共 56 条
From hematopoietic progenitors to B cells: mechanisms of lineage restriction and commitment
被引:86
作者:

Ramirez, Julita
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机构:
Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA

Lukin, Kara
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机构:
Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA

Hagman, James
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机构:
Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA
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.
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页码:177 / 184
页数:8
相关论文
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