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Uniform neural tissue models produced on synthetic hydrogels using standard culture techniques

机译:使用标准培养技术在合成水凝胶上产生的均匀神经组织模型

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The aim of the present study was to test sample reproducibility for model neural tissues formed on synthetic hydrogels. Human embryonic stem (ES) cell-derived precursor cells were cultured on synthetic poly(ethylene glycol) (PEG) hydrogels to promote differentiation and self-organization into model neural tissue constructs. Neural progenitor, vascular, and microglial precursor cells were combined on PEG hydrogels to mimic developmental timing, which produced multicomponent neural constructs with 3D neuronal and glial organization, organized vascular networks, and microglia with ramified morphologies. Spearman’s rank correlation analysis of global gene expression profiles and a comparison of coefficient of variation for expressed genes demonstrated that replicate neural constructs were highly uniform to at least day 21 for samples from independent experiments. We also demonstrate that model neural tissues formed on PEG hydrogels using a simplified neural differentiation protocol correlated more strongly to in?vivo brain development than samples cultured on tissue culture polystyrene surfaces alone. These results provide a proof-of-concept demonstration that 3D cellular models that mimic aspects of human brain development can be produced from human pluripotent stem cells with high sample uniformity between experiments by using standard culture techniques, cryopreserved cell stocks, and a synthetic extracellular matrix. Impact statement Pluripotent stem (PS) cells have been characterized by an inherent ability to self-organize into 3D “organoids” resembling stomach, intestine, liver, kidney, and brain tissues, offering a potentially powerful tool for modeling human development and disease. However, organoid formation must be quantitatively reproducible for applications such as drug and toxicity screening. Here, we report a strategy to produce uniform neural tissue constructs with reproducible global gene expression profiles for replicate samples from multiple experiments. ]]>
机译:本研究的目的是测试在合成水凝胶上形成的模型神经组织的样品再现性。人胚胎茎(ES)细胞衍生的前体细胞在合成聚(乙二醇)(PEG)水凝胶上培养,以促进分化和自组织成模型神经组织构建体。在PEG水凝胶上组合神经祖,血管和小胶质化前体细胞以模拟发育正时,其产生3D神经元和神经胶质组织,有组织的血管网络和具有分枝形态的小胶质细胞的多组分神经构建体。 Spearman的全局基因表达谱的等级相关性分析和表达基因的变异系数的比较证明,复制神经构建体对来自独立实验的样品的至少一天21非常均匀。我们还证明使用简化的神经分化方案在PEG水凝胶上形成的模型神经组织与单独的组织培养聚苯乙烯表面上培养的样品更强烈地相关。这些结果提供了一种概念证明,其3D细胞模型可以通过使用标准培养技术,冷冻保存的细胞屑和合成细胞外基质,从人类脑发育的模拟方面的3D细胞模型从人类脑发育的模仿方面具有高样本均匀性。 。影响性多能干(PS)细胞的特征是,其特征在于一种自组织成胃,肠,肝,肾病和脑组织的三维“有机体”的固有能力,为造型的人类发展和疾病提供了一种潜在的强大工具。然而,对于药物和毒性筛选等应用,必须定量可重复细胞体形成。在此,我们报告了一种策略,以产生均匀的神经组织构建体,其可再现全球基因表达谱来复制来自多个实验的样本。 ]]>

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