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BP-1/6C3表达定义了转化前B细胞的一个分化阶段,且与恶性潜能无关。

BP-1/6C3 expression defines a differentiation stage of transformed pre-B cells and is not related to malignant potential.

作者信息

Ramakrishnan L, Wu Q, Yue A, Cooper M D, Rosenberg N

机构信息

Immunology Graduate Program, Tufts University School of Medicine, Boston, Massachusetts 02111.

出版信息

J Immunol. 1990 Sep 1;145(5):1603-8.

PMID:1974567
Abstract

BP-1 antibody recognizes a cell surface molecule related to the zinc-dependent metallopeptidases that is expressed during a narrow window early in B cell differentiation. Expression of the same molecule, as originally recognized by the mAb 6C3, is widely accepted to be associated with the complete malignant transformation of pre-B lymphoid cells. We have examined BP-1/6C3 expression in a panel of established Abelson virus-transformed cells that includes both cells analogous to pre-B cells and to less differentiated B lineage cells that have not yet completed Ig H chain gene rearrangement. This analysis reveals that many of the less differentiated transformants do not express BP-1/6C3 for an extended culture period. In contrast, virtually all transformants that are analogous to normal pre-B cells express the determinant early in their culture history. The BP-1/6C3 negative transformants are fully tumorigenic in syngeneic mice, demonstrating that BP-1/6C3 expression is not required for complete malignant transformation. Our data thus suggest that the pattern of BP-1/6C3 expression in Abelson virus-transformed cells mimics that observed in normal cells and is indicative of a differentiation event unrelated to the malignant potential of the cells.

摘要

BP-1抗体识别一种与锌依赖性金属肽酶相关的细胞表面分子,该分子在B细胞分化早期的一个狭窄时间段内表达。最初由单克隆抗体6C3识别的同一分子的表达,被广泛认为与前B淋巴细胞的完全恶性转化有关。我们检测了一组已建立的阿贝尔森病毒转化细胞中的BP-1/6C3表达,这些细胞包括类似于前B细胞的细胞以及尚未完成Ig H链基因重排的分化程度较低的B谱系细胞。该分析表明,许多分化程度较低的转化细胞在延长的培养期内不表达BP-1/6C3。相反,几乎所有类似于正常前B细胞的转化细胞在其培养历史早期都表达该决定簇。BP-1/6C3阴性转化细胞在同基因小鼠中具有完全致瘤性,表明完全恶性转化不需要BP-1/6C3表达。因此,我们的数据表明,阿贝尔森病毒转化细胞中BP-1/6C3的表达模式与正常细胞中观察到的模式相似,并且表明这是一个与细胞恶性潜能无关的分化事件。

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