LeBien T W, Elstrom R L, Moseley M, Kersey J H, Griesinger F
Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis 55455.
Blood. 1990 Sep 15;76(6):1196-200.
Fetal bone marrow B lineage cells representing multiple stages of B cell development were isolated by two-color cell sorting and analyzed for immunoglobulin H and T-cell receptor (TCR) gamma and delta gene rearrangements. Analysis of CD10+/surface mu- cells using a JH probe revealed a high frequency of rearrangements; some of these rearrangements used the 3' D region gene DQ52. Analysis of CD10+/surface mu- cells revealed no detectable TCR-gamma or -delta rearrangements, nor were TCR-delta rearrangements detected in CD10+/surface mu+ cells, despite the limited repertoire of these genes. These observations are surprising given the high frequency of TCR delta/gamma rearrangements in B cell precursor acute lymphoblastic leukemia, and identify a potential difference in patterns of gene rearrangement that distinguish normal and leukemic B cell precursors.
通过双色细胞分选分离出代表B细胞发育多个阶段的胎儿骨髓B谱系细胞,并对免疫球蛋白H以及T细胞受体(TCR)γ和δ基因重排进行分析。使用JH探针分析CD10 + /表面μ-细胞发现重排频率很高;其中一些重排使用了3'D区域基因DQ52。对CD10 + /表面μ-细胞的分析未发现可检测到的TCR-γ或-δ重排,并且在CD10 + /表面μ+细胞中也未检测到TCR-δ重排,尽管这些基因的库有限。鉴于B细胞前体急性淋巴细胞白血病中TCRδ/γ重排的高频率,这些观察结果令人惊讶,并确定了区分正常和白血病B细胞前体的基因重排模式的潜在差异。