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Human Dental Pulp Stem Cells Differentiate into Oligodendrocyte Progenitors Using the Expression of Olig2 Transcription Factor

机译:使用olig2转录因子的表达,人牙髓干细胞分化为少突胶质细胞祖细胞祖细胞

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The helix-loop-helix transcription factor Olig2 is essential for lineage determination of oligodendrocytes. Differentiation of stem cells into oligodendrocytes and transplanting them is a novel strategy for the repair of different demyelination diseases. Dental pulp stem cells (DPSCs) are of great interest in regenerative medicine due to their potential for repairing damaged tissues. In this study, DPSCs were isolated from human third molars and transfected with the human Olig2 gene as a differentiation inducer for the oligodendrogenic pathway. Following the differentiation procedure, the expression of Sox2, NG2, PDGFR alpha, Nestin, MBP, Olig2, Oct4, glial fibrillary acidic protein and A2B5 as stage-specific markers was studied by real-time RT-qPCR, immunocytochemistry and Western blot analysis. The cells were transplanted into a mouse model of local sciatic damage by lysolecithin as a model for demyelination. Oligodendrocyte progenitor cells (OPCs) actively remyelinated and recovered the lysolecithin-induced damages in the sciatic nerve as revealed by treadmill exercise, the von Frey filament test and hind paw withdrawal in response to a thermal stimulus. Recovery of behavioral reflexes occurred 2-6 weeks after OPC transplantation. The results demonstrate that the expression of Olig2 in DPSCs reduces the expression of stem cell markers and induces the development of oligodendrocyte progenitors as revealed by the emergence of oligodendrocyte markers. DPSCs could be programmed into oligodendrocyte progenitors and considered as a simple and valuable source for the cell therapy of neurodegenerative diseases. (C) 2015 S. Karger AG, Basel
机译:螺旋环 - 螺旋转录因子OLIG2对于少突胚细胞的谱系确定是必不可少的。干细胞将干细胞分化为少突胶质细胞并移植它们是修复不同脱髓鞘疾病的新策略。由于它们的修复受损组织的可能性,牙齿纸浆干细胞(DPSC)对再生药物具有很大的兴趣。在该研究中,从人第三磨牙中分离DPSC,并用人寡核苷酸转染作为寡突型途径的分化诱导剂。通过实时RT-QPCR,免疫细胞化学和Western印迹分析,研究了在分化过程中,通过实时RT-QPCR,免疫细胞化学和Western印迹分析研究了SOX2,NG2,PDGFRα,巢蛋白,MBP,OLIG2,OCT4,胶质纤维酸性酸性蛋白质和A2B5作为特异性标记物。将细胞移植到通过溶血化素的局部坐骨损伤的小鼠模型中作为脱髓鞘的模型。少压肾细胞祖细胞(OPCs)主动重新键入并回收硅藻土诱导的坐骨神经中的血液神经损伤,如跑步机锻炼所揭示,von Frey灯丝试验和后爪响应热刺激。 OPC移植后2-6周的行为反射恢复。结果表明,DPSCS中的OLIG2的表达降低了干细胞标志物的表达,并诱导少突胶质细胞标记物的出现揭示的少突胚细胞祖细胞的发育。 DPSC可以被编程到少突胶质细胞祖细胞中,并被认为是神经变性疾病细胞治疗的简单且有价值的源。 (c)2015年S. Karger AG,巴塞尔

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