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Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology

BACKGROUND: Spinal cord injury (SCI) presents a significant challenge for the field of neurotherapeutics. Stem cells have shown promise in replenishing the cells lost to the injury process, but the release of axon growth-inhibitory molecules such as chondroitin sulfate proteoglycans (CSPGs) by activ...

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Autores principales: Jevans, Benjamin, James, Nicholas D., Burnside, Emily, McCann, Conor J., Thapar, Nikhil, Bradbury, Elizabeth J., Burns, Alan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789480/
https://www.ncbi.nlm.nih.gov/pubmed/33407795
http://dx.doi.org/10.1186/s13287-020-02031-9
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author Jevans, Benjamin
James, Nicholas D.
Burnside, Emily
McCann, Conor J.
Thapar, Nikhil
Bradbury, Elizabeth J.
Burns, Alan J.
author_facet Jevans, Benjamin
James, Nicholas D.
Burnside, Emily
McCann, Conor J.
Thapar, Nikhil
Bradbury, Elizabeth J.
Burns, Alan J.
author_sort Jevans, Benjamin
collection PubMed
description BACKGROUND: Spinal cord injury (SCI) presents a significant challenge for the field of neurotherapeutics. Stem cells have shown promise in replenishing the cells lost to the injury process, but the release of axon growth-inhibitory molecules such as chondroitin sulfate proteoglycans (CSPGs) by activated cells within the injury site hinders the integration of transplanted cells. We hypothesised that simultaneous application of enteric neural stem cells (ENSCs) isolated from the gastrointestinal tract, with a lentivirus (LV) containing the enzyme chondroitinase ABC (ChABC), would enhance the regenerative potential of ENSCs after transplantation into the injured spinal cord. METHODS: ENSCs were harvested from the GI tract of p7 rats, expanded in vitro and characterised. Adult rats bearing a contusion injury were randomly assigned to one of four groups: no treatment, LV-ChABC injection only, ENSC transplantation only or ENSC transplantation+LV-ChABC injection. After 16 weeks, rats were sacrificed and the harvested spinal cords examined for evidence of repair. RESULTS: ENSC cultures contained a variety of neuronal subtypes suitable for replenishing cells lost through SCI. Following injury, transplanted ENSC-derived cells survived and ChABC successfully degraded CSPGs. We observed significant reductions in the injured tissue and cavity area, with the greatest improvements seen in the combined treatment group. ENSC-derived cells extended projections across the injury site into both the rostral and caudal host spinal cord, and ENSC transplantation significantly increased the number of cells extending axons across the injury site. Furthermore, the combined treatment resulted in a modest, but significant functional improvement by week 16, and we found no evidence of the spread of transplanted cells to ectopic locations or formation of tumours. CONCLUSIONS: Regenerative effects of a combined treatment with ENSCs and ChABC surpassed either treatment alone, highlighting the importance of further research into combinatorial therapies for SCI. Our work provides evidence that stem cells taken from the adult gastrointestinal tract, an easily accessible source for autologous transplantation, could be strongly considered for the repair of central nervous system disorders.
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spelling pubmed-77894802021-01-07 Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology Jevans, Benjamin James, Nicholas D. Burnside, Emily McCann, Conor J. Thapar, Nikhil Bradbury, Elizabeth J. Burns, Alan J. Stem Cell Res Ther Research BACKGROUND: Spinal cord injury (SCI) presents a significant challenge for the field of neurotherapeutics. Stem cells have shown promise in replenishing the cells lost to the injury process, but the release of axon growth-inhibitory molecules such as chondroitin sulfate proteoglycans (CSPGs) by activated cells within the injury site hinders the integration of transplanted cells. We hypothesised that simultaneous application of enteric neural stem cells (ENSCs) isolated from the gastrointestinal tract, with a lentivirus (LV) containing the enzyme chondroitinase ABC (ChABC), would enhance the regenerative potential of ENSCs after transplantation into the injured spinal cord. METHODS: ENSCs were harvested from the GI tract of p7 rats, expanded in vitro and characterised. Adult rats bearing a contusion injury were randomly assigned to one of four groups: no treatment, LV-ChABC injection only, ENSC transplantation only or ENSC transplantation+LV-ChABC injection. After 16 weeks, rats were sacrificed and the harvested spinal cords examined for evidence of repair. RESULTS: ENSC cultures contained a variety of neuronal subtypes suitable for replenishing cells lost through SCI. Following injury, transplanted ENSC-derived cells survived and ChABC successfully degraded CSPGs. We observed significant reductions in the injured tissue and cavity area, with the greatest improvements seen in the combined treatment group. ENSC-derived cells extended projections across the injury site into both the rostral and caudal host spinal cord, and ENSC transplantation significantly increased the number of cells extending axons across the injury site. Furthermore, the combined treatment resulted in a modest, but significant functional improvement by week 16, and we found no evidence of the spread of transplanted cells to ectopic locations or formation of tumours. CONCLUSIONS: Regenerative effects of a combined treatment with ENSCs and ChABC surpassed either treatment alone, highlighting the importance of further research into combinatorial therapies for SCI. Our work provides evidence that stem cells taken from the adult gastrointestinal tract, an easily accessible source for autologous transplantation, could be strongly considered for the repair of central nervous system disorders. BioMed Central 2021-01-06 /pmc/articles/PMC7789480/ /pubmed/33407795 http://dx.doi.org/10.1186/s13287-020-02031-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jevans, Benjamin
James, Nicholas D.
Burnside, Emily
McCann, Conor J.
Thapar, Nikhil
Bradbury, Elizabeth J.
Burns, Alan J.
Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology
title Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology
title_full Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology
title_fullStr Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology
title_full_unstemmed Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology
title_short Combined treatment with enteric neural stem cells and chondroitinase ABC reduces spinal cord lesion pathology
title_sort combined treatment with enteric neural stem cells and chondroitinase abc reduces spinal cord lesion pathology
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789480/
https://www.ncbi.nlm.nih.gov/pubmed/33407795
http://dx.doi.org/10.1186/s13287-020-02031-9
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