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Induced in Vitro Differentiation of Neural-Like Cells From Human Exfoliated Deciduous Teeth-Derived Stem Cells Publisher Pubmed



Nourbakhsh N1 ; Soleimani M2 ; Taghipour Z2 ; Karbalaie K3 ; Mousavi S4 ; Talebi A5 ; Nadali F5 ; Tanhaei S3 ; Kiyani GA1 ; Nematollahi M3 ; Rabiei F1 ; Mardani M2 ; Bahramiyan H2 ; Torabinejad M6 Show All Authors
Authors
  1. Nourbakhsh N1
  2. Soleimani M2
  3. Taghipour Z2
  4. Karbalaie K3
  5. Mousavi S4
  6. Talebi A5
  7. Nadali F5
  8. Tanhaei S3
  9. Kiyani GA1
  10. Nematollahi M3
  11. Rabiei F1
  12. Mardani M2
  13. Bahramiyan H2
  14. Torabinejad M6
  15. Nasresfahani MH3
  16. Baharvand H7, 8
Show Affiliations
Authors Affiliations
  1. 1. Pediatric Department, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, P.O. Box: 8174673461, Iran
  2. 2. Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of Cell and Molecular Biology, Royan Institute for Animal Biotechnology, Isfahan, Iran
  4. 4. Endodentic Department, School of Dentistry, Torabinejad Dental Center, Isfahan University, Isfahan, Iran
  5. 5. Pathology Department, Faculty of Medical Sciences, Isfahan University, Isfahan, Iran
  6. 6. Endodentic Department, Lumalinda University, United States
  7. 7. Department of Stem Cells and Developmental Biology, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, P.O. Box 19395-4644, Iran
  8. 8. Department of Developmental Biology, University of Science and Culture, ACECR, Tehran, Iran

Source: International Journal of Developmental Biology Published:2011


Abstract

Stem cells from human exfoliated deciduous teeth (SHED) are highly proliferative, clonogenic and multipotent stem cells with a neural crest cell origin. Additionally, they can be collected with minimal invasiveness in comparison with other sources of mesenchymal stem cells (MSCs). Therefore, SHED could be a desirable option for potential therapeutic applications. In this study, SHEDs were established from enzyme-disaggregated deciduous dental pulp obtained from 6 to 9 year-old children. The cells had typical fibroblastoid morphology and expressed antigens characteristic of MSCs, STRO1, CD146, CD45, CD90, CD106 and CD166, but not the hematopoietic and endothelial markers, CD34 and CD31, as assessed by FACS analysis. Differentiation assessment revealed a strong osteogenic and adipogenic potential of SHEDs. In order to further evaluate the in vitro differentiation potential of SHED into neural cells, a simple short time growth factormediated induction was used. Immunofluorescence staining and flow cytometric analysis revealed that SHED rapidly expressed nestin and β-III tubulin, and later expressed intermediate neural markers. In addition, the intensity and percentages of nestin and β-III tubulin and mature neural markers (PSA-NCAM, NeuN, Tau, TH, or GFAP) increased significantly following treatment. Moreover, RT-PCR and Western blot analyses showed that the neural markers were strongly upregulated after induction. In conclusion, these results provide evidence that SHED can differentiate into neural cells by the expression of a comprehensive set of genes and proteins that define neural-like cells in vitro. SHED cells might be considered as new candidates for the autologous transplantation of a wide variety of neurological diseases and neurotraumatic injuries. © 2011 UBC Press.
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