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重组大鼠干细胞因子(c-kit配体)增强培养体系中小鼠胚细胞集落的形成。

Enhancement of murine blast cell colony formation in culture by recombinant rat stem cell factor, ligand for c-kit.

作者信息

Tsuji K, Zsebo K M, Ogawa M

机构信息

Department of Medicine, Medical University of South Carolina.

出版信息

Blood. 1991 Sep 1;78(5):1223-9.

PMID:1715219
Abstract

Mice with W mutations characterized by hypopigmentation, sterility, anemia, and mast cell deficiency have abnormalities in c-kit, a receptor with tyrosine kinase activity. Recently, the ligand for c-kit was cloned by investigators in several laboratories. Zsebo et al identified and cloned a gene for a cytokine termed stem cell factor (SCF) in the medium conditioned by buffalo rat liver cells, and this cytokine proved to be c-kit ligand. We have examined the effects of recombinant rat SCF (rrSCF) on colony formation from primitive hematopoietic progenitors in culture. rrSCF and erythropoietin (Ep) supported formation of granulocyte/macrophage (GM) colonies as well as a small number of multilineage and blast cell colonies from marrow cells of normal mice. We then examined the effects of rrSCF using marrow and spleen cells of mice that had been treated with 150 mg/kg 5-fluorouracil (5-FU). Unlike single factors, combinations of factors such as rrSCF plus interleukin-3 (IL-3), rrSCF plus IL-6, and rrSCF plus granulocyte colony-stimulating factor (G-CSF) markedly stimulated the growth of multilineage colonies. In contrast to these factor combinations and a combination of IL-3 and IL-6, a combination of rrSCF and IL-4 did not support multilineage colony formation. Mapping studies of the development of multipotential blast cell colonies further indicated that rrSCF, like IL-6, G-CSF, and IL-11, shortens the dormant period in which the stem cells reside. When we tested the effects of rrSCF using pooled blast cells, which are highly enriched for progenitors and are devoid of stromal cells, rrSCF plus Ep supported formation of only a few multilineage colonies, indicating that rrSCF itself is ineffective in support of the proliferation of multipotential progenitors. However, rrSCF supported formation of a significant number of neutrophil and neutrophil/macrophage colonies from pooled blast cells, indicating that rrSCF is able to support directly the proliferation of progenitors in neutrophil/monocyte lineages. c-kit ligand may play important roles in adult hematopoiesis.

摘要

具有W突变的小鼠表现为色素沉着不足、不育、贫血和肥大细胞缺乏,其c-kit(一种具有酪氨酸激酶活性的受体)存在异常。最近,几个实验室的研究人员克隆了c-kit的配体。泽博等人在水牛大鼠肝细胞条件培养基中鉴定并克隆了一种名为干细胞因子(SCF)的细胞因子基因,这种细胞因子被证明是c-kit配体。我们研究了重组大鼠SCF(rrSCF)对培养中原始造血祖细胞集落形成的影响。rrSCF和促红细胞生成素(Ep)支持正常小鼠骨髓细胞形成粒细胞/巨噬细胞(GM)集落以及少量多系和原始细胞集落。然后,我们使用经150mg/kg 5-氟尿嘧啶(5-FU)处理的小鼠的骨髓和脾细胞研究了rrSCF的作用。与单一因子不同,rrSCF加白细胞介素-3(IL-3)、rrSCF加IL-6以及rrSCF加粒细胞集落刺激因子(G-CSF)等因子组合显著刺激了多系集落的生长。与这些因子组合以及IL-3和IL-6的组合相反,rrSCF和IL-4的组合不支持多系集落形成。对多能原始细胞集落发育的定位研究进一步表明,rrSCF与IL-6、G-CSF和IL-11一样,缩短了干细胞所处的休眠期。当我们使用高度富集祖细胞且不含基质细胞的混合原始细胞测试rrSCF的作用时,rrSCF加Ep仅支持形成少数多系集落,表明rrSCF本身在支持多能祖细胞增殖方面无效。然而,rrSCF支持从混合原始细胞形成大量中性粒细胞和中性粒细胞/巨噬细胞集落,表明rrSCF能够直接支持中性粒细胞/单核细胞谱系中祖细胞的增殖。c-kit配体可能在成人造血中起重要作用。

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