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Single cell derived murine embryonic stem cell clones stably express Rex1-specific green fluorescent protein and their differentiation study

机译:单细胞来源的小鼠胚胎干细胞克隆稳定表达Rex1特异性绿色荧光蛋白及其分化研究

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摘要

Embryonic stem cells (ESCs) often display high rates of apoptosis and spontaneous differentiation in routine culture, thus bring the proliferation of these cells highly inefficient. Moreover, little is known about the factors that are indispensable for sustaining self-renewal. To surmount these issues, we established transgenic mES cell lines expressing the enhanced green fluorescent protein (EGFP) under the control of the Rex1 promoter which is a key regulator of pluripotency in ES cells. In addition, we provided a simplified and improved protocol to derive transgenic mESCs from single cell. Finally, we showed that embryoid body (EB) development was faster than adherent differentiation in terms of differentiation ratio by real-time tracking of the EGFP expression. Therefore, these cell lines can be tracked and selected both in vitro and in vivo and should be invaluable for studying the factors that are indispensable for maintaining pluripotency. (c) 2007 Elsevier Inc. All rights reserved.
机译:胚胎干细胞(ESC)在常规培养中通常显示出高凋亡率和自发分化能力,因此使这些细胞的增殖效率极低。此外,对于维持自我更新必不可少的因素知之甚少。为了克服这些问题,我们建立了在Rex1启动子的控制下表达增强的绿色荧光蛋白(EGFP)的转基因mES细胞系,该启动子是ES细胞多能性的关键调节剂。此外,我们提供了一种简化和改进的协议,可以从单细胞中获得转基因mESC。最后,我们通过实时追踪EGFP的表达,显示出类胚体(EB)的发育比粘附性分化快。因此,这些细胞系可以在体外和体内进行追踪和选择,对于研究维持多能性必不可少的因素具有重要的意义。 (c)2007 Elsevier Inc.保留所有权利。

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