Abstract
We have analyzed the roles of Notch and IL-7 signaling in the proliferation and differentiation of mouse progenitor thymocyte subpopulations cultured on Notch delta-like-1 ligand-expressing OP9 stromal cells. Using bulk and limiting dilution cultures, we show that DN1 and DN2 cells require both Notch and IL-7 signaling for efficient proliferation and differentiation into cytoplasmic TCRβ and surface TCRα/β and TCRγ/δ expressing T cells. Selection for cytoplasmic TCRβ-positive cells is dependent on preTα expression. Both γ/δ and α/β TCR expressing T cells arising in culture can be efficiently stimulated by anti-CD3 cross-linking, suggesting that they might be functional. The differentiation of adult, but not fetal, DN1 and DN2 thymocytes into CD4 and/or CD8 expressing cells is inhibited by IL-7. Finally, efficient proliferation and differentiation of DN3 cells requires Notch signaling and preTCR expression, but is independent of IL-7.
| Original language | English |
|---|---|
| Pages (from-to) | 1292-1300 |
| Number of pages | 9 |
| Journal | European Journal of Immunology |
| Volume | 35 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Apr 2005 |
| Externally published | Yes |
Keywords
- IL-7
- Lymphopoiesis
- Notch
- PreTCR
- Progenitor cells