Buzańska L, Habich A, Jurga M, Sypecka J, Domańska-Janik K
NeuroRepair Department, Medical Research Center, Polish Academy of Sciences, Pawińskiego 5 Str, 02-106 Warsaw, Poland.
Toxicol In Vitro. 2005 Oct;19(7):991-9. doi: 10.1016/j.tiv.2005.06.036. Epub 2005 Aug 9.
Neural stem cell line developed from human umbilical cord blood (HUCB-NSC) [Buzańska 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.
源自人脐带血的神经干细胞系(HUCB - NSC)[布赞斯卡等人,2003年。《神经化学杂志》85卷,33页]是一种在伦理上没有争议的干细胞来源,能够分化为神经元、星形胶质细胞和少突胶质细胞谱系。HUCB - NSC的发育命运决定在体外可通过营养因子、促细胞分裂剂和神经形态发生因子的存在进行实验操控,但也会受到神经毒素的影响。在本报告中,二维(2 - D)和三维(3 - D)HUCB - NSC培养被引入作为测试发育性神经毒性的有用模型。对于二维培养模型,我们建立了一种在96孔板中评估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,同时通过对神经元的β - 微管蛋白III和MAP - 2、星形胶质细胞的GFAP和S - 100β以及少突胶质细胞的半乳糖脑苷脂进行免疫细胞化学来检测其分化为神经样细胞的能力。HUCB - NSC的三维培养以神经球为代表。附着神经球的中间前体细胞的增殖和迁移显示受多种生长因子控制和改变,并进一步由细胞外基质成分纤连蛋白调节。因此,源自HUCB - NSC系的神经球可代表激活其微环境中休眠干细胞的合适模型,并可用于神经毒性研究。