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人类白血病T细胞系的表型分析:酶标志物、表面抗原和细胞遗传学

Phenotyping human leukemic T-cell lines: enzyme markers, surface antigens, and cytogenetics.

作者信息

Martin P J, Giblett E R, Hansen J A

出版信息

Immunogenetics. 1982;15(4):385-98. doi: 10.1007/BF00364262.

Abstract

We have compared phenotypic markers for a series of established human leukemic T-cell lines collected from different laboratories. Cell lines were tested first for genetic markers using polymorphic enzymes and then for expression of T lymphoid cell surface differentiation antigens using monoclonal antibodies. Chromosomal analysis was used as an additional method for identification of selected cell lines. On the basis of enzyme markers, it was possible to assign each of the cell lines examined to one of nine different groups. With two exceptions, surface antigen phenotypes for each of 12 cell lines were clearly distinctive. Thus, some groups of cell lines indistinguishable by enzyme markers could be further subdivided by surface antigen phenotyping. However, significant quantitative variation in expression of individual antigens was observed. In addition, surface antigen expression was not uniform in different subcultures of one cell line studied in detail. These results indicate that leukemic T-cell lines cannot be used generally as simple models of surface antigen expression in normal T-cell differentiation.

摘要

我们比较了从不同实验室收集的一系列已建立的人类白血病T细胞系的表型标记。首先使用多态性酶对细胞系进行遗传标记检测,然后使用单克隆抗体检测T淋巴细胞表面分化抗原的表达。染色体分析用作鉴定所选细胞系的附加方法。基于酶标记,有可能将所检测的每个细胞系归入九个不同组中的一组。除了两个例外,12个细胞系中每个细胞系的表面抗原表型都明显不同。因此,一些通过酶标记无法区分的细胞系组可以通过表面抗原表型进一步细分。然而,观察到个别抗原表达存在显著的定量差异。此外,在所详细研究的一个细胞系的不同传代培养物中,表面抗原表达并不均匀。这些结果表明,白血病T细胞系通常不能用作正常T细胞分化中表面抗原表达的简单模型。

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