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正常和恶性造血过程中细胞内CD68分子表达的流式细胞术分析

Flow cytometric analysis of intracellular CD68 molecule expression in normal and malignant haemopoiesis.

作者信息

Strobl H, Scheinecker C, Csmarits B, Majdic O, Knapp W

机构信息

Institute of Immunology, Vienna International Research Cooperation Centre at SFI, University of Vienna, Austria.

出版信息

Br J Haematol. 1995 Aug;90(4):774-82. doi: 10.1111/j.1365-2141.1995.tb05195.x.

Abstract

CD68 molecules are heavily glycosylated lysosomal membrane constituents of unknown function with strong expression in monocytes and macrophages. Using flow cytometry, we quantified expression levels of CD68 molecules in normal and malignant haemopoietic cells. CD68 molecules are intensely expressed in the cytoplasm and weakly on the surface of mature CD14+ monocytes. CD68 expression seems to start very early during granulomonopoietic differentiation. Virtually all myeloperoxidase (MPO)+ bone marrow cells coexpress CD68 and similar proportions of CD34+ progenitor cells weakly express CD68 or MPO molecules. During further differentiation, CD68 expression is strongly up-regulated in early MPO+ precursor cells which lack lactoferrin (LF) and CD14 molecules. Compared to these, more mature MPO+LF+ bone marrow and peripheral blood granulocytes express considerable lower levels of CD68. In-line with this broad expression, all investigated acute myeloid leukaemia (AML) cases, classified as FAB M1-M5, were CD68 positive, and compared to normal CD34+ bone marrow cells. CD34+ AML blast cells expressed increased levels. CD68 expression is, however, not restricted to cells of myeloid origin, because a subset (40 +/- 15%, n = 6) of CD19+ peripheral blood B-lymphocytes and 50% of B-ALL are also weakly positive. In contrast, normal CD3+ lymphocytes lack (< 3%, n = 6) CD68 and only low proportions (6 +/- 3%, n = 6) of CD56+ NK cells are CD68+. Also, all investigated T-ALL cases (n = 6) lacked CD68.

摘要

CD68分子是高度糖基化的溶酶体膜成分,功能未知,在单核细胞和巨噬细胞中强烈表达。我们使用流式细胞术对正常和恶性造血细胞中CD68分子的表达水平进行了定量。CD68分子在成熟CD14+单核细胞的细胞质中强烈表达,在其表面表达较弱。CD68的表达似乎在粒细胞单核细胞分化过程中很早就开始了。几乎所有髓过氧化物酶(MPO)+骨髓细胞都共表达CD68,类似比例的CD34+祖细胞弱表达CD68或MPO分子。在进一步分化过程中,在缺乏乳铁蛋白(LF)和CD14分子的早期MPO+前体细胞中,CD68表达强烈上调。与这些细胞相比,更成熟的MPO+LF+骨髓和外周血粒细胞表达的CD68水平要低得多。与此广泛表达一致,所有被分类为FAB M1 - M5的急性髓系白血病(AML)病例均为CD68阳性,与正常CD34+骨髓细胞相比,CD34+ AML原始细胞表达水平升高。然而,CD68的表达并不局限于髓系来源的细胞,因为一部分(40±15%,n = 6)CD19+外周血B淋巴细胞和50%的B - ALL也呈弱阳性。相比之下,正常CD3+淋巴细胞缺乏(< 3%,n = 6)CD68,只有低比例(6±3%,n = 6)的CD56+ NK细胞为CD68阳性。此外,所有研究的T - ALL病例(n =

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