Biodegradable chitin conduit tubulation combined with bone marrow mesenchymal stem cell transplantation for treatment of spinal cord injury by reducing glial scar and cavity formation

We examined the restorative effect of modified biodegradable chitin conduits in combination with bone marrow mesenchymal stem cell transplantation after right spinal cord hemisection injury. Immunohistochemical staining revealed that biological conduit sleeve bridging reduced glial scar formation an...

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Published inNeural regeneration research Vol. 10; no. 1; pp. 104 - 111
Main Authors Xue, Feng, Wu, Er-jun, Zhang, Pei-xun, A, Li-ya, Kou, Yu-hui, Yin, Xiao-feng, Han, Na
Format Journal Article
LanguageEnglish
Published India Medknow Publications and Media Pvt. Ltd 2015
Medknow Publications & Media Pvt. Ltd
Department of Trauma and 0rthopedics, Peking University People’s Hospital, Beijing, China%Graduate School of Shanxi Medical University, Taiyuan, Shanxi Province, China%Central Laboratory, Peking University People’s Hospital, Beijing, China
Medknow Publications & Media Pvt Ltd
Wolters Kluwer Medknow Publications
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Summary:We examined the restorative effect of modified biodegradable chitin conduits in combination with bone marrow mesenchymal stem cell transplantation after right spinal cord hemisection injury. Immunohistochemical staining revealed that biological conduit sleeve bridging reduced glial scar formation and spinal muscular atrophy after spinal cord hemisection. Bone marrow mesenchymal stem cells survived and proliferated after transplantation in vivo, and differentiated into cells double-positive for S100 (Schwann cell marker) and glial fibrillary acidic protein (glial cell marker) at 8 weeks. Retrograde tracing showed that more nerve fibers had grown through the injured spinal cord at 14 weeks after combination therapy than either treatment alone. Our findings indicate that a biological conduit combined with bone marrow mesenchymal stem cell transplantation effectively prevented scar formation and provided a favorable local microenvi- ronment for the proliferation, migration and differentiation of bone marrow mesenchymal stem cells in the spinal cord, thus promoting restoration following spinal cord hemisection injury.
Bibliography:We examined the restorative effect of modified biodegradable chitin conduits in combination with bone marrow mesenchymal stem cell transplantation after right spinal cord hemisection injury. Immunohistochemical staining revealed that biological conduit sleeve bridging reduced glial scar formation and spinal muscular atrophy after spinal cord hemisection. Bone marrow mesenchymal stem cells survived and proliferated after transplantation in vivo, and differentiated into cells double-positive for S100 (Schwann cell marker) and glial fibrillary acidic protein (glial cell marker) at 8 weeks. Retrograde tracing showed that more nerve fibers had grown through the injured spinal cord at 14 weeks after combination therapy than either treatment alone. Our findings indicate that a biological conduit combined with bone marrow mesenchymal stem cell transplantation effectively prevented scar formation and provided a favorable local microenvi- ronment for the proliferation, migration and differentiation of bone marrow mesenchymal stem cells in the spinal cord, thus promoting restoration following spinal cord hemisection injury.
nerve regeneration; spinal cord injury; spinal cord hemisection; biological conduit; bonemarrow mesenchymal stem cells; stem cells; transmission electron microscope; cell transplantation;neurons; nerve fibers; NSFC grants; neural regeneration
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These authors contributed equally to this work.
Author contributions: LYA and FX implemented the experiments. EJW provided experimental data. PXZ, YHK, and NH conceived and designed the study. YHK analyzed experimental data. FX drafted the manuscript. PXZ supervised the manuscript. XFY was responsible for statistical analysis. PXZ and XFY were responsible for the funds. NH provided technical or information support, and revised the study. All authors approved the final version of the manuscript.
ISSN:1673-5374
1876-7958
DOI:10.4103/1673-5374.150715