| dc.contributor |
Ministerio de Economía y Competitividad (España) |
|
| dc.contributor |
Comunidad de Madrid |
|
| dc.contributor |
Obra Social la Caixa |
|
| dc.contributor |
Fundación Eugenio Rodríguez Pascual |
|
| dc.contributor |
Fundación Ramón Areces |
|
| dc.creator |
García-Peydró, Marina |
|
| dc.creator |
Yébenes, Virginia G. de |
|
| dc.creator |
Toribio, María Luisa |
|
| dc.date |
2008-06-10T14:26:53Z |
|
| dc.date |
2008-06-10T14:26:53Z |
|
| dc.date |
2006 |
|
| dc.date.accessioned |
2017-01-31T01:38:43Z |
|
| dc.date.available |
2017-01-31T01:38:43Z |
|
| dc.identifier |
The Journal of Immunology, 2006, 177: 3711-3720 |
|
| dc.identifier |
0022-1767 (Print) |
|
| dc.identifier |
1550-6606 (Online) |
|
| dc.identifier |
http://hdl.handle.net/10261/4960 |
|
| dc.identifier.uri |
http://dspace.mediu.edu.my:8181/xmlui/handle/10261/4960 |
|
| dc.description |
Article available at http://www.jimmunol.org/cgi/content/abstract/177/6/3711 |
|
| dc.description |
Notch signaling is critical for T cell development of multipotent hemopoietic progenitors. Yet, how Notch regulates T cell fate specification during early thymopoiesis remains unclear. In this study, we have identified an early subset of CD34highc-kit+flt3+IL-7R+ cells in the human postnatal thymus, which includes primitive progenitors with combined lymphomyeloid potential. To assess the impact of Notch signaling in early T cell development, we expressed constitutively active Notch1 in such thymic lymphomyeloid precursors (TLMPs), or triggered their endogenous Notch pathway in the OP9-Delta-like1 stroma coculture. Our results show that proliferation vs differentiation is a critical decision influenced by Notch at the TLMP stage. We found that Notch signaling plays a prominent role in inhibiting non-T cell differentiation (i.e., macrophages, dendritic cells, and NK cells) of TLMPs, while sustaining the proliferation of undifferentiated thymocytes with T cell potential in response to unique IL-7 signals. However, Notch activation is not sufficient for inducing T-lineage progression of proliferating progenitors. Rather, stroma-derived signals are concurrently required. Moreover, while ectopic IL-7R expression cannot replace Notch for the maintenance and expansion of undifferentiated thymocytes, Notch signals sustain IL-7R expression in proliferating thymocytes and induce IL-7R up-regulation in a T cell line. Thus, IL-7R and Notch pathways cooperate to synchronize cell proliferation and suppression of non-T lineage choices in primitive intrathymic progenitors, which will be allowed to progress along the T cell pathway only upon interaction with an inductive stromal microenvironment. These data provide insight into a mechanism of Notch-regulated amplification of the intrathymic pool of early human T cell progenitors |
|
| dc.description |
This work was supported by grants from Plan Nacional de Biomedicina (SAF2004-01122 and GEN2003-20649-C06-02), Comunidad de Madrid (GR/SAL/0143/ 2004), Fundación La Caixa (ON03/109-00), and Fundación Eugenio Rodríguez Pascual. We thank the Fundación Ramón Areces for an institutional grant to the Centro de Biología Molecular Severo Ochoa |
|
| dc.description |
Peer reviewed |
|
| dc.format |
664838 bytes |
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| dc.format |
application/pdf |
|
| dc.language |
eng |
|
| dc.publisher |
American Association of Immunologists |
|
| dc.rights |
openAccess |
|
| dc.subject |
Human |
|
| dc.subject |
T cells |
|
| dc.subject |
Cell proliferation |
|
| dc.subject |
Hematopoiesis |
|
| dc.subject |
Thymus |
|
| dc.title |
Notch1 and IL-7 Receptor Interplay Maintains Proliferation of Human Thymic Progenitors while Suppressing Non-T Cell Fates |
|
| dc.type |
Artículo |
|