Deenen G J, Van Balen I, Opstelten D
Department of Histology and Cell Biology, University of Groningen, The Netherlands.
Eur J Immunol. 1990 Mar;20(3):557-64. doi: 10.1002/eji.1830200315.
The cycling B precursor cells in rat bone marrow (BM) that carry the B220 antigen and no surface Ig daily produce 780 million new cells. The pool of recirculating B lymphocytes in the rat, however, renew at a rate of only about 40 million cells/day. To analyze at which stages in B lymphocyte genesis the cell loss occurs, we identified post-mitotic cells in the rat BM B lineage, and determined their renewal rates. We used 5-bromo-deoxyuridine (BrdUrd) to label DNA-synthesizing cells, identifying incorporated BrdUrd with the mouse monoclonal antibody BU-1. B lineage cell subsets were identified by the markers HIS24 antigen (rat B220), terminal deoxynucleotidyl transferase (TdT), Ig mu heavy chain, and complete Ig. By use of double and triple immunocytology, we determined the extent of BrdUrd incorporation in the various B lineage compartments [HIS24+TdT-Ig-, TdT+, cytoplasmic mu chain (c mu)+ surface (s) IgM- pre-B, sIgM+ B]. Both sIgM+ B lymphocytes and all B precursors with cell diameters less than 11-12 microns were virtually devoid of DNA synthesis, as indicated by S-phase indices below 2%. In contrast, S-phase indices of large B precursors ranged between 43%-66%. We established the renewal rates of nondividing BM B lineage cells by placing osmotic minipumps containing BrdUrd subcutaneously in the flank of rats. The nondividing BM B lineage cells all renewed rapidly at rates between 2.4% and 5.6%/h, representing average half-lives of 29 to 12 h. In absolute numbers, the renewal/day/whole body BM was 165 X 10(6) for sIgM+ B lymphocytes, 422 X 10(6) for small c mu+ sIgM- pre-B cells, 89 X 10(6) for small TdT+ cells and 35 X 10(6) for small HIS24+TdT-Ig- cells. Assuming that recirculating B lymphocytes in the periphery are the descendants of BM sIgM+ B lymphocytes, which in their turn are the progeny of small pre-B cells, the renewal data indicate the following. Of the 165 million potentially available BM B lymphocytes, only 40 million cells become incorporated in the pool of recirculating B lymphocytes, representing a loss of 75%. BM B lymphocytes, in turn, use only (165/422 X 100% = ) 40% of the potential output from their immediate precursors. The 60% loss that occurs here may reflect the extent of aberrant Ig light chain gene rearrangement in normal B lymphocyte genesis.(ABSTRACT TRUNCATED AT 400 WORDS)
大鼠骨髓(BM)中携带B220抗原且无表面免疫球蛋白(Ig)的循环B前体细胞每天产生7.8亿个新细胞。然而,大鼠体内循环B淋巴细胞库的更新速率仅约为每天4000万个细胞。为了分析B淋巴细胞生成过程中细胞损失发生在哪些阶段,我们鉴定了大鼠BM B系中的有丝分裂后细胞,并确定了它们的更新速率。我们使用5-溴脱氧尿苷(BrdUrd)标记DNA合成细胞,用小鼠单克隆抗体BU-1识别掺入的BrdUrd。通过HIS24抗原(大鼠B220)、末端脱氧核苷酸转移酶(TdT)、Igμ重链和完整Ig等标志物鉴定B系细胞亚群。通过双重和三重免疫细胞化学方法,我们确定了不同B系区室[HIS24 + TdT - Ig -、TdT +、胞质μ链(cμ)+表面(s)IgM -前B细胞、sIgM + B细胞]中BrdUrd的掺入程度。sIgM + B淋巴细胞和所有细胞直径小于11 - 12微米的B前体细胞几乎没有DNA合成,S期指数低于2%表明了这一点。相比之下,大型B前体细胞的S期指数在43% - 66%之间。我们通过将含有BrdUrd的渗透微型泵皮下植入大鼠侧腹来确定不分裂的BM B系细胞的更新速率。不分裂的BM B系细胞均以2.4%至5.6%/小时的速率快速更新,平均半衰期为29至12小时。以绝对数量计,全身BM中sIgM + B淋巴细胞的每日更新量为1.65×10⁶,小cμ + sIgM -前B细胞为4.22×10⁶,小TdT +细胞为8.9×10⁶,小HIS24 + TdT - Ig -细胞为3.5×10⁶。假设外周循环B淋巴细胞是BM sIgM + B淋巴细胞的后代,而BM sIgM + B淋巴细胞又是小前B细胞的后代,更新数据表明如下情况。在1.65亿个潜在可用的BM B淋巴细胞中,只有4000万个细胞进入循环B淋巴细胞库,损失率为75%。反过来,BM B淋巴细胞仅利用其直接前体细胞潜在产量的(165/422×100% =)40%。此处发生的60%的损失可能反映了正常B淋巴细胞生成过程中异常Ig轻链基因重排的程度。(摘要截短于400字)