Clark M R, Cooper A B, Wang L D, Aifantis I
Section of Rheumatology, University of Chicago, IL 60637, USA.
Curr Top Microbiol Immunol. 2005;290:87-103. doi: 10.1007/3-540-26363-2_5.
B cell development is a process tightly regulated by the orchestrated signaling of cytokine receptors, the pre-B cell receptor (BCR) and the B cell receptor (BCR). It commences with common lymphoid progenitors (CLP) up-regulating the expression of B cell-related genes and committing to the B cell lineage. Cytokine signaling (IL-7, stem cell factor, FLT3-L) is essential at this stage of development as it suppresses cell death, sustains proliferation and facilitates heavy chain rearrangements. As a result of heavy chain recombination, the pre-BCR is expressed, which then becomes the primary determiner of survival, cell cycle entry and allelic exclusion. In this review, we discuss the mechanisms of B cell lineage commitment and describe the signaling pathways that are initiated by the pre-BCR. Finally, we compare pre-BCR and pre-TCR structure, signal transduction and function, drawing parallels between early pre-B and pre-T cell development.
B细胞发育是一个由细胞因子受体、前B细胞受体(pre-BCR)和B细胞受体(BCR)的协同信号严格调控的过程。它始于共同淋巴祖细胞(CLP)上调B细胞相关基因的表达并确定为B细胞谱系。细胞因子信号(IL-7、干细胞因子、FLT3-L)在发育的这个阶段至关重要,因为它抑制细胞死亡、维持增殖并促进重链重排。重链重组的结果是pre-BCR表达,然后它成为存活、细胞周期进入和等位基因排斥的主要决定因素。在这篇综述中,我们讨论B细胞谱系确定的机制,并描述由pre-BCR启动的信号通路。最后,我们比较pre-BCR和pre-TCR的结构、信号转导和功能,描绘早期前B细胞和前T细胞发育之间的相似之处。