| Literature DB >> 30552942 |
Rafieh Alizadeh1, Seyed Kamran Kamrava1, Zohreh Bagher1, Mohammad Farhadi1, Masoumeh Falah1, Fatemeh Moradi2, Mahdi Eskandarian Boroujeni3, Maryam Soleimani4, Ahmadreza Kamyab5, Ali Komeili6.
Abstract
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.Entities:
Keywords: Dopamine producing cells; Dopaminergic neuron-like cells; Human olfactory mucosa; In vitro differentiation; Olfactory ecto-mesenchymal stem cells; Parkinson’s disease
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Year: 2018 PMID: 30552942 DOI: 10.1016/j.neulet.2018.12.011
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046