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首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Human cord blood-derived neural stem cell line--possible implementation in studying neurotoxicity.
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Human cord blood-derived neural stem cell line--possible implementation in studying neurotoxicity.

机译:人脐带血来源的神经干细胞系-在研究神经毒性中可能的实现。

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摘要

Neural stem cell line developed from human umbilical cord blood (HUCB-NSC) [Buzanska et al., 2003. Journal of Neurochemistry 85, 33] is an ethically uncontroversial source of stem cells, able to differentiate into neuronal, astrocytic and oligodendroglial lineages. Developmental fate decisions of HUCB-NSC can be experimentally manipulated in vitro by the presence of trophic factors, mitogenes and neuromorphogenes, but can also be influenced by neurotoxins. In this report two-dimensional (2-D) and three-dimensional (3-D) HUCB-NSC cultures are introduced as useful models for testing developmental neurotoxicity. For 2-D culture models we established a standardized method for the assessment of the growth rate and cell differentiation in 96-well plates. The proliferative capacity of the HUCB-NSC was monitored by the MTT test while their ability to differentiate into neural-like cells by immunocytochemistry of beta-tubulin III and MAP-2 for neurons, GFAP and S-100beta for astrocytes and GalC for oligodendrocytes. The 3-D culture of HUCB-NSC is represented by neurospheres. Proliferation and migration of the intermediate precursors from attached neurospheres are shown to be controlled and altered by various growth factors and further modulated by the extracellular matrix component-fibronectin. Thus, neurospheres derived from the HUCB-NSC line can represent a suitable model of the activation of dormant stem cells residing in their niche, and can be used for neurotoxic studies.
机译:从人脐带血(HUCB-NSC)发育的神经干细胞系[Buzanska等,2003。神经化学杂志85,33]是干细胞在伦理学上无争议的来源,能够分化为神经元,星形胶质细胞和少突胶质细胞系。 HUCB-NSC的发育命运决定可以通过营养因子,促有丝分裂剂和神经形态发生剂的存在在体外进行实验控制,但也可能受到神经毒素的影响。在此报告中,引入了二维(2-D)和三维(3-D)HUCB-NSC培养物作为测试发育性神经毒性的有用模型。对于二维培养模型,我们建立了评估96孔板生长速率和细胞分化的标准化方法。通过MTT试验监测HUCB-NSC的增殖能力,同时通过β-微管蛋白III和MAP-2对神经元的免疫细胞化学,GFAP和S-100beta对星形胶质细胞的免疫细胞化学以及GalC对少突胶质细胞的分化,分化为神经样细胞。 HUCB-NSC的3-D培养物由神经球代表。中间前体从附着的神经球的增殖和迁移显示受各种生长因子控制和改变,并由细胞外基质成分纤连蛋白进一步调节。因此,源自HUCB-NSC系的神经球可以代表驻留在其适当位置的休眠干细胞活化的合适模型,并且可以用于神经毒性研究。

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