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Sustained Expression of Pre-TCR Induced β-Catenin in Post-β-Selection Thymocytes Blocks T Cell Development
- Source :
- The Journal of Immunology. 182:759-765
- Publication Year :
- 2009
- Publisher :
- The American Association of Immunologists, 2009.
-
Abstract
- Pre-TCR and IL-7R signals regulate β-selection of thymocytes and then must be down-regulated for further development. However, the molecular events that control down-regulation remain unknown. We and others have previously shown that β-catenin in cooperation with TCF regulates β-selection. In this paper, we demonstrate that β-catenin expression is stringently regulated by intrathymic signals, it is expressed at the highest levels in the pre-TCR signaled thymocytes, and is down-regulated in post-β-selection thymocytes. Pre-TCR-induced β-catenin regulates initial stages of pre-TCR signaling including expression of early growth response (Egr) genes but must be down-regulated to express RORγt, which is essential for maturation to the CD4+CD8+ double positive (DP) stage. Sustained expression of β-catenin results in the generation of IL-7R-, Egr-, and TGFβ-expressing pre-DP thymocytes that are blocked in development. These data are consistent with a model in which post-β-selection, pre-TCR-induced β-catenin expression must return to background levels for efficient transition to the DP stage.
- Subjects :
- CD4-Positive T-Lymphocytes
medicine.medical_specialty
Time Factors
Receptors, Antigen, T-Cell, alpha-beta
Cellular differentiation
T cell
Immunology
Double negative
Down-Regulation
Mice, Transgenic
Thymus Gland
CD8-Positive T-Lymphocytes
Biology
Article
Mice
T-Lymphocyte Subsets
RAR-related orphan receptor gamma
Internal medicine
medicine
Animals
Immunology and Allergy
Gene Rearrangement, beta-Chain T-Cell Antigen Receptor
Protein Precursors
beta Catenin
Mice, Knockout
Cell Cycle
T-cell receptor
Cell Differentiation
Cell cycle
Growth Inhibitors
Cell biology
Mice, Inbred C57BL
medicine.anatomical_structure
Endocrinology
Catenin
CD8
Subjects
Details
- ISSN :
- 15506606 and 00221767
- Volume :
- 182
- Database :
- OpenAIRE
- Journal :
- The Journal of Immunology
- Accession number :
- edsair.doi.dedup.....2460446a8701b90e37b4f8d422e457db
- Full Text :
- https://doi.org/10.4049/jimmunol.182.2.759