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在无饲养层细胞和外源性白血病抑制因子情况下胚胎干细胞的自我更新

Self renewal of embryonic stem cells in the absence of feeder cells and exogenous leukaemia inhibitory factor.

作者信息

Berger C N, Sturm K S

机构信息

Department of Research, Kantonsspital, Basel, Switzerland.

出版信息

Growth Factors. 1997;14(2-3):145-59. doi: 10.3109/08977199709021517.

Abstract

To evaluate the role of leukaemia inhibitory factor (LIF) for maintaining pluripotent embryonic stem (ES) cells in culture, we established several exogenous LIF-independent ES cell lines by continuous passaging in culture. The newly established ES cells, Kli and CBli, sustained their growth and remained undifferentiated in LIF-deficient medium. Analysis of chimaeric animals, produced with the beta-galactosidase transgenic Kli ES cells, revealed that LIF-independent ES cells can contribute to all embryonic germ layers. There was no detectable LIF protein in ES cell conditioned medium, and no upregulation of LIF mRNA was found. The addition of neutralising anti-LIF antibodies was not sufficient to abrogate the self renewal of the Kli ES cells. These studies suggest that the signalling pathway involving diffusible LIF can be bypassed for maintaining the pluripotency in culture, and indicate a considerable heterogeneity in growth factor dependence and differentiation of different ES cells.

摘要

为了评估白血病抑制因子(LIF)在培养中维持多能胚胎干细胞(ES细胞)的作用,我们通过在培养中连续传代建立了几种不依赖外源性LIF的ES细胞系。新建立的ES细胞系Kli和CBli在缺乏LIF的培养基中持续生长且保持未分化状态。对用β-半乳糖苷酶转基因Kli ES细胞产生的嵌合体动物进行分析发现,不依赖LIF的ES细胞可分化为所有胚胎胚层。在ES细胞条件培养基中未检测到LIF蛋白,也未发现LIF mRNA上调。添加中和性抗LIF抗体不足以消除Kli ES细胞的自我更新。这些研究表明,在培养中维持多能性时,涉及可扩散LIF的信号通路可以被绕过,并且表明不同ES细胞在生长因子依赖性和分化方面存在相当大的异质性。

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