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人胚胎干细胞来源的神经祖细胞与静电纺丝纳米纤维表面在体外的相互作用。

Interactions of human embryonic stem cell-derived neural progenitors with an electrospun nanofibrillar surface in vitro.

作者信息

Rahjouei Ali, Kiani Sahar, Zahabi Azadeh, Mehrjardi Narges Zare, Hashemi Mehrdad, Baharvand Hossein

机构信息

Department of Stem Cells and Developmental Biology, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.

出版信息

Int J Artif Organs. 2011 Jul;34(7):559-70. doi: 10.5301/IJAO.2011.8511.

Abstract

Stem cell technology combined with nano-scaffold surfaces provides a new tool for better induction involved in cell lineage differentiations and therefore for central nervous system repair. This study was undertaken to investigate appropriate neural cell-substrate interactions. Neural progenitors (NPs) were established from human embryonic stem cells (hESCs), as a first step, using an adherent system and a defined medium supplemented with a combination of factors. Next, the behavior of hESC-derived NPs (hESC-NPs) was evaluated on a synthetic, randomly oriented, three-dimensional nanofibrillar matrix composed of electrospun polyamide nanofibers (Ultra-Web™) using a variety of experimental approaches. We have demonstrated that homogenous, expandable, and self-renewable NPs can be easily generated from hESCs; they can express related markers Nestin, Sox1, and Pax6; and they can undergo multipotency differentiation to neurons and glials. Functionally, NPs cultured on nanofibers demonstrated an increase in the rate of migration, proliferation, morphology, and neurite length when compared with NPs cultured on two-dimensional culture surfaces. The results suggest that topographical features of the extracellular matrix of the cell environment have paved the way for a better understanding of human neuronal development, thus allowing for future clinical applications.

摘要

干细胞技术与纳米支架表面相结合,为更好地诱导细胞谱系分化以及中枢神经系统修复提供了一种新工具。本研究旨在探究合适的神经细胞与基质的相互作用。第一步,使用贴壁系统和添加多种因子的限定培养基,从人类胚胎干细胞(hESC)中建立神经祖细胞(NP)。接下来,采用多种实验方法,在由静电纺丝聚酰胺纳米纤维(Ultra-Web™)构成的合成、随机取向的三维纳米纤维基质上评估hESC来源的NP(hESC-NP)的行为。我们已经证明,hESC能够轻松产生均匀、可扩增且自我更新的NP;它们能够表达相关标志物巢蛋白、Sox1和Pax6;并且能够向神经元和神经胶质细胞进行多能分化。在功能上,与在二维培养表面培养的NP相比,在纳米纤维上培养的NP在迁移率、增殖、形态和神经突长度方面均有所增加。结果表明,细胞环境的细胞外基质的拓扑特征为更好地理解人类神经元发育铺平了道路,从而为未来的临床应用提供了可能。

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