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

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CURRENT OPINION IN IMMUNOLOGY
卷 22, 期 2, 页码 177-184

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CURRENT BIOLOGY LTD
DOI: 10.1016/j.coi.2010.02.003

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  1. NIH [T32 AI07405, R01 AI54661, P01 AI22295, R21 AI075177]

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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.

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