From hematopoietic progenitors to B cells: mechanisms of lineage restriction and commitment

被引:86
作者
Ramirez, Julita [1 ]
Lukin, Kara [1 ]
Hagman, James [1 ]
机构
[1] Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA
关键词
CHROMATIN REMODELING COMPLEXES; DNA-BINDING PROTEINS; TRANSCRIPTION FACTOR; E2A PROTEINS; STEM-CELLS; LONG-TERM; FATE COMMITMENT; GENE-EXPRESSION; IKAROS; EBF;
D O I
10.1016/j.coi.2010.02.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The generation of B lymphocytes from hematopoietic progenitors requires lineage-specific transcription factors that progressively direct cell fate choices. Differentiation of hematopoietic stem cells to lymphoid progenitors requires Ikaros-dependent lineage priming and graded levels of PU.1, which are controlled by Ikaros and Gfi1. E2A drives expression of EBF1, which initiates B lineage specification. EBF1, in addition to Pax5, is necessary for commitment to the B cell lineage. As a model of gene activation in early B lymphopoiesis, mb-1 genes are activated sequentially by factors (e.g. EBF1) that initiate chromatin modifications before transcription. This review highlights the requisite interplay between transcription factors and epigenetic mechanisms in the context of B cell development.
引用
收藏
页码:177 / 184
页数:8
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