Department of Cellular and Molecular Immunology, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Department of Cellular and Molecular Immunology, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Trends Genet. 2018 Apr;34(4):257-269. doi: 10.1016/j.tig.2017.12.014. Epub 2018 Jan 11.
Hematopoiesis is regulated by signals from the microenvironment, transcription factor networks, and changes of the epigenetic landscape. Transcription factors interact with and shape chromatin to allow for lineage- and cell type-specific changes in gene expression. During B lymphopoiesis, epigenetic regulation is observed in multilineage progenitors in which a specific chromatin context is established, at the onset of the B cell differentiation when early B cell factor 1 (EBF1) induces lineage-specific changes in chromatin, during V(D)J recombination and after antigen-driven activation of B cells and terminal differentiation. In this review, we discuss the epigenetic changes underlying B cell differentiation, focusing on the role of transcription factor EBF1 in B cell lineage priming.
造血是由微环境信号、转录因子网络和表观遗传景观变化调节的。转录因子相互作用并塑造染色质,以允许谱系和细胞类型特异性的基因表达变化。在 B 淋巴细胞发生过程中,多能祖细胞中观察到表观遗传调控,其中在 B 细胞分化开始时,早期 B 细胞因子 1 (EBF1) 诱导染色质的谱系特异性变化时,建立特定的染色质环境,在 V(D)J 重组和抗原驱动的 B 细胞激活以及终末分化后。在这篇综述中,我们讨论了 B 细胞分化的表观遗传变化,重点讨论了转录因子 EBF1 在 B 细胞谱系启动中的作用。