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The Restorative Effect of Human Amniotic Fluid Stem Cells on Spinal Cord Injury Publisher Pubmed



Ataei ML1, 2 ; Karimipour M2 ; Shahabi P3, 4 ; Pashaeiasl R5 ; Ebrahimie E6, 7, 8, 9 ; Pashaiasl M2, 10, 11, 12
Authors
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Authors Affiliations
  1. 1. Neuroscience Research Center, Tabriz University of Medical Sciences, Tabriz, 5166614766, Iran
  2. 2. Department of Anatomical Sciences, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, 5166614766, Iran
  3. 3. Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, 5166614766, Iran
  4. 4. Department of Physiology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, 5166614766, Iran
  5. 5. Department of Clinical Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, 1417653911, Iran
  6. 6. School of Life Sciences, College of Science, Health and Engineering, La Trobe University, Melbourne, 3086, VIC, Australia
  7. 7. Genomics Research Platform, Research & Industry Engagement, La Trobe University, Melbourne, 3086, VIC, Australia
  8. 8. School of Animal and Veterinary Sciences, The University of Adelaide, Adelaide, 5371, SA, Australia
  9. 9. School of BioSciences, Faculty of Science, The University of Melbourne, Melbourne, 3010, VIC, Australia
  10. 10. Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, 5166614766, Iran
  11. 11. Department of Reproductive Biology, Faculty of Advanced Medical Science, Tabriz University of Medical Science, Tabriz, 5166614766, Iran
  12. 12. Women’s Reproductive Health Research Center, Tabriz University of Medical Sciences, Tabriz, 5166614766, Iran

Source: Cells Published:2021


Abstract

Spinal cord injury (SCI) is a debilitating condition within the neural system which is clinically manifested by sensory-motor dysfunction, leading, in some cases, to neural paralysis for the rest of the patient’s life. In the current study, mesenchymal stem cells (MSCs) were isolated from the human amniotic fluid, in order to study their juxtacrine and paracrine activities. Flow cytometry analysis was performed to identify the MSCs. A conditioned medium (CM) was collected to measure the level of BDNF, IL-1β, and IL-6 proteins using the ELISA assay. Following the SCI induction, MSCs and CM were injected into the lesion site, and also CM was infused intraperitoneally in the different groups. Two weeks after SCI induction, the spinal cord samples were examined to evaluate the expression of the doublecortin (DCX) and glial fibrillary acid protein (GFAP) markers using immunofluorescence staining. The MSCs’ phenotype was confirmed upon the expression and un-expression of the related CD markers. Our results show that MSCs increased the expression level of the DCX and decreased the level of the GFAP relative to the injury group (p < 0.001). Additionally, the CM promoted the DCX expression rate (p < 0.001) and decreased the GFAP expression rate (p < 0.01) as compared with the injury group. Noteworthily, the restorative potential of the MSCs was higher than that of the CM (p < 0.01). Large-scale meta-analysis of transcriptomic data highlighted PAK5, ST8SIA3, and NRXN1 as positively coexpressed genes with DCX. These genes are involved in neuroactive ligand–receptor interaction. Overall, our data revealed that both therapeutic interventions could promote the regeneration and restoration of the damaged neural tissue by increasing the rate of neuroblasts and decreasing the astrocytes. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.