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In Vitro Differentiation of Neural Stem Cells Derived From Human Olfactory Bulb Into Dopaminergic-Like Neurons Publisher Pubmed



Alizadeh R1, 2 ; Hassanzadeh G3 ; Joghataei MT1, 4 ; Soleimani M1, 4 ; Moradi F1, 4 ; Mohammadpour S1, 4, 5 ; Ghorbani J6 ; Safavi A6 ; Sarbishegi M7 ; Pirhajati Mahabadi V2, 4 ; Alizadeh L8 ; Hadjighassem M9, 10
Authors
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Authors Affiliations
  1. 1. Cellular and Molecular Research Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
  2. 2. ENT and Head & Neck Research Center and Department, Hazrat Rasoul Akram Hospital, Iran University of Medical Sciences (IUMS), Tehran, Iran
  3. 3. Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Anatomy, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Anatomy, School of Medicine, Ilam University of Medical Sciences, Ilam, Iran
  6. 6. Organ Procurement and Transplant Unit (OPTU), Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  7. 7. Department of Anatomy, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran
  8. 8. Shefa Neuroscience Research Center, Khatam-Alanbia Hospital, Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran, Iran
  9. 9. Brain and Spinal Cord Injury Research Center, Imam Khomeinin Hospital, Tehran University of Medical Sciences, Blv Keshavarz, Tehran, 1419733141, Iran
  10. 10. School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran

Source: European Journal of Neuroscience Published:2017


Abstract

This study describes a new accessible source of neuronal stem cells that can be used in Parkinson's disease cell transplant. The human olfactory bulb contains neural stem cells (NSCs) that are responsible for neurogenesis in the brain and the replacement of damaged cellular components throughout life. NSCs are capable of differentiating into neuronal and glial cells. We isolated NSCs from the olfactory bulb of brain-death donors and differentiated them into dopaminergic neurons. The olfactory bulb tissues obtained were cultured in Dulbecco's modified Eagle's medium/nutrient mixture F12, B27 supplemented with basic fibroblast growth factor, epidermal growth factor and leukemia inhibitory factor. The NSCs and proliferation markers were assessed. The multipotentiality of olfactory bulb NSCs was demonstrated by their capacity to differentiate into neurons, oligodendrocytes and astrocytes. To generate dopaminergic neurons, olfactory bulb NSCs were differentiated in neurobasal medium, supplemented with B27, and treated with sonic hedgehog, fibroblast growth factor 8 and glial cell-derived neurotrophic factor from the 7th to the 21st day, followed by detection of dopaminergic neuronal markers including tyrosine hydroxylase and aromatic l-amino acid decarboxylase. The cells were expanded, established in continuous cell lines and differentiated into the two classical neuronal phenotypes. The percentage of co-positive cells (microtubule-associated protein 2 and tyrosine hydroxylase; aromatic l-amino acid decarboxylase and tyrosine hydroxylase) in the treated cells was significantly higher than in the untreated cells. These results illustrate the existence of multipotent NSCs in the adult human olfactory bulb that are capable of differentiating toward putative dopaminergic neurons in the presence of trophic factors. Taken together, our data encourage further investigations of the possible use of olfactory bulb NSCs as a promising cell-based therapeutic strategy for Parkinson's disease. © 2016 Federation of European Neuroscience Societies and John Wiley & Sons Ltd