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Combined Effects of Rat Schwann Cells and 17Β-Estradiol in a Spinal Cord Injury Model Publisher Pubmed



Namjoo Z1 ; Moradi F1, 2 ; Aryanpour R3 ; Piryaei A4, 5 ; Joghataei MT1, 2 ; Abbasi Y1 ; Hosseini A1 ; Hassanzadeh S1 ; Taklimie FR6 ; Beyer C6 ; Zendedel A6, 7
Authors
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Authors Affiliations
  1. 1. Department of Anatomy, Faculty of Medicine, Iran University of Medical Sciences, Hemmat Campus, Tehran, Iran
  2. 2. Cellular and Molecular Research Center, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Anatomy, Faculty of Medicine, Yasuj University of Medical Sciences, Yasuj, Iran
  4. 4. Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  5. 5. Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  6. 6. Institute of Neuroanatomy, RWTH Aachen University, Aachen, 52074, Germany
  7. 7. Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Source: Metabolic Brain Disease Published:2018


Abstract

Spinal cord injury (SCI) is a devastating traumatic event which burdens the affected individuals and the health system. Schwann cell (SC) transplantation is a promising repair strategy after SCI. However, a large number of SCs do not survive following transplantation. Previous studies demonstrated that 17β-estradiol (E2) protects different cell types and reduces tissue damage in SCI experimental animal model. In the current study, we evaluated the protective potential of E2 on SCs in vitro and investigated whether the combination of hormonal and SC therapeutic strategy has a better effect on the outcome after SCI. Primary SC cultures were incubated with E2 for 72 h. In a subsequent experiment, thoracic contusion SCI was induced in male rats followed by sustained administration of E2 or vehicle. Eight days after SCI, DiI-labeled SCs were transplanted into the injury epicenter in vehicle and E2-treated animals. The combinatory regimen decreased neurological and behavioral deficits and protected neurons and oligodendrocytes in comparison to vehicle rats. Moreover, E2 and SC significantly decreased the number of Iba-1+ (microglia) and GFAP + cells (astrocyte) in the SCI group. In addition, we found a significant reduction of mitochondrial fission-markers (Fis1) and an increase of fusion-markers (Mfn1 and Mfn2) in the injured spinal cord after E2 and SC treatment. These data demonstrated that E2 protects SCs against hypoxia-induced SCI and improves the survival of transplanted SCs. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.
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