Author/Authors :
Nazm Bojnordi Maryam نويسنده , Ghasemi Hamidabadi Hatef نويسنده Department of Anatomy, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran , Alizadeh Rafieh نويسنده Department of Anatomy, Tehran University of Medical Sciences, Tehran, IR Iran , Moayeri Ardeshir نويسنده Department of Anatomy, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran. AND Department of Anatomy, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran. Moayeri Ardeshir , Haratizadeh Sara نويسنده Department of Anatomical Sciences, Faculty of Medicine,
Mazandaran University of Medical Sciences, Sari, IR
Iran , Esmaeilnejad-Moghadam Amir نويسنده Department of Anatomy & Cell Biology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran. Esmaeilnejad-Moghadam Amir
Abstract :
Introduction: The nerve fibers in central nervous system are surrounded by myelin sheet which is formed by oligodendrocytes. Cell therapy based on oligodendrocytes and their precursors transplantation can hold a promising alternative treatment for myelin sheet repair in demyelinating diseases.
Methods: Human Dental Pulp Stem Cells (hDPSCs) are noninvasive, autologous and easy available source with multipotency characteristics, so they are in focus of interest in regenerative medicine. In the present study, hDPSCs were differentiated into oligoprogenitor using glial induction media, containing Retinoic Acid (RA), basic Fibroblast Growth Factor (bFGF), Platelet-Derived Growth Factor (PDGF), N2 and B27. The differentiated Oligoprogenitor Cells (OPCs) were evaluated for nestin, Olig2, NG2 and O4 using immunocytochemistry. Also, the expression of nestin, Olig2 and PDGFR-α gens (neuroprogenitor and oligoprogenitor markers) were investigated via RT-PCR technique.
Results: The results indicate that glial differentiation medium induces the generation of oligoprogenitor cells as revealed via exhibition of specific glial markers, including Olig2, NG2 and O4. The expersion of nestin gene (neuroprogenitor marker) and Olig2 and PDGFR-α genes (oligoprogentor markers) were detected in treated hDPSCs at the end of the induction stage.
Conclusion: hDPSCs can be induced to transdifferentiate into oligoprogenitor cells and respond to the routinely applied regents for glial differentiation of mesanchymal stem cells. These data suggest the hDPSCs as a valuable source for cell therapy in neurodegenerative diseases.
