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Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro

The use of tissue engineering technology in the repair of spinal cord injury (SCI) is a topic of current interest. The success of the repair of the SCI is directly affected by the selection of suitable seed cells and scaffold materials with an acceptable biocompatibility. In this study, adipose tiss...

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Autores principales: JI, WENCHEN, ZHANG, YUELIN, HU, SHOUYE, ZHANG, YONGTAO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786727/
https://www.ncbi.nlm.nih.gov/pubmed/24137218
http://dx.doi.org/10.3892/etm.2013.1185
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author JI, WENCHEN
ZHANG, YUELIN
HU, SHOUYE
ZHANG, YONGTAO
author_facet JI, WENCHEN
ZHANG, YUELIN
HU, SHOUYE
ZHANG, YONGTAO
author_sort JI, WENCHEN
collection PubMed
description The use of tissue engineering technology in the repair of spinal cord injury (SCI) is a topic of current interest. The success of the repair of the SCI is directly affected by the selection of suitable seed cells and scaffold materials with an acceptable biocompatibility. In this study, adipose tissue-derived stem cells (ADSCs) were incorporated into a silk fibroin-chitosan scaffold (SFCS), which was constructed using a freeze-drying method, in order to assess the biocompatibility of the ADSCs and the SFCS and to provide a foundation for the use of tissue engineering technology in the repair of SCI. Following the seeding of the cells onto the scaffold, the adhesion characteristics of the ADSCs and the SFCS were assessed. A significant difference was observed between the experimental group (a composite of the ADSCs with the SFCS) and the control group (ADSCs without the scaffold) following a culture period of 6 h (P<0.05). The differences in the results at the following time-points were statistically insignificant (P>0.05). The use of an MTT assay to assess the proliferation of the cells on the scaffold revealed that there were significant differences between the experimental and control groups following culture periods of 2 and 4 days (P<0.05). However, the results at the subsequent time-points were not statistically significantly different (P>0.05). Scanning electron microscopy (SEM), using hematoxylin and eosin (H&E) staining, was used to observe the cellular morphology following seeding, and this revealed that the cells displayed the desired morphology. The results indicate that ADSCs have a good biocompatibility with a SFCS and thus provide a foundation for further studies using tissue engineering methods for the repair of SCI.
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spelling pubmed-37867272013-10-17 Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro JI, WENCHEN ZHANG, YUELIN HU, SHOUYE ZHANG, YONGTAO Exp Ther Med Articles The use of tissue engineering technology in the repair of spinal cord injury (SCI) is a topic of current interest. The success of the repair of the SCI is directly affected by the selection of suitable seed cells and scaffold materials with an acceptable biocompatibility. In this study, adipose tissue-derived stem cells (ADSCs) were incorporated into a silk fibroin-chitosan scaffold (SFCS), which was constructed using a freeze-drying method, in order to assess the biocompatibility of the ADSCs and the SFCS and to provide a foundation for the use of tissue engineering technology in the repair of SCI. Following the seeding of the cells onto the scaffold, the adhesion characteristics of the ADSCs and the SFCS were assessed. A significant difference was observed between the experimental group (a composite of the ADSCs with the SFCS) and the control group (ADSCs without the scaffold) following a culture period of 6 h (P<0.05). The differences in the results at the following time-points were statistically insignificant (P>0.05). The use of an MTT assay to assess the proliferation of the cells on the scaffold revealed that there were significant differences between the experimental and control groups following culture periods of 2 and 4 days (P<0.05). However, the results at the subsequent time-points were not statistically significantly different (P>0.05). Scanning electron microscopy (SEM), using hematoxylin and eosin (H&E) staining, was used to observe the cellular morphology following seeding, and this revealed that the cells displayed the desired morphology. The results indicate that ADSCs have a good biocompatibility with a SFCS and thus provide a foundation for further studies using tissue engineering methods for the repair of SCI. D.A. Spandidos 2013-08 2013-06-26 /pmc/articles/PMC3786727/ /pubmed/24137218 http://dx.doi.org/10.3892/etm.2013.1185 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
JI, WENCHEN
ZHANG, YUELIN
HU, SHOUYE
ZHANG, YONGTAO
Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro
title Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro
title_full Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro
title_fullStr Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro
title_full_unstemmed Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro
title_short Biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro
title_sort biocompatibility study of a silk fibroin-chitosan scaffold with adipose tissue-derived stem cells in vitro
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786727/
https://www.ncbi.nlm.nih.gov/pubmed/24137218
http://dx.doi.org/10.3892/etm.2013.1185
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