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Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell Transplantation Therapy in Spinal Cord Injury Mice
Bone marrow stromal cell (BMSC) transplantation has been reported as treatments that promote functional recovery after spinal cord injury (SCI) in humans and animals. Polyethylene glycol (PEG) has been also reported as treatments that promote functional recovery after spinal cord injury (SCI) in hum...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013369/ https://www.ncbi.nlm.nih.gov/pubmed/24270802 http://dx.doi.org/10.1292/jvms.13-0167 |
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author | ODA, Yasutaka TANI, Kenji ISOZAKI, Atsunobu HARAGUCHI, Tomoya ITAMOTO, Kazuhito NAKAZAWA, Hiroshi TAURA, Yasuho |
author_facet | ODA, Yasutaka TANI, Kenji ISOZAKI, Atsunobu HARAGUCHI, Tomoya ITAMOTO, Kazuhito NAKAZAWA, Hiroshi TAURA, Yasuho |
author_sort | ODA, Yasutaka |
collection | PubMed |
description | Bone marrow stromal cell (BMSC) transplantation has been reported as treatments that promote functional recovery after spinal cord injury (SCI) in humans and animals. Polyethylene glycol (PEG) has been also reported as treatments that promote functional recovery after spinal cord injury (SCI) in humans and animals. Therefore, administration of PEG combined with BMSC transplantation may improve outcomes compared with BMSC transplantation only in SCI model mice. SCI mice were divided into a control-group, BMSC-group, PEG-group and BMSC+PEG-group. BMSC transplantation and PEG administration were performed immediately after surgery. Compared to the control-group, PEG- and BMSC+PEG-groups showed significant locomotor functional recovery 4 weeks after therapy. We observed no significant differences among the groups. In the BMSC- and BMSC+PEG-groups, immunohistochemistry showed that many neuronal cells aggressively migrated toward the glial scar from the region rostral of the lesion site. In the control- and PEG-groups, the boundary of the injured regions was covered with astrocytes, and a few neuronal cells were migrated toward the glial scar. We conclude that combined BMSC transplantation with PEG treatment showed no synergistic effects on locomotor functional recovery or beneficial cellular events. Further studies may improve the effect of the treatment, including modification of the timing of BMSC transplantation. |
format | Online Article Text |
id | pubmed-4013369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40133692014-05-13 Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell Transplantation Therapy in Spinal Cord Injury Mice ODA, Yasutaka TANI, Kenji ISOZAKI, Atsunobu HARAGUCHI, Tomoya ITAMOTO, Kazuhito NAKAZAWA, Hiroshi TAURA, Yasuho J Vet Med Sci Laboratory Animal Science Bone marrow stromal cell (BMSC) transplantation has been reported as treatments that promote functional recovery after spinal cord injury (SCI) in humans and animals. Polyethylene glycol (PEG) has been also reported as treatments that promote functional recovery after spinal cord injury (SCI) in humans and animals. Therefore, administration of PEG combined with BMSC transplantation may improve outcomes compared with BMSC transplantation only in SCI model mice. SCI mice were divided into a control-group, BMSC-group, PEG-group and BMSC+PEG-group. BMSC transplantation and PEG administration were performed immediately after surgery. Compared to the control-group, PEG- and BMSC+PEG-groups showed significant locomotor functional recovery 4 weeks after therapy. We observed no significant differences among the groups. In the BMSC- and BMSC+PEG-groups, immunohistochemistry showed that many neuronal cells aggressively migrated toward the glial scar from the region rostral of the lesion site. In the control- and PEG-groups, the boundary of the injured regions was covered with astrocytes, and a few neuronal cells were migrated toward the glial scar. We conclude that combined BMSC transplantation with PEG treatment showed no synergistic effects on locomotor functional recovery or beneficial cellular events. Further studies may improve the effect of the treatment, including modification of the timing of BMSC transplantation. The Japanese Society of Veterinary Science 2013-11-22 2014-03 /pmc/articles/PMC4013369/ /pubmed/24270802 http://dx.doi.org/10.1292/jvms.13-0167 Text en ©2014 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Laboratory Animal Science ODA, Yasutaka TANI, Kenji ISOZAKI, Atsunobu HARAGUCHI, Tomoya ITAMOTO, Kazuhito NAKAZAWA, Hiroshi TAURA, Yasuho Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell Transplantation Therapy in Spinal Cord Injury Mice |
title | Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell
Transplantation Therapy in Spinal Cord Injury Mice |
title_full | Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell
Transplantation Therapy in Spinal Cord Injury Mice |
title_fullStr | Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell
Transplantation Therapy in Spinal Cord Injury Mice |
title_full_unstemmed | Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell
Transplantation Therapy in Spinal Cord Injury Mice |
title_short | Effects of Polyethylene Glycol Administration and Bone Marrow Stromal Cell
Transplantation Therapy in Spinal Cord Injury Mice |
title_sort | effects of polyethylene glycol administration and bone marrow stromal cell
transplantation therapy in spinal cord injury mice |
topic | Laboratory Animal Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013369/ https://www.ncbi.nlm.nih.gov/pubmed/24270802 http://dx.doi.org/10.1292/jvms.13-0167 |
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