Magnetic separation of undifferentiated mouse Embryonic Stem (ES) cells from neural progenitor cultures using a microfluidic device

A. F. Sousa, J. Loureiro, M. M. Diogo, J. Cabral, P. Freitas
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Abstract

Embryonic Stem (ES) cells are cell lines derived directly from the pre-implantation embryo. The generation of pure populations of neural progenitors from ES cells and their further differentiation into neurons, astrocytes and oligodendrocytes allows the potential use of these cells for the cure of neurodegenerative diseases and for neural drugs testing. An integrated device based on magnetophoresis, including microfluidic channels and incorporated high magnetic field gradients, was used to control the motion of cells, labeled with magnetic particles (MPs), through a biochip. In this work, the magnetophoretic device has been used for depletion of tumorogenic pluripotent stem cells from 46C mouse ES cell cultures by the specific recognition and labeling of the stage specific embryonic antigen 1 (SSEA-1). Purity degrees ranging from 95% to 99,5% were obtained and determined by flow cytometry analysis
利用微流体装置磁分离未分化小鼠胚胎干(ES)细胞与神经祖细胞的培养
胚胎干细胞(ES)是直接从胚胎着床前获得的细胞系。从胚胎干细胞中产生的纯神经祖细胞群及其进一步分化为神经元、星形胶质细胞和少突胶质细胞,使这些细胞有可能用于神经退行性疾病的治疗和神经药物测试。基于磁泳术的集成装置,包括微流控通道和高磁场梯度,用于通过生物芯片控制磁性颗粒(MPs)标记的细胞运动。在这项工作中,磁电泳装置已被用于通过特异性识别和标记阶段特异性胚胎抗原1 (SSEA-1)来消耗46C小鼠ES细胞培养的致瘤多能干细胞。纯度范围为95% ~ 99.5%,通过流式细胞术分析确定
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