Crosstalk between NOTCH and AKT signaling during murine megakaryocyte lineage specification

被引:60
作者
Cornejo, Melanie G. [2 ]
Mabialah, Vinciane [3 ]
Sykes, Stephen M. [2 ]
Khandan, Tulasi [2 ]
Lo Celso, Cristina [4 ]
Lopez, Cecile K. [3 ]
Rivera-Munoz, Paola [3 ]
Rameau, Philippe
Tothova, Zuzana [2 ]
Aster, Jon C. [5 ]
DePinho, Ronald A. [6 ,7 ]
Scadden, David T. [4 ]
Gilliland, D. Gary [2 ]
Mercher, Thomas [1 ,2 ,3 ]
机构
[1] Inst Gustave Roussy, INSERM, U985, F-94800 Villejuif, France
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Hematol,Dept Med, Boston, MA 02115 USA
[3] Univ Paris 11, INSERM, U985, Villejuif, France
[4] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[5] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Pathol,Dept Med, Boston, MA 02115 USA
[6] Dana Farber Canc Inst, Belfer Inst Appl Canc Sci, Dept Med Oncol, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Dept Med & Genet, Boston, MA USA
关键词
HEMATOPOIETIC STEM-CELLS; FOXO TRANSCRIPTION FACTORS; SELF-RENEWAL; IN-VIVO; LEUKEMIA; PATHWAYS; PROGENITORS; PTEN; THROMBOPOIETIN; IDENTIFICATION;
D O I
10.1182/blood-2011-01-328567
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The NOTCH signaling pathway is implicated in a broad range of developmental processes, including cell fate decisions. However, the molecular basis for its role at the different steps of stem cell lineage commitment is unclear. We recently identified the NOTCH signaling pathway as a positive regulator of megakaryocyte lineage specification during hematopoiesis, but the developmental pathways that allow hematopoietic stem cell differentiation into the erythro-megakaryocytic lineages remain controversial. Here, we investigated the role of downstream mediators of NOTCH during megakaryopoiesis and report crosstalk between the NOTCH and PI3K/AKT pathways. We demonstrate the inhibitory role of phosphatase with tensin homolog and Forkhead Box class O factors on megakaryopoiesis in vivo. Finally, our data annotate developmental mechanisms in the hematopoietic system that enable a decision to be made either at the hematopoietic stem cell or the committed progenitor level to commit to the megakaryocyte lineage, supporting the existence of 2 distinct developmental pathways. (Blood. 2011;118(5):1264-1273)
引用
收藏
页码:1264 / 1273
页数:10
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