Cell attachment and proliferation of osteoblast-like MG63 cells on silk fibroin membrane for guided bone regeneration
Identifieur interne : 000A09 ( Main/Curation ); précédent : 000A08; suivant : 000A10Cell attachment and proliferation of osteoblast-like MG63 cells on silk fibroin membrane for guided bone regeneration
Auteurs : Chae-Kyung Yoo [Corée du Sud] ; Jae-Yun Jeon [Corée du Sud] ; You-Jin Kim [Corée du Sud] ; Seong-Gon Kim [Corée du Sud] ; Kyung-Gyun Hwang [Corée du Sud]Source :
- Maxillofacial Plastic and Reconstructive Surgery [ 2288-8101 ] ; 2016.
Abstract
The aim of this study is to verify the feasibility of using silk fibroin (SF) as a potential membrane for guided bone regeneration (GBR).
Various cellular responses (i.e., cell attachment, viability, and proliferation) of osteoblast-like MG63 cells cultured on an SF membrane were quantified. After culturing on an SF membrane for 1, 5, and 7 days, the attachment and surface morphology of MG63 cells were examined by optical and scanning electron microscopy (SEM), cell viability was determined using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and cell proliferation was quantified using 4′,6-diamidino-2-phenylindole (DAPI) fluorescence staining.
Optical microscopy revealed that MG63 cells cultured on the SF membrane proliferated over the 7-day observation period. The viability of cells cultured on SF membranes (SF group) and on control surfaces (control group) increased over time (
These results suggest that silk fibroin is a biocompatible material that could be used as a suitable alternative barrier membrane for GBR.
Url:
DOI: 10.1186/s40902-016-0062-4
PubMed: 27073799
PubMed Central: 4819730
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<series><title level="j">Maxillofacial Plastic and Reconstructive Surgery</title>
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p>The aim of this study is to verify the feasibility of using silk fibroin (SF) as a potential membrane for guided bone regeneration (GBR).</p>
</sec>
<sec><title>Methods</title>
<p>Various cellular responses (i.e., cell attachment, viability, and proliferation) of osteoblast-like MG63 cells cultured on an SF membrane were quantified. After culturing on an SF membrane for 1, 5, and 7 days, the attachment and surface morphology of MG63 cells were examined by optical and scanning electron microscopy (SEM), cell viability was determined using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and cell proliferation was quantified using 4′,6-diamidino-2-phenylindole (DAPI) fluorescence staining.</p>
</sec>
<sec><title>Results</title>
<p>Optical microscopy revealed that MG63 cells cultured on the SF membrane proliferated over the 7-day observation period. The viability of cells cultured on SF membranes (SF group) and on control surfaces (control group) increased over time (<italic>P</italic>
< 0.05); however, at respective time points, cell viability was not significantly different between the two groups (<italic>P</italic>
> 0.05). In contrast, cell proliferation was significantly higher in the SF membrane group than in the control group at 7 days (<italic>P</italic>
< 0.05).</p>
</sec>
<sec><title>Conclusions</title>
<p>These results suggest that silk fibroin is a biocompatible material that could be used as a suitable alternative barrier membrane for GBR.</p>
</sec>
</div>
</front>
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