Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/142380
Title: Osteogenic differentiation of mesenchymal stem cells with silica-coated gold nanoparticles for bone tissue engineering
Authors: Gandhimathi, Chinnasamy
Quek, Ying Jie
Ezhilarasu, Hariharan
Ramakrishna, Seeram
Bay, Boon-Huat
Srinivasan, Dinesh Kumar
Keywords: Science::Biological sciences
Issue Date: 2019
Source: Gandhimathi, C., Quek, Y. J., Ezhilarasu, H., Ramakrishna, S., Bay, B.-H., & Srinivasan, D. K.. (2019). Osteogenic differentiation of Mesenchymal stem cells with silica-coated gold nanoparticles for bone tissue engineering. International Journal of Molecular Sciences, 20(20), 5135-. doi:10.3390/ijms20205135
Journal: International Journal of Molecular Sciences
Abstract: Multifunctional nanofibrous scaffolds for effective bone tissue engineering (BTE) application must incorporate factors to promote neovascularization and tissue regeneration. In this study, silica-coated gold nanoparticles Au(SiO2) were tested for their ability to promote differentiation of human mesenchymal stem cells (hMSCs) into osteoblasts. Biocompatible poly-ε-caprolactone (PCL), PCL/silk fibroin (SF) and PCL/SF/Au(SiO2) loaded nanofibrous scaffolds were first fabricated by an electrospinning method. Electrospun nanofibrous scaffolds were characterized for fiber architecture, porosity, pore size distribution, fiber wettability and the relevant mechanical properties using field emission scanning electron microscopy (FESEM), porosimetry, determination of water contact angle, measurements by a surface analyzer and tabletop tensile-tester measurements. FESEM images of the scaffolds revealed beadless, porous, uniform fibers with diameters in the range of 164 ± 18.65 nm to 215 ± 32.12 nm and porosity of around 88-92% and pore size distribution around 1.45-2.35 µm. Following hMSCs were cultured on the composite scaffolds. Cell-scaffold interaction, morphology and proliferation of were analyzed by FESEM analysis, MTS (3-(4,5-dimethyl thiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium inner salt) and CMFDA (5-choromethyl fluorescein acetate) dye assays. Osteogenic differentiation of MSCs into osteogenic cells were determined by alkaline phosphatase (ALP) activity, mineralization by alizarin red S (ARS) staining and osteocalcin expression by immunofluorescence staining. The results revealed that the addition of SF and Au(SiO2) to PCL scaffolds enhanced the mechanical strength, interconnecting porous structure and surface roughness of the scaffolds. This, in turn, led to successful osteogenic differentiation of hMSCs with improved cell adhesion, proliferation, differentiation, mineralization and expression of pro-osteogenic cellular proteins. This provides huge support for Au(SiO2) as a suitable material in BTE.
URI: https://hdl.handle.net/10356/142380
ISSN: 1661-6596
DOI: 10.3390/ijms20205135
Rights: © 2019 The Authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles

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