Combination of Stem Cell Mobilized by Granulocyte-Colony Stimulating Factor and Human Umbilical Cord Matrix Stem Cell: Therapy of Traumatic Brain Injury in Rats

Authors

  • Asghar Ebrahimi Department of Biotechnology and Bioscience, Milano-Bicocca University, Milan, Italy
  • Bahareh Laribi Department of Immunology, Tehran University of Medical Sciences, Tehran, Iran
  • Mahdi Tondar Department of Anatomy, Tehran University of Medical Science, Tehran, Iran
  • Mehdi Mehdizadeh Cellular & Molecular Research Center, Tehran University of Medical Sciences, Tehran, Iran|Department of Anatomy, Tehran University of Medical Science, Tehran, Iran
  • Mehrdad Bakhtiary Cellular & Molecular Research Center, Tehran University of Medical Sciences, Tehran, Iran|Department of Anatomy, Tehran University of Medical Science, Tehran, Iran
  • Mohammad Taghi Joghataei Cellular & Molecular Research Center, Tehran University of Medical Sciences, Tehran, Iran|Department of Anatomy, Tehran University of Medical Science, Tehran, Iran
  • Mohsen Marzban Cellular & Molecular Research Center, Tehran University of Medical Sciences, Tehran, Iran|Department of Anatomy, Tehran University of Medical Science, Tehran, Iran
  • Navid Modiry Department of Anatomy, Tehran University of Medical Science, Tehran, Iran
  • Samideh Khoei Cellular & Molecular Research Center, Tehran University of Medical Sciences, Tehran, Iran|Department of Medical Physics, Tehran University of Medical Sciences, Tehran, Iran
  • Soraya Mehrabi Department of physiology, Tehran University of Medical Sciences, Tehran, Iran
Abstract:

Objective(s) Clinical studies of treating traumatic brain injury (TBI) with autologous adult stem cells led us to examine the impression of a combination therapy. This was performed by intravenous injection of human umbilical cord matrix stem cell (hUCMSC-Wharton,s jelly stem cell) with bone marrow cell mobilized by granulocytecolony stimulating factor (G-CSF) in rats injured with cortical compact device. Materials and Methods Adult male Wistar rats (n= 50) were injured with controlled cortical impact device and divided into five groups. All injections were performed 1 day after injury into the tail veins of rats. Neurological functional evaluation of animals was performed before and after injury using modified neurological severity scores (mNSS). Animals were sacrificed 42 days after TBI and brain sections were stained by Brdu immunohistochemistry. Results Statistically significant improvement in functional outcome was observed in treatment groups when compared with control (P< 0.01). mNSS showed no significant differences among the hUCMSC and G-CSF treated groups at any time point (end of trial). Rats with hUCMSC + G-CSF treatment had a significant improvement on mNSS at 5 and 6 week compared to other treatment group (P< 0.01). Conclusion Histological analysis in G-CSF+ hUCMSC treated traumatic rats exhibited significant increase in numbers of Brdu immunoreactive cells in their traumatic core compared with other labeled group.

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Journal title

volume 14  issue 4

pages  327- 339

publication date 2011-07-01

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