Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, 565-0871, Japan,
Int J Hematol. 2013 Oct;98(4):382-9. doi: 10.1007/s12185-013-1424-7. Epub 2013 Sep 3.
Although B lymphopoiesis is one of the best-defined paradigms in cell differentiation, our knowledge of the regulatory mechanisms underlying its earliest processes, in which hematopoietic stem cells (HSCs) enter the B lineage, is limited. However, recent methodological advances in sorting progenitor cells and monitoring their epigenetic features have increased our understanding of HSC activities. It is now known that even the highly enriched HSC fraction is heterogeneous in terms of lymphopoietic potential. While surface markers and reporter proteins provide information on the sequential differentiation of B-lineage progenitors, complex interactions between transcription factors have also been shown to play a major role in this process. Epigenetic regulation of histones, nucleosomes, and chromatin appears to play a crucial background role in this elaborate transcription network. In this review, we summarize recent findings on the physiological processes of early B-lineage differentiation, which provides a new paradigm for understanding the harmonious action of genetic and epigenetic mechanisms.
尽管 B 细胞发生是细胞分化中最明确的范例之一,但我们对造血干细胞 (HSCs) 进入 B 谱系的最早过程的调控机制的了解是有限的。然而,最近在分选祖细胞和监测其表观遗传特征方面的方法学进展增加了我们对 HSC 活性的理解。现在已知,即使是高度富集的 HSC 部分,在淋巴发生潜力方面也是异质的。虽然表面标记物和报告蛋白提供了关于 B 谱系祖细胞的顺序分化的信息,但转录因子之间的复杂相互作用也被证明在这个过程中起着主要作用。组蛋白、核小体和染色质的表观遗传调控似乎在这个复杂的转录网络中起着至关重要的背景作用。在这篇综述中,我们总结了关于早期 B 细胞分化的生理过程的最新发现,为理解遗传和表观遗传机制的协调作用提供了一个新的范例。