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Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites
Recently, graphene-based nanomaterials, in the form of two dimensional substrates or three dimensional foams, have attracted considerable attention as bioactive scaffolds to promote the differentiation of various stem cells towards specific lineages. On the other hand, the potential advantages of us...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685392/ https://www.ncbi.nlm.nih.gov/pubmed/26685901 http://dx.doi.org/10.1038/srep18833 |
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author | Lee, Jong Ho Shin, Yong Cheol Lee, Sang-Min Jin, Oh Seong Kang, Seok Hee Hong, Suck Won Jeong, Chang-Mo Huh, Jung Bo Han, Dong-Wook |
author_facet | Lee, Jong Ho Shin, Yong Cheol Lee, Sang-Min Jin, Oh Seong Kang, Seok Hee Hong, Suck Won Jeong, Chang-Mo Huh, Jung Bo Han, Dong-Wook |
author_sort | Lee, Jong Ho |
collection | PubMed |
description | Recently, graphene-based nanomaterials, in the form of two dimensional substrates or three dimensional foams, have attracted considerable attention as bioactive scaffolds to promote the differentiation of various stem cells towards specific lineages. On the other hand, the potential advantages of using graphene-based hybrid composites directly as factors inducing cellular differentiation as well as tissue regeneration are unclear. This study examined whether nanocomposites of reduced graphene oxide (rGO) and hydroxyapatite (HAp) (rGO/HAp NCs) could enhance the osteogenesis of MC3T3-E1 preosteoblasts and promote new bone formation. When combined with HAp, rGO synergistically promoted the spontaneous osteodifferentiation of MC3T3-E1 cells without hindering their proliferation. This enhanced osteogenesis was corroborated from determination of alkaline phosphatase activity as early stage markers of osteodifferentiation and mineralization of calcium and phosphate as late stage markers. Immunoblot analysis showed that rGO/HAp NCs increase the expression levels of osteopontin and osteocalcin significantly. Furthermore, rGO/HAp grafts were found to significantly enhance new bone formation in full-thickness calvarial defects without inflammatory responses. These results suggest that rGO/HAp NCs can be exploited to craft a range of strategies for the development of novel dental and orthopedic bone grafts to accelerate bone regeneration because these graphene-based composite materials have potentials to stimulate osteogenesis. |
format | Online Article Text |
id | pubmed-4685392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46853922015-12-30 Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites Lee, Jong Ho Shin, Yong Cheol Lee, Sang-Min Jin, Oh Seong Kang, Seok Hee Hong, Suck Won Jeong, Chang-Mo Huh, Jung Bo Han, Dong-Wook Sci Rep Article Recently, graphene-based nanomaterials, in the form of two dimensional substrates or three dimensional foams, have attracted considerable attention as bioactive scaffolds to promote the differentiation of various stem cells towards specific lineages. On the other hand, the potential advantages of using graphene-based hybrid composites directly as factors inducing cellular differentiation as well as tissue regeneration are unclear. This study examined whether nanocomposites of reduced graphene oxide (rGO) and hydroxyapatite (HAp) (rGO/HAp NCs) could enhance the osteogenesis of MC3T3-E1 preosteoblasts and promote new bone formation. When combined with HAp, rGO synergistically promoted the spontaneous osteodifferentiation of MC3T3-E1 cells without hindering their proliferation. This enhanced osteogenesis was corroborated from determination of alkaline phosphatase activity as early stage markers of osteodifferentiation and mineralization of calcium and phosphate as late stage markers. Immunoblot analysis showed that rGO/HAp NCs increase the expression levels of osteopontin and osteocalcin significantly. Furthermore, rGO/HAp grafts were found to significantly enhance new bone formation in full-thickness calvarial defects without inflammatory responses. These results suggest that rGO/HAp NCs can be exploited to craft a range of strategies for the development of novel dental and orthopedic bone grafts to accelerate bone regeneration because these graphene-based composite materials have potentials to stimulate osteogenesis. Nature Publishing Group 2015-12-21 /pmc/articles/PMC4685392/ /pubmed/26685901 http://dx.doi.org/10.1038/srep18833 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lee, Jong Ho Shin, Yong Cheol Lee, Sang-Min Jin, Oh Seong Kang, Seok Hee Hong, Suck Won Jeong, Chang-Mo Huh, Jung Bo Han, Dong-Wook Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites |
title | Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites |
title_full | Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites |
title_fullStr | Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites |
title_full_unstemmed | Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites |
title_short | Enhanced Osteogenesis by Reduced Graphene Oxide/Hydroxyapatite Nanocomposites |
title_sort | enhanced osteogenesis by reduced graphene oxide/hydroxyapatite nanocomposites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685392/ https://www.ncbi.nlm.nih.gov/pubmed/26685901 http://dx.doi.org/10.1038/srep18833 |
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