Identification of renin progenitors in the mouse bone marrow that give rise to B-cell leukaemia

被引:28
作者
Belyea, Brian C. [1 ]
Xu, Fang [1 ]
Pentz, Ellen S. [1 ]
Medrano, Silvia [1 ]
Li, Minghong [1 ]
Hu, Yan [1 ]
Turner, Stephen [2 ]
Legallo, Robin [3 ]
Jones, Craig A. [4 ]
Tario, Joseph D. [4 ]
Liang, Ping [5 ]
Gross, Kenneth W. [4 ]
Sequeira-Lopez, Maria Luisa S. [1 ]
Gomez, R. Ariel [1 ]
机构
[1] Univ Virginia, Sch Med, Dept Pediat, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Bioinformat, Charlottesville, VA 22908 USA
[3] Univ Virginia, Sch Med, Dept Pathol, Charlottesville, VA 22908 USA
[4] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[5] Brock Univ, Dept Biol Sci, St Catharines, ON L2S 3A1, Canada
基金
美国国家卫生研究院;
关键词
HEMATOPOIETIC STEM-CELLS; ANGIOTENSIN SYSTEM; GENE-EXPRESSION; DEVELOPING KIDNEY; MYELOID-LEUKEMIA; REVEALS; MICE; IDENTITY; LINEAGE; PROGRESSION;
D O I
10.1038/ncomms4273
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The cell of origin and triggering events for leukaemia are mostly unknown. Here we show that the bone marrow contains a progenitor that expresses renin throughout development and possesses a B-lymphocyte pedigree. This cell requires RBP-J to differentiate. Deletion of RBP-J in these renin-expressing progenitors enriches the precursor B-cell gene programme and constrains lymphocyte differentiation, facilitated by H3K4me3 activating marks in genes that control the pre-B stage. Mutant cells undergo neoplastic transformation, and mice develop a highly penetrant B-cell leukaemia with multi-organ infiltration and early death. These reninexpressing cells appear uniquely vulnerable as other conditional models of RBP-J deletion do not result in leukaemia. The discovery of these unique renin progenitors in the bone marrow and the model of leukaemia described herein may enhance our understanding of normal and neoplastic haematopoiesis.
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页数:14
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