Neural Stem Cell Research Lab, Research Department, National Neuroscience Institute, Singapore.
Stem Cell Group, Bioprocessing Technology Institute, Agency for Science, Technology and Research, Singapore.
Stem Cells Transl Med. 2017 Sep;6(9):1803-1814. doi: 10.1002/sctm.16-0470. Epub 2017 Jun 26.
Recent reports have indicated human embryonic stem cells-derived midbrain dopamine (mDA) neurons as proper cell resources for use in Parkinson's disease (PD) therapy. Nevertheless, no detailed and systematic study has been conducted to identify which differentiation stages of mDA cells are most suitable for transplantation in PD therapy. Here, we transplanted three types of mDA cells, DA progenitors (differentiated in vitro for 16 days [D16]), immature DA neurons (D25), and DA neurons (D35), into PD mice and found that all three types of cells showed high viability and strong neuronal differentiation in vivo. Both D25 and D35 cells showed neuronal maturation and differentiation toward TH cells and, accordingly, satisfactory behavioral functional recovery. However, transplanted D16 cells were less capable of producing functional recovery. These findings provide a valuable guideline for standardizing the differentiation stage of the transplantable cells used in clinical cell therapy for PD. Stem Cells Translational Medicine 2017;6:1803-1814.
最近的报告表明,人类胚胎干细胞衍生的中脑多巴胺(mDA)神经元是用于帕金森病(PD)治疗的合适细胞资源。然而,目前还没有进行详细和系统的研究来确定 mDA 细胞的哪个分化阶段最适合用于 PD 治疗的移植。在这里,我们将三种类型的 mDA 细胞,即 DA 祖细胞(体外分化 16 天[D16])、未成熟的 DA 神经元(D25)和 DA 神经元(D35),移植到 PD 小鼠体内,发现所有三种类型的细胞在体内均具有高活力和强神经元分化能力。D25 和 D35 细胞均显示出向 TH 细胞的神经元成熟和分化,因此表现出令人满意的行为功能恢复。然而,移植的 D16 细胞产生功能恢复的能力较弱。这些发现为规范用于 PD 临床细胞治疗的可移植细胞的分化阶段提供了有价值的指导。《干细胞转化医学》2017;6:1803-1814.