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小鼠巨噬细胞前体的特性。I. 巨噬细胞前体杂交体的产生、表型及分化

Murine macrophage precursor characterization. I. Production, phenotype and differentiation of macrophage precursor hybrids.

作者信息

Leenen P J, Slieker W A, Melis M, Van Ewijk W

机构信息

Department of Cell Biology II and Immunology, Erasmus University, Rotterdam, The Netherlands.

出版信息

Eur J Immunol. 1990 Jan;20(1):15-25. doi: 10.1002/eji.1830200104.

Abstract

This study reports on the earliest stages of mononuclear phagocyte differentiation. A crucial question in this developmental process is whether mature macrophage (M phi) heterogeneity is already appointed at the precursor cell level. For this purpose, we produced clonal populations of mononuclear phagocytes from bone marrow culture by somatic cell hybridization with two hypoxanthine, aminopterin, thymidine-sensitive myeloid cell lines. A panel of 22 stable hybrids was obtained from these fusions. Differentiation stage analysis of the hybrids indicated that all cell lines had immature mononuclear phagocyte characteristics. The hybrids exhibited typical myeloid morphology and mainly nonadherent growth. Mature M phi features, such as expression of the cell surface antigens Mac-1, Mac-2 and F4/80, phagocytosis of latex beads, and expression of nonspecific esterase and acid phosphatase activity, were virtually absent. The immature M phi markers Thy-1, MIV25 and MIV52, on the other hand, were readily expressed, although heterogeneity was observed among different hybrid cell lines. We then analyzed the differentiation potential of seven hybrids by culture of the cells in the presence of post-lipopolysaccharide serum supplemented with interferon-gamma and found that the expression of mature M phi characteristics was induced. However, the various hybrids showed divergent patterns of mature M phi marker induction. R0C2 cells, for instance, showed extensive morphological and phenotypical differentiation without concomitant induction of phagocytosis. In contrast, W1C4 cells showed significant induction of phagocytosis without simultaneous increase of phosphatase and esterase activity. R1C1 cells were unique in the strong induction of Ia antigen expression. Together, our data indicate that (a) early M phi differentiation stages can be rescued by somatic cell hybridization, and that (b) the obtained cell lines are able to mature according to divergent differentiation programs.

摘要

本研究报道了单核吞噬细胞分化的最早阶段。在这个发育过程中一个关键问题是成熟巨噬细胞(M phi)的异质性在祖细胞水平是否已经确定。为此,我们通过与两种次黄嘌呤、氨基蝶呤、胸腺嘧啶核苷敏感的髓系细胞系进行体细胞杂交,从骨髓培养物中产生了单核吞噬细胞的克隆群体。从这些融合中获得了一组22个稳定的杂交细胞系。对杂交细胞系的分化阶段分析表明,所有细胞系都具有未成熟单核吞噬细胞的特征。杂交细胞表现出典型的髓系形态,主要为非贴壁生长。成熟M phi的特征,如细胞表面抗原Mac-1、Mac-2和F4/80的表达、乳胶珠的吞噬作用以及非特异性酯酶和酸性磷酸酶活性的表达,实际上并不存在。另一方面,未成熟M phi标记物Thy-1、MIV25和MIV52很容易表达,尽管在不同的杂交细胞系之间观察到了异质性。然后,我们通过在添加了γ干扰素的脂多糖后血清存在的情况下培养细胞,分析了7个杂交细胞系的分化潜能,发现成熟M phi特征的表达被诱导。然而,不同的杂交细胞系显示出成熟M phi标记物诱导的不同模式。例如,R0C2细胞表现出广泛的形态和表型分化,但没有伴随吞噬作用的诱导。相反,W1C4细胞表现出吞噬作用的显著诱导,而磷酸酶和酯酶活性没有同时增加。R1C1细胞在Ia抗原表达的强烈诱导方面是独特的。总之,我们的数据表明:(a)早期M phi分化阶段可以通过体细胞杂交挽救,并且(b)所获得的细胞系能够根据不同的分化程序成熟。

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