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原癌基因c-myb在正常人类造血细胞中的表达。

Expression of protooncogene c-myb in normal human hematopoietic cells.

作者信息

Kastan M B, Slamon D J, Civin C I

机构信息

Johns Hopkins Oncology Center, Baltimore, MD 21205.

出版信息

Blood. 1989 May 1;73(6):1444-51.

PMID:2469491
Abstract

Expression of the protooncogene, c-myb, in various subpopulations of normal human hematopoietic cells was characterized. Cells expressing the immature cell surface marker, CD34 (My10), were isolated by immune adherence with the "panning" technique or immunomagnetic microspheres and were shown to be strongly positive for c-myb protein expression in an immunoperoxidase assay. The CD34+ progenitor cell population was further separated into myeloid plus erythroid progenitors (CD34+, CD10-) v B-lymphoid precursors (coexpressing CD34 and CD10) by two-color FACS. Both CD34+ progenitor cell subsets strongly expressed c-myb protein by the immunoperoxidase assay. A flow cytometric assay was then developed which permitted simultaneous detection of a cell-surface antigen (to characterize lineage and stage of maturation) and the nuclear oncoprotein. This assay confirmed that CD34+ cells were strongly positive for c-myb expression and also allowed quantitative comparisons of c-myb expression in selected populations of other normal hematopoietic cells. Most human bone marrow cells appear to express some level of c-myb protein, although the CD34+ progenitor cell population expresses the highest amount.

摘要

对原癌基因c-myb在正常人造血细胞不同亚群中的表达进行了表征。通过“淘选”技术或免疫磁微球进行免疫黏附,分离出表达未成熟细胞表面标志物CD34(My10)的细胞,并在免疫过氧化物酶测定中显示其c-myb蛋白表达呈强阳性。通过双色荧光激活细胞分选术(FACS)将CD34 +祖细胞群体进一步分为髓系加红系祖细胞(CD34 +,CD10 -)和B淋巴细胞前体(共表达CD34和CD10)。在免疫过氧化物酶测定中,两个CD34 +祖细胞亚群均强烈表达c-myb蛋白。然后开发了一种流式细胞术测定法,该方法可以同时检测细胞表面抗原(以表征成熟的谱系和阶段)和核癌蛋白。该测定法证实CD34 +细胞的c-myb表达呈强阳性,并且还可以对其他正常造血细胞选定群体中的c-myb表达进行定量比较。大多数人骨髓细胞似乎表达一定水平的c-myb蛋白,尽管CD34 +祖细胞群体表达量最高。

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