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Preparing Neural Stem/Progenitor Cells in Puramatrix Hydrogel for Transplantation After Brain Injury in Rats: A Comparative Methodological Study Publisher Pubmed



Aligholi H1, 2, 3 ; Rezayat SM4 ; Azari H5, 6 ; Ejtemaei Mehr S4 ; Akbari M7 ; Modarres Mousavi SM1 ; Attari F1, 2 ; Alipour F1 ; Hassanzadeh G7 ; Gorji A1, 8, 9
Authors
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Authors Affiliations
  1. 1. Shefa Neuroscience Research Center, Khatam-al-Anbia Hospital, Tehran, Iran
  2. 2. Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Neuroscience, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
  4. 4. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Neural Stem Cell and Regenerative Neuroscience Laboratory, Department of Anatomical Sciences, School of Medicine, Shiraz, Iran
  6. 6. Shiraz Stem Cell Institute, Shiraz University of Medical Sciences, Shiraz, Iran
  7. 7. Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  8. 8. Department of Neuroscience, Mashhad University of Medical Sciences, Mashhad, Iran
  9. 9. Epilepsy Research Center, Department of Neurosurgery, Department of Neurology, Westfalische Wilhelms-Universitat Munster, Munster, Germany

Source: Brain Research Published:2016


Abstract

Cultivation of neural stem/progenitor cells (NS/PCs) in PuraMatrix (PM) hydrogel is an option for stem cell transplantation. The efficacy of a novel method for placing adult rat NS/PCs in PM (injection method) was compared to encapsulation and surface plating approaches. In addition, the efficacy of injection method for transplantation of autologous NS/PCs was studied in a rat model of brain injury. NS/PCs were obtained from the subventricular zone (SVZ) and cultivated without (control) or with scaffold (three-dimensional cultures; 3D). The effect of different approaches on survival, proliferation, and differentiation of NS/PCs were investigated. In in vivo study, brain injury was induced 45 days after NS/PCs were harvested from the SVZ and phosphate buffered saline, PM, NS/PCs, or PM+NS/PCs were injected into the brain lesion. There was an increase in cell viability and proliferation after injection and surface plating of NS/PCs compared to encapsulation and neural differentiation markers were expressed seven days after culturing the cells. Using injection method, transplantation of NS/PCs cultured in PM resulted in significant reduction of lesion volume, improvement of neurological deficits, and enhancement of surviving cells. In addition, the transplanted cells could differentiate in to neurons, astrocytes, or oligodendrocytes. Our results indicate that the injection and surface plating methods enhanced cell survival and proliferation of NS/PCs and suggest the injection method as a promising approach for transplantation of NS/PCs in brain injury. © 2016 Elsevier B.V. All rights reserved.