Soheilifar Mohammad Hasan, Javeri Arash, Amini Hossein, Taha Masoumeh Fakhr
1 Department of Stem Cells and Regenerative Medicine, Institute for Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB) , Tehran, Iran .
2 Department of Pharmacology, Neuroscience Research Center, Golestan University of Medical Sciences , Gorgan, Iran .
Rejuvenation Res. 2018 Aug;21(4):360-368. doi: 10.1089/rej.2017.1994. Epub 2018 Mar 12.
Several studies have demonstrated the differentiation of human adipose tissue-derived stem cells (hADSCs) to neuronal and glial phenotypes, but directing the fate of these cells toward dopaminergic neurons has not been frequently reported. The aim of this study was to investigate dopaminergic specification of hADSCs in vitro. ADSCs were isolated from subcutaneous abdominal adipose tissue and were characterized. For dopaminergic differentiation, a cocktail of sonic hedgehog, fibroblast growth factor 8, basic fibroblast growth factor, and brain-derived neurotrophic factor were used under a low serum condition. As the control group, the ADSCs were cultured under the same low serum condition without the dopaminergic cocktail. At the end of differentiation period, the cells expressed neuron-specific markers, NES, NSE, and NEFL, and dopaminergic markers, EN1, NURR1, PITX3, VMAT2, TH, and GIRK2 genes. TH, NURR1, and EN1 mRNAs were upregulated in the dopaminergic group compared with the control group. NEFL and TH proteins were also expressed in the differentiated cells. A total of 27.9% of the cells differentiated in dopaminergic induction medium showed positive staining for TH protein. Based on reversed-phase high-performance liquid chromatography analysis, the differentiated cells released a significant amount of dopamine in response to KCl-induced depolarization. In conclusion, results of this study indicate that hADSCs can be induced by a growth factor cocktail to produce dopamine secreting cells with possible applications for future cell replacement therapy of Parkinson's disease.
多项研究已证实人脂肪组织来源的干细胞(hADSCs)可分化为神经元和神经胶质细胞表型,但将这些细胞的命运导向多巴胺能神经元的报道并不常见。本研究的目的是在体外研究hADSCs的多巴胺能定向分化。从腹部皮下脂肪组织中分离出ADSCs并进行鉴定。对于多巴胺能分化,在低血清条件下使用音猬因子、成纤维细胞生长因子8、碱性成纤维细胞生长因子和脑源性神经营养因子的混合物。作为对照组,ADSCs在相同的低血清条件下培养,但不添加多巴胺能混合物。在分化期结束时,细胞表达神经元特异性标志物NES、NSE和NEFL,以及多巴胺能标志物EN1、NURR1、PITX3、VMAT2、TH和GIRK2基因。与对照组相比,多巴胺能组中TH、NURR1和EN1 mRNA上调。分化细胞中也表达NEFL和TH蛋白。在多巴胺能诱导培养基中分化的细胞中,共有27.9%的细胞对TH蛋白呈阳性染色。基于反相高效液相色谱分析,分化细胞在KCl诱导的去极化反应中释放出大量多巴胺。总之,本研究结果表明,hADSCs可被生长因子混合物诱导产生分泌多巴胺的细胞,可能为未来帕金森病的细胞替代治疗提供应用。