O13: Human Neural Stem/Progenitor Cells Derived from Epileptic Human Brain in A Self-Assembling Peptide Nanoscaffold Attenuates Neuroinlammation in Traumatic Brain Injury in Rats

Authors

  • Ali Gorji a. Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran b. Department of Neuroscience, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran c. Department of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany d. Epilepsy Research Center, Westfälische Wilhelms-Universität Münster, Münster, Germany
  • Ali Jahanbazi Jahan-Abad a. Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran b. Department of Clinical Biochemistry, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Hassan Hosseini Ravandi Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran
  • Maryam Khaleghi Ghadiri Department of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany
  • Sajad Sahab Negah a. Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran b. Department of Neuroscience, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
  • Sedigheh Ghasemi Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran
  • Walter Stummer Department of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany
Abstract:

Traumatic brain injury (TBI) is a disruption in the brain functions following a head trauma. Cell therapy may provide a promising treatment for TBI. Human neural stem cells cultured in self-assembling peptide scaffolds have been proposed as a potential novel method for cell replacement treatment after TBI. In the present study, we accessed the effects of human neural stem/progenitor cells (hNS/PCs) derived from epileptic human brain and human adipose-derived stromal/stem cells (hADSCs) cultured in the RADA16 on brain function after TBI. hNS/PCs were isolated from patients with medically intractable epilepsy undergone epilepsy surgery. hNS/PCs and hADSCs have the potential for proliferation and differentiation into both neuronal and glial lineages. Transplantation of hNS/PCs and hADSCs encapsulated in the PM inhibited neuroinflammation, and reduced the reactive gliosis at the injury site of TBI. The data suggest the transplantation of human stem cells encapsulated in the PM as a hopeful treatment option for cell therapy in TBI.  

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Journal title

volume 6  issue 2

pages  13- 13

publication date 2018-04

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