Barneda-Zahonero Bruna, Roman-Gonzalez Lidia, Collazo Olga, Mahmoudi Tokameh, Parra Maribel
Cellular Differentiation Group, Cancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), Avenida Gran Via s/n km 2.7, 08907 L'Hospitalet de Llobregat, Barcelona, Spain.
Comp Funct Genomics. 2012;2012:564381. doi: 10.1155/2012/564381. Epub 2012 Aug 26.
B cell development is a multistep process that is tightly regulated at the transcriptional level. In recent years, investigators have shed light on the transcription factor networks involved in all the differentiation steps comprising B lymphopoiesis. The interplay between transcription factors and the epigenetic machinery involved in establishing the correct genomic landscape characteristic of each cellular state is beginning to be dissected. The participation of "epigenetic regulator-transcription factor" complexes is also crucial for directing cells during reprogramming into pluripotency or lineage conversion. In this context, greater knowledge of epigenetic regulation during B cell development, transdifferentiation, and reprogramming will enable us to understand better how epigenetics can control cell lineage commitment and identity. Herein, we review the current knowledge about the epigenetic events that contribute to B cell development and reprogramming.
B细胞发育是一个多步骤过程,在转录水平上受到严格调控。近年来,研究人员已经阐明了参与B淋巴细胞生成所有分化步骤的转录因子网络。转录因子与参与建立每种细胞状态特征性正确基因组格局的表观遗传机制之间的相互作用正开始被剖析。“表观遗传调节因子-转录因子”复合物的参与对于在重编程为多能性或谱系转换过程中引导细胞也至关重要。在这种背景下,对B细胞发育、转分化和重编程过程中表观遗传调控的更多了解将使我们能够更好地理解表观遗传学如何控制细胞谱系定向和特性。在此,我们综述了有关促成B细胞发育和重编程的表观遗传事件的当前知识。