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Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats

Spinal cord injuries are still a serious problem for regenerative medicine. Previous research has demonstrated that activated microglia accumulate in spinal lesions, influencing the injured tissues in various ways. Therefore, transplantation of activated microglia may have a beneficial role in the r...

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Autores principales: Marcol, Wiesław, Ślusarczyk, Wojciech, Larysz-Brysz, Magdalena, Łabuzek, Krzysztof, Kapustka, Bartosz, Staszkiewicz, Rafał, Rosicka, Paulina, Kalita, Katarzyna, Węglarz, Władysław, Lewin-Kowalik, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704303/
https://www.ncbi.nlm.nih.gov/pubmed/29201191
http://dx.doi.org/10.3892/etm.2017.5130
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author Marcol, Wiesław
Ślusarczyk, Wojciech
Larysz-Brysz, Magdalena
Łabuzek, Krzysztof
Kapustka, Bartosz
Staszkiewicz, Rafał
Rosicka, Paulina
Kalita, Katarzyna
Węglarz, Władysław
Lewin-Kowalik, Joanna
author_facet Marcol, Wiesław
Ślusarczyk, Wojciech
Larysz-Brysz, Magdalena
Łabuzek, Krzysztof
Kapustka, Bartosz
Staszkiewicz, Rafał
Rosicka, Paulina
Kalita, Katarzyna
Węglarz, Władysław
Lewin-Kowalik, Joanna
author_sort Marcol, Wiesław
collection PubMed
description Spinal cord injuries are still a serious problem for regenerative medicine. Previous research has demonstrated that activated microglia accumulate in spinal lesions, influencing the injured tissues in various ways. Therefore, transplantation of activated microglia may have a beneficial role in the regeneration of the nervous system. The present study examined the influence of transplanted activated microglial cells in adult rats with injured spinal cords. Rats were randomly divided into an experimental (M) and control (C) group, and were subjected to non-laminectomy focal injury of spinal cord white matter by means of a high-pressured air stream. In group M, activated cultured microglial cells were injected twice into the site of injury. Functional outcome and morphological features of regeneration were analyzed during a 12-week follow-up. The lesions were characterized by means of magnetic resonance imaging (MRI). Neurons in the brain stem and motor cortex were labeled with FluoroGold (FG). A total of 12 weeks after surgery, spinal cords and brains were collected and subjected to histopathological and immunohistochemical examinations. Lesion sizes in the spinal cord were measured and the number of FG-positive neurons was counted. Rats in group M demonstrated significant improvement of locomotor performance when compared with group C (P<0.05). MRI analysis demonstrated moderate improvement in water diffusion along the spinal cord in the group M following microglia treatment, as compared with group C. The water diffusion perpendicular to the spinal cord in group M was closer to the reference values for a healthy spinal cord than it was in group C. The sizes of lesions were also significantly smaller in group M than in the group C (P<0.05). The number of brain stem and motor cortex FG-positive neurons in group M was significantly higher than in group C. The present study demonstrated that delivery of activated microglia directly into the injured spinal cord gives some positive effects for the regeneration of the white matter.
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spelling pubmed-57043032017-11-30 Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats Marcol, Wiesław Ślusarczyk, Wojciech Larysz-Brysz, Magdalena Łabuzek, Krzysztof Kapustka, Bartosz Staszkiewicz, Rafał Rosicka, Paulina Kalita, Katarzyna Węglarz, Władysław Lewin-Kowalik, Joanna Exp Ther Med Articles Spinal cord injuries are still a serious problem for regenerative medicine. Previous research has demonstrated that activated microglia accumulate in spinal lesions, influencing the injured tissues in various ways. Therefore, transplantation of activated microglia may have a beneficial role in the regeneration of the nervous system. The present study examined the influence of transplanted activated microglial cells in adult rats with injured spinal cords. Rats were randomly divided into an experimental (M) and control (C) group, and were subjected to non-laminectomy focal injury of spinal cord white matter by means of a high-pressured air stream. In group M, activated cultured microglial cells were injected twice into the site of injury. Functional outcome and morphological features of regeneration were analyzed during a 12-week follow-up. The lesions were characterized by means of magnetic resonance imaging (MRI). Neurons in the brain stem and motor cortex were labeled with FluoroGold (FG). A total of 12 weeks after surgery, spinal cords and brains were collected and subjected to histopathological and immunohistochemical examinations. Lesion sizes in the spinal cord were measured and the number of FG-positive neurons was counted. Rats in group M demonstrated significant improvement of locomotor performance when compared with group C (P<0.05). MRI analysis demonstrated moderate improvement in water diffusion along the spinal cord in the group M following microglia treatment, as compared with group C. The water diffusion perpendicular to the spinal cord in group M was closer to the reference values for a healthy spinal cord than it was in group C. The sizes of lesions were also significantly smaller in group M than in the group C (P<0.05). The number of brain stem and motor cortex FG-positive neurons in group M was significantly higher than in group C. The present study demonstrated that delivery of activated microglia directly into the injured spinal cord gives some positive effects for the regeneration of the white matter. D.A. Spandidos 2017-11 2017-09-19 /pmc/articles/PMC5704303/ /pubmed/29201191 http://dx.doi.org/10.3892/etm.2017.5130 Text en Copyright: © Marcol et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Marcol, Wiesław
Ślusarczyk, Wojciech
Larysz-Brysz, Magdalena
Łabuzek, Krzysztof
Kapustka, Bartosz
Staszkiewicz, Rafał
Rosicka, Paulina
Kalita, Katarzyna
Węglarz, Władysław
Lewin-Kowalik, Joanna
Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats
title Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats
title_full Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats
title_fullStr Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats
title_full_unstemmed Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats
title_short Extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats
title_sort extended magnetic resonance imaging studies on the effect of classically activated microglia transplantation on white matter regeneration following spinal cord focal injury in adult rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704303/
https://www.ncbi.nlm.nih.gov/pubmed/29201191
http://dx.doi.org/10.3892/etm.2017.5130
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