Histological and immunohistochemical study of the potential therapeutic impacts of bone marrow mesenchymal stem cells and exosomes for sciatic nerve crush injury model in rats
• 2018
Publication Information
Authors
Nahla El-Eraky El-Azaba, Abeer M. El-Mahalawaya, Ola Mostafaa and Dina Sabry b
Keywords
Not Available
Journal
Not Available
Publisher
Not Available
Volume
Not Available
Issue
Not Available
Pages
Not Available
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
The aim was to evaluate the potential effect of bone marrow-derived mesenchymal stem cells
(BMSC) and BMSC-EX in the sciatic nerve injury. Forty-five rats were divided into four groups, i.e.
Group I control no surgery or treatment, Group II sciatic nerve crush surgery and 1 week postsurgery,
Group III sciatic nerve crush injury was treated with BMSC, and Group IV sciatic nerve
crush injury was treated with BMSC-EX. All animal groups were euthanized 2 weeks after
treatment. Sciatic nerves were examined histologically and immunohistochemically. Group II
showed various histological changes, i.e. vacuolation, degeneration and loss of nerve fibers.
Group II showed a significant increase in collagen fibers, but with significant reduction in osmium
tetroxide (OsO4)-stained myelin sheaths and neurofilament immunostaining compared to Group
I. Group II also revealed distortion and disruption of myelinated nerve fibers. Groups III and IV
showed significant improvement of both histological and immunohistochemical changes in
Group II. BMSC and BMSC-EX were shown to improve axonal regeneration.
(BMSC) and BMSC-EX in the sciatic nerve injury. Forty-five rats were divided into four groups, i.e.
Group I control no surgery or treatment, Group II sciatic nerve crush surgery and 1 week postsurgery,
Group III sciatic nerve crush injury was treated with BMSC, and Group IV sciatic nerve
crush injury was treated with BMSC-EX. All animal groups were euthanized 2 weeks after
treatment. Sciatic nerves were examined histologically and immunohistochemically. Group II
showed various histological changes, i.e. vacuolation, degeneration and loss of nerve fibers.
Group II showed a significant increase in collagen fibers, but with significant reduction in osmium
tetroxide (OsO4)-stained myelin sheaths and neurofilament immunostaining compared to Group
I. Group II also revealed distortion and disruption of myelinated nerve fibers. Groups III and IV
showed significant improvement of both histological and immunohistochemical changes in
Group II. BMSC and BMSC-EX were shown to improve axonal regeneration.
Staff Members - Benha University