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正常细胞和白血病细胞中分化的诱导与抑制

The induction and inhibition of differentiation in normal and leukaemic cells.

作者信息

Metcalf D

机构信息

Walter and Eliza Hall Institute of Medical Research, P.O. Royal Melbourne Hospital, Victoria, Australia.

出版信息

Philos Trans R Soc Lond B Biol Sci. 1990 Mar 12;327(1239):99-109. doi: 10.1098/rstb.1990.0046.

Abstract

For granulocytic-macrophage progenitor populations and their progeny, five glycoproteins have been identified: GM-CSF, G-CSF, multi-CSF, M-CSF and IL-6 that can regulate their proliferative activity, maturation and functional activities. The same glycoproteins also have a capacity to induce irreversible differentiation commitment in normal bipotential granulocyte-macrophage progenitors and in some myeloid leukaemic cell lines, which suggests that common cellular processes exist in both situations. The leukaemia inhibitory factor (LIF) is a glycoprotein, with intriguing properties, which can either induce differentiation in some myeloid leukaemic cell lines or prevent differentiation in normal totipotential embryonic stem cells. The data from the LIF studies suggest a genetic mechanism controlling self-generation that is relatively simple and may be common to all cells. However, the actual cellular response observed appears to depend on the nature of the responding cell.

摘要

对于粒细胞-巨噬细胞祖细胞群体及其后代,已鉴定出五种糖蛋白:粒细胞-巨噬细胞集落刺激因子(GM-CSF)、粒细胞集落刺激因子(G-CSF)、多能集落刺激因子、巨噬细胞集落刺激因子(M-CSF)和白细胞介素-6,它们可调节其增殖活性、成熟和功能活性。同样的糖蛋白也有能力在正常双潜能粒细胞-巨噬细胞祖细胞和一些髓系白血病细胞系中诱导不可逆的分化定向,这表明两种情况下存在共同的细胞过程。白血病抑制因子(LIF)是一种具有有趣特性的糖蛋白,它既可以在一些髓系白血病细胞系中诱导分化,也可以阻止正常全能胚胎干细胞的分化。来自LIF研究的数据表明,控制自我生成的遗传机制相对简单,可能对所有细胞都很常见。然而,观察到的实际细胞反应似乎取决于反应细胞的性质。

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