Enforced expression of EBF in hematopoietic stem cells restricts lymphopoiesis to the B cell lineage

被引:64
作者
Zhang, Z
Cotta, CV
Stephan, RP
deGuzman, CG
Klug, CA [1 ]
机构
[1] Univ Alabama Birmingham, Dept Microbiol, Div Dev & Clin Immunol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Dept Human Genet, Birmingham, AL 35294 USA
关键词
B cell development; EBF; hematopoietic stem cell; T cell development; transcription factor;
D O I
10.1093/emboj/cdg464
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mice deficient in early B cell factor (EBF) are blocked at the progenitor B cell stage prior to immunoglobulin gene rearrangement. The EBF-dependent block in B cell development occurs near the onset of B-lineage commitment, which raises the possibility that EBF may act instructively to specify the B cell fate from uncommitted, multipotential progenitor cells. To test this hypothesis, we transduced enriched hematopoietic progenitor cells with a retroviral vector that coexpressed EBF and the green fluorescent protein (GFP). Mice reconstituted with EBF-expressing cells showed a near complete absence of T lymphocytes. Spleen and peripheral blood samples were >95 and 90% GFP(+)EBF(+) mature B cells, respectively. Both NK and lymphoid-derived dendritic cells were also significantly reduced compared with control-transplanted mice. These data suggest that EBF can restrict lymphopoiesis to the B cell lineage by blocking development of other lymphoid-derived cell pathways.
引用
收藏
页码:4759 / 4769
页数:11
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