出生后星形胶质细胞促进成人骨髓来源干细胞的神经诱导。

Alexis Joannides, Phil Gaughwin, Mike Scott, Suzanne Watt, Alastair Compston, Siddharthan Chandran
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引用次数: 38

摘要

神经干细胞(NSCs)由于其作为神经退行性疾病的药物筛选或基于细胞的治疗的确定细胞来源的潜力而引起了相当大的兴趣。伦理和实际考虑限制了人类胎儿来源的神经组织的可用性,并强调需要考虑人类NSCs的替代来源。由于其现成的可用性,易于扩展的能力,以及神经电位的报道,骨髓来源的群体已经成为关于其潜在临床应用的激烈研究的焦点。然而,最近发现的自发细胞融合和有限的神经元分化已经缓和了最初的乐观。在这项研究中,我们证明了成人骨髓间充质细胞的单克隆神经和中胚层潜能。关键的是,我们发现,在出生后海马星形胶质细胞条件培养基中依次使用有丝分裂原表皮生长因子(EGF)和成纤维细胞生长因子-2 (FGF-2),可显著促进骨髓前体神经丝(+)/ β -微管蛋白(+)细胞的生成。从易于获得的成人自体来源中产生几乎无限数量的神经前体的能力为进一步研究提供了平台,并可能具有重要的治疗意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Postnatal astrocytes promote neural induction from adult human bone marrow-derived stem cells.

Neural stem cells (NSCs) have generated considerable interest because of their potential as a source of defined cells for drug screening or cell-based therapies for neurodegenerative diseases. Ethical and practical considerations limit the availability of human fetal-derived neural tissue and highlight the need to consider alternative sources of human NSCs. Because of their ready availability, their ability to be easily expanded, and reports of neural potential, bone marrow-derived populations have become the focus of intense study with regard to their potential clinical utility. However, recent identification of spontaneous cell fusion and limited neuronal differentiation has tempered initial optimism. In this study, we demonstrate the monoclonal neural and mesodermal potential of adult human bone marrow mesenchymal cells. Critically, we show that sequential treatment with the mitogens epidermal growth factor (EGF) and fibroblast growth factor-2 (FGF-2) followed by postnatal hippocampal astrocyte conditioned medium significantly promotes the generation of neurofilament(+)/beta-tubulin(+) cells from bone marrow precursors. The ability to generate almost limitless numbers of neural precursors from a readily accessible autologous adult human source provides a platform for further studies and potentially has important therapeutic implications.

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