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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 : 000A10

Cell 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 :

RBID : PMC:4819730

Abstract

Background

The aim of this study is to verify the feasibility of using silk fibroin (SF) as a potential membrane for guided bone regeneration (GBR).

Methods

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.

Results

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 (P < 0.05); however, at respective time points, cell viability was not significantly different between the two groups (P > 0.05). In contrast, cell proliferation was significantly higher in the SF membrane group than in the control group at 7 days (P < 0.05).

Conclusions

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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PMC:4819730

Le document en format XML

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<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>
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<p>These results suggest that silk fibroin is a biocompatible material that could be used as a suitable alternative barrier membrane for GBR.</p>
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