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人骨髓的流式细胞术分析。IV. 正常造血过程中T-200共同白细胞抗原的差异定量表达。

Flow cytometric analysis of human bone marrow. IV. Differential quantitative expression of T-200 common leukocyte antigen during normal hemopoiesis.

作者信息

Shah V O, Civin C I, Loken M R

机构信息

Becton Dickinson Monoclonal Center, Mountain View, CA 94039.

出版信息

J Immunol. 1988 Mar 15;140(6):1861-7.

PMID:2964486
Abstract

We have correlated the intensity of expression of CD45 Ag (T200 common leukocyte Ag) with mAb reactive with various lineages of hemopoietic cells in normal human bone marrow by using two-color immunofluorescence on a flow cytometer. Mature T lymphocytes (CD3+) and NK cells (CD16+ or CD11b+) expressed CD45 at the highest intensity. B lymphoid cells (CD19+) had three distinct levels of CD45 Ag expression. The bright CD45(3+) cells were mature B cells (CD19+, CD20+), whereas the less intense CD45(2+) cells were less mature B lymphoid cells (CD19+, CD10+). The dim CD45+ cells were very early, B lymphoid precursor cells (CD19+, CD10(2+), CD34+). The intensity of CD45 expression increased as cells matured in the monocytic lineage (CD14+, CD11b+). Among marrow granulocytic cells, CD45 intensity did not change on cells during maturation. Within the erythroid lineage, the most immature cells were CD45+ dim, and CD45 expression decreased during erythroid maturation to become undetectable on mature E. Hemopoietic progenitor cells (CD34+) expressed low levels of CD45 Ag. Expression of CD45R on marrow cells also showed intensity differences on different lineages. All NK cells (CD16+) were positive for CD45R, whereas only about one-half of the T lymphocytes (CD3+) were positive for CD45R. Almost all the cells in the erythroid and myelomonocytic lineages were CD45R-. Quantitative differences in expression of CD45R were observed on marrow B lymphoid cells which were correlated with the expression of CD45. The results show that quantitative changes in CD45 Ag expression accompany the differentiation and maturation of cells in the bone marrow. Comparisons with CD45R showed that this Ag was not always correlated with CD45. Since these Ag are the products of the same gene, these data indicate that the regulation of expression of the T200 molecules during normal hemopoietic development must be both quantitative and qualitative.

摘要

我们通过在流式细胞仪上进行双色免疫荧光分析,将正常人骨髓中CD45抗原(T200共同白细胞抗原)的表达强度与与造血细胞不同谱系反应的单克隆抗体相关联。成熟T淋巴细胞(CD3 +)和NK细胞(CD16 +或CD11b +)表达CD45的强度最高。B淋巴细胞(CD19 +)具有三种不同水平的CD45抗原表达。明亮的CD45(3+)细胞是成熟B细胞(CD19 +,CD20 +),而强度较低的CD45(2+)细胞是不太成熟的B淋巴细胞(CD19 +,CD10 +)。暗淡的CD45 +细胞是非常早期的B淋巴细胞前体细胞(CD19 +,CD10(2+),CD34 +)。随着细胞在单核细胞谱系(CD14 +,CD11b +)中成熟,CD45表达强度增加。在骨髓粒细胞中,细胞成熟过程中CD45强度没有变化。在红细胞谱系中,最不成熟的细胞是CD45 +暗淡的,并且在红细胞成熟过程中CD45表达降低,在成熟红细胞上变得无法检测到。造血祖细胞(CD34 +)表达低水平的CD45抗原。骨髓细胞上CD45R的表达在不同谱系上也显示出强度差异。所有NK细胞(CD16 +)CD45R呈阳性,而只有约一半的T淋巴细胞(CD3 +)CD45R呈阳性。红细胞和骨髓单核细胞谱系中的几乎所有细胞都是CD45R -。在骨髓B淋巴细胞上观察到CD45R表达的定量差异,这与CD45的表达相关。结果表明,CD45抗原表达的定量变化伴随着骨髓中细胞的分化和成熟。与CD45R的比较表明,该抗原并不总是与CD45相关。由于这些抗原是同一基因的产物,这些数据表明在正常造血发育过程中T200分子表达的调节必须是定量的和定性的。

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