Zhang Zheng, Cotta Claudiu V, Stephan Robert P, deGuzman Cristina G, Klug Christopher A
Department of Microbiology, Division of Developmental and Clinical Immunology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
EMBO J. 2003 Sep 15;22(18):4759-69. doi: 10.1093/emboj/cdg464.
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.
早期B细胞因子(EBF)缺陷的小鼠在免疫球蛋白基因重排之前的祖B细胞阶段就被阻断。B细胞发育中依赖EBF的阻断发生在B细胞系定向开始时,这增加了EBF可能具有指导性作用,从未定向的多能祖细胞中指定B细胞命运的可能性。为了验证这一假设,我们用一种共表达EBF和绿色荧光蛋白(GFP)的逆转录病毒载体转导富集的造血祖细胞。用表达EBF的细胞重建的小鼠显示几乎完全没有T淋巴细胞。脾脏和外周血样本中分别有>95%和90%的GFP+EBF+成熟B细胞。与对照移植小鼠相比,自然杀伤细胞(NK)和淋巴来源的树突状细胞也显著减少。这些数据表明,EBF可以通过阻断其他淋巴来源细胞途径的发育,将淋巴细胞生成限制在B细胞系。