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三维微流控细胞培养中神经上皮干细胞向功能性多巴胺能神经元的分化。

Differentiation of neuroepithelial stem cells into functional dopaminergic neurons in 3D microfluidic cell culture.

机构信息

Luxembourg Centre for Systems Biomedicine, University of Luxembourg, 7 avenue des Hauts-Fourneaux, L-4362 Esch-sur-Alzette, Luxembourg.

出版信息

Lab Chip. 2015 Jun 7;15(11):2419-28. doi: 10.1039/c5lc00180c.

Abstract

A hallmark of Parkinson's disease is the progressive loss of nigrostriatal dopaminergic neurons. We derived human neuroepithelial cells from induced pluripotent stem cells and successfully differentiated them into dopaminergic neurons within phase-guided, three-dimensional microfluidic cell culture bioreactors. After 30 days of differentiation within the microfluidic bioreactors, in situ morphological, immunocytochemical and calcium imaging confirmed the presence of dopaminergic neurons that were spontaneously electrophysiologically active, a characteristic feature of nigrostriatal dopaminergic neurons in vivo. Differentiation was as efficient as in macroscopic culture, with up to 19% of differentiated neurons immunoreactive for tyrosine hydroxylase, the penultimate enzyme in the synthesis of dopamine. This new microfluidic cell culture model integrates the latest innovations in developmental biology and microfluidic cell culture to generate a biologically realistic and economically efficient route to personalised drug discovery for Parkinson's disease.

摘要

帕金森病的一个标志是黑质纹状体多巴胺能神经元的进行性丧失。我们从诱导多能干细胞中分离出神经上皮细胞,并在相控、三维微流控细胞培养生物反应器中成功将其分化为多巴胺能神经元。在微流控生物反应器中分化 30 天后,原位形态学、免疫细胞化学和钙成像证实存在自发电生理活性的多巴胺能神经元,这是体内黑质纹状体多巴胺能神经元的一个特征。分化效率与宏观培养相当,多达 19%的分化神经元对酪氨酸羟化酶呈免疫反应性,酪氨酸羟化酶是多巴胺合成的倒数第二酶。这种新的微流控细胞培养模型集成了发育生物学和微流控细胞培养的最新创新,为帕金森病的个性化药物发现提供了一种具有生物学真实性和经济高效性的途径。

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