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Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats

Traumatic spinal cord injury (SCI) is a devastating condition without an effective therapy. Cellular therapies are among the promising treatment strategies. Adult stem cells, such as mesenchymal stem cells, are often used clinical research for their immunomodulatory and regenerative potential. This...

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Autores principales: Vialle, Emiliano Neves, Fracaro, Letícia, Barchiki, Fabiane, Dominguez, Alejandro Correa, Arruda, André de Oliveira, Olandoski, Marcia, Brofman, Paulo Roberto Slud, Kuniyoshi Rebelatto, Carmen Lúcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216621/
https://www.ncbi.nlm.nih.gov/pubmed/37239065
http://dx.doi.org/10.3390/biomedicines11051394
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author Vialle, Emiliano Neves
Fracaro, Letícia
Barchiki, Fabiane
Dominguez, Alejandro Correa
Arruda, André de Oliveira
Olandoski, Marcia
Brofman, Paulo Roberto Slud
Kuniyoshi Rebelatto, Carmen Lúcia
author_facet Vialle, Emiliano Neves
Fracaro, Letícia
Barchiki, Fabiane
Dominguez, Alejandro Correa
Arruda, André de Oliveira
Olandoski, Marcia
Brofman, Paulo Roberto Slud
Kuniyoshi Rebelatto, Carmen Lúcia
author_sort Vialle, Emiliano Neves
collection PubMed
description Traumatic spinal cord injury (SCI) is a devastating condition without an effective therapy. Cellular therapies are among the promising treatment strategies. Adult stem cells, such as mesenchymal stem cells, are often used clinical research for their immunomodulatory and regenerative potential. This study aimed to evaluate the effect of human adipose tissue-derived stem cells (ADSC) infusion through the cauda equina in rats with SCI. The human ADSC from bariatric surgery was isolated, expanded, and characterized. Wistar rats were subjected to blunt SCI and were divided into four groups. Two experimental groups (EG): EG1 received one ADSC infusion after SCI, and EG2 received two infusions, the first one after SCI and the second infusion seven days after the injury. Control groups (CG1 and CG2) received infusion with a culture medium. In vivo, cell tracking was performed 48 h and seven days after ADSC infusion. The animals were followed up for 40 days after SCI, and immunohistochemical quantification of myelin, neurons, and astrocytes was performed. Cellular tracking showed cell migration towards the injury site. ADSC infusion significantly reduced neuronal loss, although it did not prevent the myelin loss or enhance the area occupied by astrocytes compared to the control group. The results were similar when comparing one or two cell infusions. The injection of ADSC distal to the injured area was shown to be a safe and effective method for cellular administration in spinal cord injury.
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spelling pubmed-102166212023-05-27 Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats Vialle, Emiliano Neves Fracaro, Letícia Barchiki, Fabiane Dominguez, Alejandro Correa Arruda, André de Oliveira Olandoski, Marcia Brofman, Paulo Roberto Slud Kuniyoshi Rebelatto, Carmen Lúcia Biomedicines Article Traumatic spinal cord injury (SCI) is a devastating condition without an effective therapy. Cellular therapies are among the promising treatment strategies. Adult stem cells, such as mesenchymal stem cells, are often used clinical research for their immunomodulatory and regenerative potential. This study aimed to evaluate the effect of human adipose tissue-derived stem cells (ADSC) infusion through the cauda equina in rats with SCI. The human ADSC from bariatric surgery was isolated, expanded, and characterized. Wistar rats were subjected to blunt SCI and were divided into four groups. Two experimental groups (EG): EG1 received one ADSC infusion after SCI, and EG2 received two infusions, the first one after SCI and the second infusion seven days after the injury. Control groups (CG1 and CG2) received infusion with a culture medium. In vivo, cell tracking was performed 48 h and seven days after ADSC infusion. The animals were followed up for 40 days after SCI, and immunohistochemical quantification of myelin, neurons, and astrocytes was performed. Cellular tracking showed cell migration towards the injury site. ADSC infusion significantly reduced neuronal loss, although it did not prevent the myelin loss or enhance the area occupied by astrocytes compared to the control group. The results were similar when comparing one or two cell infusions. The injection of ADSC distal to the injured area was shown to be a safe and effective method for cellular administration in spinal cord injury. MDPI 2023-05-08 /pmc/articles/PMC10216621/ /pubmed/37239065 http://dx.doi.org/10.3390/biomedicines11051394 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vialle, Emiliano Neves
Fracaro, Letícia
Barchiki, Fabiane
Dominguez, Alejandro Correa
Arruda, André de Oliveira
Olandoski, Marcia
Brofman, Paulo Roberto Slud
Kuniyoshi Rebelatto, Carmen Lúcia
Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats
title Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats
title_full Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats
title_fullStr Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats
title_full_unstemmed Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats
title_short Human Adipose-Derived Stem Cells Reduce Cellular Damage after Experimental Spinal Cord Injury in Rats
title_sort human adipose-derived stem cells reduce cellular damage after experimental spinal cord injury in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216621/
https://www.ncbi.nlm.nih.gov/pubmed/37239065
http://dx.doi.org/10.3390/biomedicines11051394
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