
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DNA-Binding Proteins / biosynthesis
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Helix-Loop-Helix Motifs
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Homeodomain Proteins / biosynthesis
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Intercellular Signaling Peptides and Proteins
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Jagged-1 Protein
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Jagged-2 Protein
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Ligands
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Lymphoid Tissue / cytology
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Lymphoid Tissue / metabolism
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Male
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Membrane Proteins / biosynthesis
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Membrane Proteins / metabolism
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Membrane Proteins / physiology*
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Mice
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Mice, Inbred C57BL
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Protein Biosynthesis
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Proteins / metabolism
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Proteins / physiology*
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Proto-Oncogene Proteins / biosynthesis
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Proto-Oncogene Proteins / metabolism
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Proto-Oncogene Proteins / physiology
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RNA, Messenger / biosynthesis
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RNA, Messenger / metabolism
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Receptor, Notch1
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Receptor, Notch2
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Receptor, Notch3
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Receptor, Notch4
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Receptors, Cell Surface / biosynthesis
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Receptors, Cell Surface / metabolism
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Receptors, Cell Surface / physiology*
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Receptors, Notch
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Repressor Proteins / biosynthesis
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Serrate-Jagged Proteins
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Signal Transduction / immunology
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Stromal Cells / metabolism
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T-Lymphocyte Subsets / cytology
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T-Lymphocytes / cytology*
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T-Lymphocytes / metabolism
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Thymus Gland / cytology*
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Thymus Gland / metabolism*
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Transcription Factor HES-1
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Transcription Factors*
Substances
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Basic Helix-Loop-Helix Transcription Factors
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Calcium-Binding Proteins
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Carrier Proteins
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DNA-Binding Proteins
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Hes1 protein, mouse
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Hes5 protein, mouse
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Homeodomain Proteins
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Intercellular Signaling Peptides and Proteins
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JAG1 protein, human
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JAG2 protein, human
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Jag1 protein, mouse
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Jag2 protein, mouse
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Jagged-1 Protein
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Jagged-2 Protein
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Ligands
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Membrane Proteins
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Notch1 protein, mouse
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Notch2 protein, mouse
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Notch3 protein, mouse
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Proteins
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Proto-Oncogene Proteins
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RNA, Messenger
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Receptor, Notch1
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Receptor, Notch2
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Receptor, Notch3
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Receptor, Notch4
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Receptors, Cell Surface
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Receptors, Notch
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Repressor Proteins
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Serrate-Jagged Proteins
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Transcription Factor HES-1
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Transcription Factors
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Notch4 protein, mouse
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HES5 protein, human