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Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats

Cell therapy is a promising strategy to pursue the unmet need for treatment of spinal cord injury (SCI). Although several studies have shown that adult mesenchymal cells contribute to improve the outcomes of SCI, a descripton of the pro-regenerative events triggered by these cells is still lacking....

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Autores principales: Menezes, Karla, Nascimento, Marcos Assis, Gonçalves, Juliana Pena, Cruz, Aline Silva, Lopes, Daiana Vieira, Curzio, Bianca, Bonamino, Martin, de Menezes, João Ricardo Lacerda, Borojevic, Radovan, Rossi, Maria Isabel Doria, Coelho-Sampaio, Tatiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022508/
https://www.ncbi.nlm.nih.gov/pubmed/24830794
http://dx.doi.org/10.1371/journal.pone.0096020
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author Menezes, Karla
Nascimento, Marcos Assis
Gonçalves, Juliana Pena
Cruz, Aline Silva
Lopes, Daiana Vieira
Curzio, Bianca
Bonamino, Martin
de Menezes, João Ricardo Lacerda
Borojevic, Radovan
Rossi, Maria Isabel Doria
Coelho-Sampaio, Tatiana
author_facet Menezes, Karla
Nascimento, Marcos Assis
Gonçalves, Juliana Pena
Cruz, Aline Silva
Lopes, Daiana Vieira
Curzio, Bianca
Bonamino, Martin
de Menezes, João Ricardo Lacerda
Borojevic, Radovan
Rossi, Maria Isabel Doria
Coelho-Sampaio, Tatiana
author_sort Menezes, Karla
collection PubMed
description Cell therapy is a promising strategy to pursue the unmet need for treatment of spinal cord injury (SCI). Although several studies have shown that adult mesenchymal cells contribute to improve the outcomes of SCI, a descripton of the pro-regenerative events triggered by these cells is still lacking. Here we investigated the regenerative properties of human adipose tissue derived stromal cells (hADSCs) in a rat model of spinal cord compression. Cells were delivered directly into the spinal parenchyma immediately after injury. Human ADSCs promoted functional recovery, tissue preservation, and axonal regeneration. Analysis of the cord tissue showed an abundant deposition of laminin of human origin at the lesion site and spinal midline; the appearance of cell clusters composed of neural precursors in the areas of laminin deposition, and the appearance of blood vessels with separated basement membranes along the spinal axis. These effects were also observed after injection of hADSCs into non-injured spinal cord. Considering that laminin is a well-known inducer of axonal growth, as well a component of the extracellular matrix associated to neural progenitors, we propose that it can be the paracrine factor mediating the pro-regenerative effects of hADSCs in spinal cord injury.
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spelling pubmed-40225082014-05-21 Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats Menezes, Karla Nascimento, Marcos Assis Gonçalves, Juliana Pena Cruz, Aline Silva Lopes, Daiana Vieira Curzio, Bianca Bonamino, Martin de Menezes, João Ricardo Lacerda Borojevic, Radovan Rossi, Maria Isabel Doria Coelho-Sampaio, Tatiana PLoS One Research Article Cell therapy is a promising strategy to pursue the unmet need for treatment of spinal cord injury (SCI). Although several studies have shown that adult mesenchymal cells contribute to improve the outcomes of SCI, a descripton of the pro-regenerative events triggered by these cells is still lacking. Here we investigated the regenerative properties of human adipose tissue derived stromal cells (hADSCs) in a rat model of spinal cord compression. Cells were delivered directly into the spinal parenchyma immediately after injury. Human ADSCs promoted functional recovery, tissue preservation, and axonal regeneration. Analysis of the cord tissue showed an abundant deposition of laminin of human origin at the lesion site and spinal midline; the appearance of cell clusters composed of neural precursors in the areas of laminin deposition, and the appearance of blood vessels with separated basement membranes along the spinal axis. These effects were also observed after injection of hADSCs into non-injured spinal cord. Considering that laminin is a well-known inducer of axonal growth, as well a component of the extracellular matrix associated to neural progenitors, we propose that it can be the paracrine factor mediating the pro-regenerative effects of hADSCs in spinal cord injury. Public Library of Science 2014-05-15 /pmc/articles/PMC4022508/ /pubmed/24830794 http://dx.doi.org/10.1371/journal.pone.0096020 Text en © 2014 Menezes et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Menezes, Karla
Nascimento, Marcos Assis
Gonçalves, Juliana Pena
Cruz, Aline Silva
Lopes, Daiana Vieira
Curzio, Bianca
Bonamino, Martin
de Menezes, João Ricardo Lacerda
Borojevic, Radovan
Rossi, Maria Isabel Doria
Coelho-Sampaio, Tatiana
Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats
title Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats
title_full Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats
title_fullStr Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats
title_full_unstemmed Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats
title_short Human Mesenchymal Cells from Adipose Tissue Deposit Laminin and Promote Regeneration of Injured Spinal Cord in Rats
title_sort human mesenchymal cells from adipose tissue deposit laminin and promote regeneration of injured spinal cord in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022508/
https://www.ncbi.nlm.nih.gov/pubmed/24830794
http://dx.doi.org/10.1371/journal.pone.0096020
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