Karasuyama H, Nakamura T, Nagata K, Kuramochi T, Kitamura F, Kuida K
Department of Immunology, Tokyo Metropolitan Institute of Medical Science, Japan.
Immunol Cell Biol. 1997 Apr;75(2):209-16. doi: 10.1038/icb.1997.32.
The preB cell receptor is expressed for a short period after mu heavy chain is produced, that is, at the large preB cell stage in B cell development. The severe impairment of B cell differentiation observed in mice deficient for the preB cell receptor clearly demonstrated the importance of the preB cell receptor in B cell development. Analyses of bone marrow precursor B cells in normal and B cell-deficient mutant mice indicated the preB cell receptor transduced signals to drive cell cycle and to induce allelic exclusion. The proliferation of the preB cell receptor-expressing cells leads to the selective expansion of cells which have succeeded in the productive rearrangement of mu heavy chain gene. This process builds up a preB cell pool large enough to generate sufficient numbers of mature B cells. The preB cell receptor appears to induce allelic exclusion by shutting off the expression of recombinase activation gene (RAG). In order to analyse the signal transduction pathway downstream of the preB cell receptor, we have developed a new system in which cross-linking of Ig beta expressed on bone marrow proB cells mimics the signalling through the preB cell receptor to induce differentiation from proB to small preB cells.
前B细胞受体在μ重链产生后短时间内表达,即在B细胞发育的大前B细胞阶段表达。在前B细胞受体缺陷的小鼠中观察到的B细胞分化严重受损,清楚地证明了前B细胞受体在B细胞发育中的重要性。对正常和B细胞缺陷突变小鼠骨髓前体B细胞的分析表明,前B细胞受体转导信号以驱动细胞周期并诱导等位基因排斥。表达前B细胞受体的细胞增殖导致成功进行μ重链基因有效重排的细胞选择性扩增。这一过程建立了一个足够大的前B细胞库,以产生足够数量的成熟B细胞。前B细胞受体似乎通过关闭重组酶激活基因(RAG)的表达来诱导等位基因排斥。为了分析前B细胞受体下游的信号转导途径,我们开发了一种新系统,其中骨髓前B细胞上表达的Igβ交联模拟通过前B细胞受体的信号传导,以诱导从前B细胞分化为小前B细胞。