Karasuyama H, Rolink A, Shinkai Y, Young F, Alt F W, Melchers F
Basel Institute for Immunology, Switzerland.
Cell. 1994 Apr 8;77(1):133-43. doi: 10.1016/0092-8674(94)90241-0.
Precursor B (pre-B) cells in bone marrow of normal and B cell-deficient mutant mice were analyzed for the expression of Vpre-B/lambda 5 surrogate light chain (SL). The surface expression of SL is confined to the early stages (pro-B and pre-B-I) of pre-B cell development and becomes undetectable once mu heavy chain (microH) is produced. The cell-cycle analysis revealed that cytoplasmic microH+ large cells (large pre-B-II), approximately 30% of which coexpressed SL in the cytoplasm, were most actively cycling, whereas cytoplasmic microH+ small cells (small pre-B-II) were SL- and not in cycle. The analysis of pre-B cells in B cell-deficient mice suggests that the large pre-B-II stage is a critical step for the selection and amplification of cells carrying functionally rearranged microH genes.
对正常小鼠和B细胞缺陷突变小鼠骨髓中的前体B(pre-B)细胞进行了Vpre-B/λ5替代轻链(SL)表达分析。SL的表面表达局限于pre-B细胞发育的早期阶段(前B细胞和pre-B-I),一旦产生μ重链(μH),SL就无法检测到。细胞周期分析显示,细胞质μH+大细胞(大pre-B-II)最活跃地进行细胞周期循环,其中约30%在细胞质中共表达SL,而细胞质μH+小细胞(小pre-B-II)不表达SL且不处于细胞周期。对B细胞缺陷小鼠中pre-B细胞的分析表明,大pre-B-II阶段是选择和扩增携带功能重排μH基因的细胞的关键步骤。