Hardy R R, Kemp J D, Hayakawa K
Curr Top Microbiol Immunol. 1989;152:19-25. doi: 10.1007/978-3-642-74974-2_3.
We have used 3 color FACS analysis (together with dead cell exclusion by propidium iodide) to ascertain the levels of lymphoid lineage cells present in typical young adult (2-5 month) SCID mice. Both mature and early B and T lineage cells are severely decreased (greater than 100X) in thymus, spleen and peritoneum of such mice. Analysis revealed a significant fraction of B220+ cells in bone marrow and, curiously, all such cells co-expressed a determinant recognized by the S7 antibody, likely lost early in B lineage differentiation. Thus, together with B220, expression of S7 may serve to mark the stage at which the SCID defect first becomes manifest, at least in the B lineage. This suggests that B220+/S7+ cells in bone marrow may be pro-B cells or even a lymphoid progenitor population.
我们使用三色荧光激活细胞分选分析(结合碘化丙啶排除死细胞)来确定典型的年轻成年(2 - 5个月)重症联合免疫缺陷(SCID)小鼠中存在的淋巴谱系细胞水平。在此类小鼠的胸腺、脾脏和腹膜中,成熟及早期的B和T谱系细胞均严重减少(超过100倍)。分析显示骨髓中有相当一部分B220 +细胞,奇怪的是,所有这些细胞都共同表达一种被S7抗体识别的决定簇,这可能在B谱系分化早期就已丢失。因此,与B220一起,S7的表达可能用于标记SCID缺陷首次显现的阶段,至少在B谱系中是这样。这表明骨髓中的B220 + / S7 +细胞可能是前B细胞,甚至是淋巴祖细胞群体。