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Neural differentiation of pluripotent cells in 3D alginate-based cultures

机译:基于3D海藻酸盐的培养物中多能细胞的神经分化

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摘要

Biomaterial-supported culture methods, allowing for directed three-dimensional differentiation of stem cells are an alternative to canonical two-dimensional cell cultures. In this paper, we evaluate the suitability of alginate for three-dimensional cultures to enhance differentiation of mouse embryonic stem cells (mESCs) towards neural lineages. We tested whether encapsulation of mESCs within alginate beads could support and/or enhance neural differentiation with respect to two-dimensional cultures. We encapsulated cells in beads of alginate with or without modification by fibronectin (Fn) or hyaluronic acid (HA). Gene expression analysis showed that cells grown in alginate and alginate-HA present increased differentiation toward neural lineages with respect to the two-dimensional control and to Fn group. Immunocytochemistry analyses confirmed these results, further showing terminal differentiation of neurons as seen by the expression of synaptic markers and markers of different neuronal subtypes. Our data show that alginate, alone or modified, is a suitable biomaterial to promote invitro differentiation of pluripotent cells toward neural fates.
机译:生物材料支持的培养方法,允许干细胞的定向三维分化,是规范的二维细胞培养的替代方法。在本文中,我们评估了藻酸盐在三维培养物中增强小鼠胚胎干细胞(mESCs)向神经谱系分化的适用性。我们测试了藻酸盐珠粒中mESC的封装是否可以支持和/或增强相对于二维培养的神经分化。我们将细胞包裹在藻酸微珠中,经过或未经过纤连蛋白(Fn)或透明质酸(HA)修饰。基因表达分析表明,相对于二维对照和Fn组,在藻酸盐和藻酸盐-HA中生长的细胞向神经谱系的分化增加。免疫细胞化学分析证实了这些结果,进一步显示了神经元的终末分化,如突触标志物和不同神经元亚型标志物的表达所见。我们的数据表明,藻酸盐单独或经修饰是促进多能细胞向神经命运体外分化的合适生物材料。

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