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造血干细胞白血病中的免疫球蛋白基因组织与表达

Immunoglobulin gene organisation and expression in haemopoietic stem cell leukaemia.

作者信息

Ford A M, Molgaard H V, Greaves M F, Gould H J

出版信息

EMBO J. 1983;2(6):997-1001. doi: 10.1002/j.1460-2075.1983.tb01533.x.

Abstract

We have analysed the organisation and expression of mu genes in the granulocytic phase and in the lymphoid and myeloid blast crises of Philadelphia chromosome (Ph1) chronic granulocytic leukaemia (CGL), a leukaemia which is known to arise in multipotential stem cells. We find that mu chain gene rearrangement occurs exclusively in lymphoid blast crisis leading in some, but not all, cases to the synthesis of small amounts of cytoplasmic mu chains characteristic of early pre-B lymphocytes. In Southern blots, only one or two rearranged mu chain genes are seen, suggesting that a clonal event leading to blast crisis can occur in a committed B cell precursor rather than in the multipotential stem cell precursor, in which the Ph1 chromosome originated. The pattern of mu gene rearrangement observed in Ph1 CGL blast crisis is compared with that in normal B cells, other B lineage malignancies, myeloid leukaemias and T cell leukaemias.

摘要

我们分析了费城染色体(Ph1)慢性粒细胞白血病(CGL)粒细胞期、淋巴母细胞危象期及髓母细胞危象期μ基因的组织和表达情况,已知这种白血病起源于多能干细胞。我们发现μ链基因重排仅发生在淋巴母细胞危象期,在一些(但并非全部)病例中导致少量早期前B淋巴细胞特征性的胞质μ链合成。在Southern印迹中,仅可见一两个重排的μ链基因,这表明导致母细胞危象的克隆事件可能发生在定向B细胞前体而非Ph1染色体起源的多能干细胞前体中。将Ph1 CGL母细胞危象期观察到的μ基因重排模式与正常B细胞、其他B系恶性肿瘤、髓系白血病及T细胞白血病中的模式进行了比较。

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