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Transplantation of Undifferentiated and Induced Human Exfoliated Deciduous Teeth-Derived Stem Cells Promote Functional Recovery of Rat Spinal Cord Contusion Injury Model Publisher Pubmed



Taghipour Z1, 2 ; Karbalaie K1 ; Kiani A1 ; Niapour A1, 2 ; Bahramian H2 ; Nasresfahani MH1 ; Baharvand H3, 4
Authors
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Authors Affiliations
  1. 1. Department of Cell and Molecular Biology, Cell Science Research Center, Royan Institute for Animal Biotechnology, Isfahan 815896-8433, Iran
  2. 2. Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran
  3. 3. Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, Tehran 19395-4644, Iran
  4. 4. Department of Developmental Biology, University of Science and Culture, ACECR, Tehran, Iran

Source: Stem Cells and Development Published:2012


Abstract

Regarding both the neural crest origin and neuronal potential of stem cells from human exfoliated deciduous teeth (SHED), here, we assessed their potential in addition to neural induced SHED (iSHED) for functional recovery when transplanted in a rat model for acute contused spinal cord injury (SCI). Following transplantation, a significant functional recovery was observed in both groups relative to the vehicle and control groups as determined by the open field locomotor functional test. We also observed that animals that received iSHED were in a better state as compared with the SHED group. Immunohistofluorescence evaluation 5 weeks after transplantation showed neuronal and glial differentiation and limited proliferation in both groups. However, myelin basic protein and chondroitin sulfate proteoglycan NG2-oligodendrocyte markers-were increased and glial fibrillary acidic protein-astrocyte marker-was decreased in the iSHED group in comparison with the SHED group. These findings have demonstrated that transplantation of SHED or its derivatives could be a suitable candidate for the treatment of SCI as well as other neuronal degenerative diseases. © 2012 Mary Ann Liebert, Inc.
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