Human olfactory stem cells: As a promising source of dopaminergic neuron-like cells for treatment of Parkinson's disease

被引:36
作者
Alizadeh, Rafieh [1 ]
Kamrava, Seyed Kamran [1 ]
Bagher, Zohreh [1 ]
Farhadi, Mohammad [1 ]
Falah, Masoumeh [1 ]
Moradi, Fatemeh [2 ]
Boroujeni, Mahdi Eskandarian [3 ]
Soleimani, Maryam [4 ]
Kamyab, Ahmadreza [5 ]
Komeili, Ali [6 ]
机构
[1] Iran Univ Med Sci, Hazrat Rasoul Akram Hosp, Senses Inst 5, ENT & Head & Neck Res Ctr & Dept, Tehran, Iran
[2] Iran Univ Med Sci, Sch Med, Dept Anat, Tehran, Iran
[3] Natl Inst Genet Engn & Biotechnol, Fac Med Biotechnol, Dept Stem Cells & Regenerat Med, Tehran, Iran
[4] Univ Social Welf & Rehabil Sci, Dept Basic Sci, Tehran, Iran
[5] Mol Diagnost Dept, Noor Pathobiol Lab, Tehran, Iran
[6] Islamic Azad Univ, Sci & Res Branch, Appl Biophoton Res Ctr, Tehran, Iran
关键词
Dopaminergic neuron-like cells; Human olfactory mucosa; Olfactory ecto-mesenchymal stem cells; In vitro differentiation; Dopamine producing cells; Parkinson's disease; IN-VITRO; DIFFERENTIATION; EXPRESSION;
D O I
10.1016/j.neulet.2018.12.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The production of dopaminergic (DA) neurons from stem cells holds a great promise for future clinical treatment of neurodegenerative diseases, such as Parkinson's disease (PD). Olfactory ecto-mesenchymal stem cells (OE-MSCs) derived from the adult human olfactory mucosa can be easily isolated and expanded in culture while maintaining their immense plasticity. In addition to reduced ethical concerns, OE-MSCs could be transplanted across allogeneic barriers, making them desirable stem cells for clinical applications. The goal of this study was to define the potentiality of human olfactory mucosa-derived MSCs aimed at differentiation into DA neuron-like cells. OE-MSCs were induced to differentiate to DA neuron-like cells in vitro by using sonic hedgehog (SHH), fibroblast growth factor 8 (FGF8), basic fibroblast growth factor (bFGF), Glial cell line-derived neurotrophic factor (GDNF) and brain derived neurotrophic factor (BDNF). Then the differentiated neurons were characterized for expression of DA neuron markers by Real-time PCR, immunocytochemistry and flow cytometry. Our findings showed that differentiated OE-MSCs could significantly express DA neuron markers at mRNA and protein levels along with dopamine release 12 days post-differentiation. These results support the viability and feasibility of using OE-MSCs as a source of in vitro generated DA neuron-like cells for treatment of DA disorders namely PD.
引用
收藏
页码:52 / 59
页数:8
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