Efficient generation of dopaminergic-like neurons by overexpression of Nurr1 and Pitx3 in mouse induced Pluripotent Stem Cells

被引:15
作者
Salemi, Salemeh [1 ]
Baktash, Parvaneh [1 ]
Rajaei, Bahareh [2 ]
Noori, Mehri [1 ]
Amini, Hossein [3 ]
Shamsara, Mehdi [1 ]
Massumi, Mohammad [4 ,5 ]
机构
[1] Natl Inst Genet Engn & Biotechnol, Natl Ctr Transgen Mouse Res, Tehran, Iran
[2] Natl Inst Genet Engn & Biotechnol, Dept Med Genet, Tehran, Iran
[3] Golestan Univ Med Sci, Neurosci Res Ctr, Dept Pharmacol, Gorgan, Iran
[4] Univ Toronto, Dept Physiol, Toronto, ON, Canada
[5] Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON, Canada
关键词
Dopaminergic neurons; Induced-pluripotent stem cells; Nurr1; Parkinson's disease; Pitx3; TRANSCRIPTION FACTOR PITX3; PARKINSONS-DISEASE; IPS CELLS; HUMAN ES; DIFFERENTIATION; MIDBRAIN; EXPRESSION; PHENOTYPE; THERAPY; MODEL;
D O I
10.1016/j.neulet.2016.05.032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Parkinson's disease (PD) is a neurodegenerative disorder, in which the nigro-striatal Dopaminergic (DAergic) neurons are selectively lost. Treatment of neurodegenerative diseases with Pluripotent Stem Cells (PSCs) is a big interest in cell therapy. Here, we used induced Pluripotent Stem Cells (iPSCs) expressing two master Dopaminergic (DAergic) transcription factors, i.e. Nurr1 and Pitx3, to generate functional in vitro DAergic-like neurons. After establishment and characterization of Doxycycline-inducible iPSCs from mouse fibroblasts, the cells were transduced by NURR1- and PITX3-harboring lentiviruses. The Nurr1/Pitx3-iPSCs were differentiated through a five-stage protocol to generate DAergic-like neurons. The results confirmed the efficient expression of DAergic neuron markers in the end of protocol. Beside, the generated cells could exclusively synthesize and secrete Dopamine in response to secretagogues. In conclusion, overexpression of Nurr1 and Pitx3 in iPSCs could efficiently program iPSCs into functional DAergic-like neurons. This finding may have an impact on future stem cell therapy of PD. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:126 / 134
页数:9
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