| First Author | Wong GW | Year | 2012 |
| Journal | Blood | Volume | 120 |
| Issue | 7 | Pages | 1439-48 |
| PubMed ID | 22649105 | Mgi Jnum | J:189112 |
| Mgi Id | MGI:5444357 | Doi | 10.1182/blood-2011-12-395319 |
| Citation | Wong GW, et al. (2012) HES1 opposes a PTEN-dependent check on survival, differentiation, and proliferation of TCRbeta-selected mouse thymocytes. Blood 120(7):1439-48 |
| abstractText | The developmental progression of immature thymocytes requires cooperative input from several pathways, with Notch signals playing an indispensable role at the T-cell receptor (TCR)-beta selection checkpoint. Notch signals affect the activation of the PI3K/Akt pathway, which is required for pTalpha/TCRbeta (pre-TCR)-induced survival, differentiation, and proliferation of developing alphabeta-lineage thymocytes. However, the molecular players responsible for the interaction between the Notch and PI3K pathways at this critical developmental stage are unknown. Here, we show that Notch induction of Hes1 is necessary to repress the PI3K/Akt pathway inhibitor, PTEN (phosphatase and tensin homolog), which in turn facilitates pre-TCR-induced differentiation. In support of this mechanism, deletion or down-regulation of Pten overcomes the Notch signaling requirement for survival and differentiation during beta-selection. In addition, c-Myc is a critical target of Notch at this stage, as c-Myc expression overcomes the Notch signaling requirement for proliferation during beta-selection. Collectively, our results point to HES1, via repression of PTEN, and c-Myc as critical mediators of Notch function at the beta-selection checkpoint. |
