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首页> 外文期刊>Scientific reports. >Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey
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Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey

机译:使用来自Cynomolgus猴的诱导多能干细胞的定向分化建立平移内皮细胞模型

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Due to their broad differentiation potential, pluripotent stem cells (PSCs) offer a promising approach for generating relevant cellular models for various applications. While human PSC-based cellular models are already advanced, similar systems for non-human primates (NHPs) are still lacking. However, as NHPs are the most appropriate animals for evaluating the safety of many novel pharmaceuticals, the availability of in vitro systems would be extremely useful to bridge the gap between cellular and animal models. Here, we present a NHP in vitro endothelial cell system using induced pluripotent stem cells (IPSCs) from Cynomolgus monkey (Macaca fascicularis). Based on an adapted protocol for human IPSCs, we directly differentiated macaque IPSCs into endothelial cells under chemically defined conditions. The resulting endothelial cells can be enriched using immuno-magnetic cell sorting and display endothelial marker expression and function. RNA sequencing revealed that the differentiation process closely resembled vasculogenesis. Moreover, we showed that endothelial cells derived from macaque and human IPSCs are highly similar with respect to gene expression patterns and key endothelial functions, such as inflammatory responses. These data demonstrate the power of IPSC differentiation technology to generate defined cell types for use as translational in vitro models to compare cell type-specific responses across species.
机译:由于它们的宽分化潜力,多能干细胞(PSC)提供了一种有希望的方法,用于为各种应用产生相关的细胞模型。虽然基于人的PSC的蜂窝模型已经前进,但仍然缺乏类似的非人类灵长类动物(NHPS)的类似系统。然而,随着NHPS是用于评估许多新型药物安全的最合适的动物,体外系统的可用性将极其有用,以弥合细胞和动物模型之间的差距。在这里,我们使用来自Cynomolgus猴(Macaca Fascularis)的诱导多能干细胞(IPSC)的NHP体外内皮细胞系统。基于适用于人IPSCS的适应方案,在化学定义的条件下,我们将猕猴IPSC直接分化为内皮细胞。可以使用免疫磁性细胞分选和显示内皮标记表达和功能来富集所得内皮细胞。 RNA测序表明,分化过程非常类似于血管发生。此外,我们表明,衍生自猕猴和人IPSCs的内皮细胞对于基因表达模式和关键内皮功能(例如炎症反应)非常相似。这些数据展示了IPSC差异化技术的力量,以产生定义的细胞类型,以用作平移体外模型,以比较跨物种的细胞类型的响应。

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