断点群集区域
转录因子
生物
B细胞
细胞生物学
IRF4公司
等离子体电池
记忆B细胞
细胞分化
细胞命运测定
抗体
免疫学
遗传学
基因
作者
Ryo Shinnakasu,Tomohiro Kurosaki
标识
DOI:10.1016/j.coi.2017.03.003
摘要
Memory B cell generation and antibody production result from a differentiation process that begins when the surface BCR on naïve B cells binds an antigen. How the choice between these fates is tempo-spatially regulated is still obscure, but recent advances have reinforced the concept that the combination of B cell-intrinsic heterogeneity and -extrinsic heterogeneity provided by cells such as T cells is a key determinant. As molecular regulators, the transcription factors IRF4 and Bach2, which participate in these fate choices, have been emerging.
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