Institute of Genetic Medicine, Newcastle University, Centre for Life, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK.
Stem Cell Rev Rep. 2014 Apr;10(2):316-26. doi: 10.1007/s12015-013-9493-9.
Here we provide a protocol for the directed differentiation of hEPI-NCSC into midbrain dopaminergic neurons, which degenerate in Parkinson's disease. hEPI-NCSC are neural crest-derived multipotent stem cells that persist into adulthood in the bulge of hair follicles. The experimental design is distinctly different from conventional protocols for embryonic stem cells and induced pluripotent stem (iPS) cells. It includes pre-differentiation of the multipotent hEPI-NCSC into neural stem cell-like cells, followed by ventralizing, patterning, continued exposure to the TGFβ receptor inhibitor, SB431542, and at later stages of differentiation the presence of the WNT inhibitor, IWP-4. All cells expressed A9 midbrain dopaminergic neuron progenitor markers with gene expression levels comparable to those in normal human substantia nigra. The current study shows for the first time that virtually homogeneous populations of dopaminergic neurons can be derived ex vivo from somatic stem cells without the need for purification, with useful timeliness and high efficacy. This novel development is an important first step towards the establishment of fully functional dopaminergic neurons from an ontologically relevant stem cell type, hEPI-NCSC.
在这里,我们提供了一个方案,用于将人表皮神经嵴干细胞(hEPI-NCSC)定向分化为中脑多巴胺能神经元,这些神经元在帕金森病中会退化。hEPI-NCSC 是神经嵴衍生的多能干细胞,在毛囊的隆起处存在于成年期。该实验设计明显不同于传统的胚胎干细胞和诱导多能干细胞(iPS)细胞方案。它包括将多能 hEPI-NCSC 预先分化为神经干细胞样细胞,然后进行腹侧化、模式化,继续暴露于 TGFβ 受体抑制剂 SB431542,在分化的后期阶段存在 WNT 抑制剂 IWP-4。所有细胞都表达 A9 中脑多巴胺能神经元祖细胞标记物,其基因表达水平与正常人类黑质相当。本研究首次表明,实际上可以从体细胞干细胞中体外衍生出几乎同质的多巴胺能神经元,而无需纯化,具有有用的时效性和高效性。这一新颖的发展是朝着建立来自于与本体论相关的干细胞类型 hEPI-NCSC 的完全功能性多巴胺能神经元迈出的重要第一步。