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Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats

BACKGROUND: Proof of the efficacy and safety of a xenogeneic mesenchymal stem cell (MSCs) transplant for spinal cord injury (SCI) may theoretically widen the spectrum of possible grafts for neuroregeneration. METHODS: Twenty rats were submitted to complete spinal cord transection. Ovine bone marrow...

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Autores principales: Sabino, Luzzi, Maria, Crovace Alberto, Luca, Lacitignola, Valerio, Valentini, Edda, Francioso, Giacomo, Rossi, Gloria, Invernici, Juan, Galzio Renato, Antonio, Crovace
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806420/
https://www.ncbi.nlm.nih.gov/pubmed/29497572
http://dx.doi.org/10.4103/sni.sni_369_17
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author Sabino, Luzzi
Maria, Crovace Alberto
Luca, Lacitignola
Valerio, Valentini
Edda, Francioso
Giacomo, Rossi
Gloria, Invernici
Juan, Galzio Renato
Antonio, Crovace
author_facet Sabino, Luzzi
Maria, Crovace Alberto
Luca, Lacitignola
Valerio, Valentini
Edda, Francioso
Giacomo, Rossi
Gloria, Invernici
Juan, Galzio Renato
Antonio, Crovace
author_sort Sabino, Luzzi
collection PubMed
description BACKGROUND: Proof of the efficacy and safety of a xenogeneic mesenchymal stem cell (MSCs) transplant for spinal cord injury (SCI) may theoretically widen the spectrum of possible grafts for neuroregeneration. METHODS: Twenty rats were submitted to complete spinal cord transection. Ovine bone marrow MSCs, retrovirally transfected with red fluorescent protein and not previously induced for neuroglial differentiation, were applied in 10 study rats (MSCG). Fibrin glue was injected in 10 control rats (FGG). All rats were evaluated on a weekly basis and scored using the Basso–Beattie–Bresnahan (BBB) locomotor scale for 10 weeks, when the collected data were statistically analyzed. The spinal cords were then harvested and analyzed with light microscopy, immunohistochemistry, and immunofluorescence. RESULTS: Ovine MSCs culture showed positivity for Nestin. MSCG had a significant and durable recovery of motor functions (P <.001). Red fluorescence was found at the injury sites in MSCG. Positivity for Nestin, tubulin βIII, NG2 glia, neuron-specific enolase, vimentin, and 200 kD neurofilament were also found at the same sites. CONCLUSIONS: Xenogeneic ovine bone marrow MSCs proved capable of engrafting into the injured rat spinal cord. Transdifferentiation into a neuroglial phenotype was able to support partial functional recovery.
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spelling pubmed-58064202018-03-01 Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats Sabino, Luzzi Maria, Crovace Alberto Luca, Lacitignola Valerio, Valentini Edda, Francioso Giacomo, Rossi Gloria, Invernici Juan, Galzio Renato Antonio, Crovace Surg Neurol Int Head and Spinal Cord Transplantation: Original Article BACKGROUND: Proof of the efficacy and safety of a xenogeneic mesenchymal stem cell (MSCs) transplant for spinal cord injury (SCI) may theoretically widen the spectrum of possible grafts for neuroregeneration. METHODS: Twenty rats were submitted to complete spinal cord transection. Ovine bone marrow MSCs, retrovirally transfected with red fluorescent protein and not previously induced for neuroglial differentiation, were applied in 10 study rats (MSCG). Fibrin glue was injected in 10 control rats (FGG). All rats were evaluated on a weekly basis and scored using the Basso–Beattie–Bresnahan (BBB) locomotor scale for 10 weeks, when the collected data were statistically analyzed. The spinal cords were then harvested and analyzed with light microscopy, immunohistochemistry, and immunofluorescence. RESULTS: Ovine MSCs culture showed positivity for Nestin. MSCG had a significant and durable recovery of motor functions (P <.001). Red fluorescence was found at the injury sites in MSCG. Positivity for Nestin, tubulin βIII, NG2 glia, neuron-specific enolase, vimentin, and 200 kD neurofilament were also found at the same sites. CONCLUSIONS: Xenogeneic ovine bone marrow MSCs proved capable of engrafting into the injured rat spinal cord. Transdifferentiation into a neuroglial phenotype was able to support partial functional recovery. Medknow Publications & Media Pvt Ltd 2018-01-25 /pmc/articles/PMC5806420/ /pubmed/29497572 http://dx.doi.org/10.4103/sni.sni_369_17 Text en Copyright: © 2018 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Head and Spinal Cord Transplantation: Original Article
Sabino, Luzzi
Maria, Crovace Alberto
Luca, Lacitignola
Valerio, Valentini
Edda, Francioso
Giacomo, Rossi
Gloria, Invernici
Juan, Galzio Renato
Antonio, Crovace
Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats
title Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats
title_full Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats
title_fullStr Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats
title_full_unstemmed Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats
title_short Engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats
title_sort engraftment, neuroglial transdifferentiation and behavioral recovery after complete spinal cord transection in rats
topic Head and Spinal Cord Transplantation: Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806420/
https://www.ncbi.nlm.nih.gov/pubmed/29497572
http://dx.doi.org/10.4103/sni.sni_369_17
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