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Viability of mesenchymal stem cells during electrospinning

Tissue engineering is a technique by which a live tissue can be re-constructed and one of its main goals is to associate cells with biomaterials. Electrospinning is a technique that facilitates the production of nanofibers and is commonly used to develop fibrous scaffolds to be used in tissue engine...

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Autores principales: Zanatta, G., Steffens, D., Braghirolli, D.I., Fernandes, R.A., Netto, C.A., Pranke, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Medicina Tropical 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854255/
https://www.ncbi.nlm.nih.gov/pubmed/22183245
http://dx.doi.org/10.1590/S0100-879X2011007500163
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author Zanatta, G.
Steffens, D.
Braghirolli, D.I.
Fernandes, R.A.
Netto, C.A.
Pranke, P.
author_facet Zanatta, G.
Steffens, D.
Braghirolli, D.I.
Fernandes, R.A.
Netto, C.A.
Pranke, P.
author_sort Zanatta, G.
collection PubMed
description Tissue engineering is a technique by which a live tissue can be re-constructed and one of its main goals is to associate cells with biomaterials. Electrospinning is a technique that facilitates the production of nanofibers and is commonly used to develop fibrous scaffolds to be used in tissue engineering. In the present study, a different approach for cell incorporation into fibrous scaffolds was tested. Mesenchymal stem cells were extracted from the wall of the umbilical cord and mononuclear cells from umbilical cord blood. Cells were re-suspended in a 10% polyvinyl alcohol solution and subjected to electrospinning for 30 min under a voltage of 21 kV. Cell viability was assessed before and after the procedure by exclusion of dead cells using trypan blue staining. Fiber diameter was observed by scanning electron microscopy and the presence of cells within the scaffolds was analyzed by confocal laser scanning microscopy. After electrospinning, the viability of mesenchymal stem cells was reduced from 88 to 19.6% and the viability of mononuclear cells from 99 to 8.38%. The loss of viability was possibly due to the high viscosity of the polymer solution, which reduced the access to nutrients associated with electric and mechanical stress during electrospinning. These results suggest that the incorporation of cells during fiber formation by electrospinning is a viable process that needs more investigation in order to find ways to protect cells from damage.
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spelling pubmed-38542552013-12-16 Viability of mesenchymal stem cells during electrospinning Zanatta, G. Steffens, D. Braghirolli, D.I. Fernandes, R.A. Netto, C.A. Pranke, P. Braz J Med Biol Res Short Communication Tissue engineering is a technique by which a live tissue can be re-constructed and one of its main goals is to associate cells with biomaterials. Electrospinning is a technique that facilitates the production of nanofibers and is commonly used to develop fibrous scaffolds to be used in tissue engineering. In the present study, a different approach for cell incorporation into fibrous scaffolds was tested. Mesenchymal stem cells were extracted from the wall of the umbilical cord and mononuclear cells from umbilical cord blood. Cells were re-suspended in a 10% polyvinyl alcohol solution and subjected to electrospinning for 30 min under a voltage of 21 kV. Cell viability was assessed before and after the procedure by exclusion of dead cells using trypan blue staining. Fiber diameter was observed by scanning electron microscopy and the presence of cells within the scaffolds was analyzed by confocal laser scanning microscopy. After electrospinning, the viability of mesenchymal stem cells was reduced from 88 to 19.6% and the viability of mononuclear cells from 99 to 8.38%. The loss of viability was possibly due to the high viscosity of the polymer solution, which reduced the access to nutrients associated with electric and mechanical stress during electrospinning. These results suggest that the incorporation of cells during fiber formation by electrospinning is a viable process that needs more investigation in order to find ways to protect cells from damage. Sociedade Brasileira de Medicina Tropical 2011-12-23 /pmc/articles/PMC3854255/ /pubmed/22183245 http://dx.doi.org/10.1590/S0100-879X2011007500163 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Zanatta, G.
Steffens, D.
Braghirolli, D.I.
Fernandes, R.A.
Netto, C.A.
Pranke, P.
Viability of mesenchymal stem cells during electrospinning
title Viability of mesenchymal stem cells during electrospinning
title_full Viability of mesenchymal stem cells during electrospinning
title_fullStr Viability of mesenchymal stem cells during electrospinning
title_full_unstemmed Viability of mesenchymal stem cells during electrospinning
title_short Viability of mesenchymal stem cells during electrospinning
title_sort viability of mesenchymal stem cells during electrospinning
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854255/
https://www.ncbi.nlm.nih.gov/pubmed/22183245
http://dx.doi.org/10.1590/S0100-879X2011007500163
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