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In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications

BACKGROUND: The receptor activator of nuclear factor kappa-B (RANK)/RANK ligand/osteoprotegerin (OPG) system plays a critical role in bone remodelling by regulating osteoclast formation and activity. OPG has been used systemically in the treatment of bone diseases. In searching for more effective an...

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Autores principales: Jayash, Soher Nagi, Hashim, Najihah M., Misran, Misni, Baharuddin, NA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012333/
https://www.ncbi.nlm.nih.gov/pubmed/27635307
http://dx.doi.org/10.7717/peerj.2229
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author Jayash, Soher Nagi
Hashim, Najihah M.
Misran, Misni
Baharuddin, NA
author_facet Jayash, Soher Nagi
Hashim, Najihah M.
Misran, Misni
Baharuddin, NA
author_sort Jayash, Soher Nagi
collection PubMed
description BACKGROUND: The receptor activator of nuclear factor kappa-B (RANK)/RANK ligand/osteoprotegerin (OPG) system plays a critical role in bone remodelling by regulating osteoclast formation and activity. OPG has been used systemically in the treatment of bone diseases. In searching for more effective and safer treatment for bone diseases, we investigated newly formulated OPG-chitosan complexes, which is prepared as a local application for its osteogenic potential to remediate bone defects. METHODS: We examined high, medium and low molecular weights of chitosan combined with OPG. The cytotoxicity of OPG in chitosan and its proliferation in vitro was evaluated using normal, human periodontal ligament (NHPL) fibroblasts in 2D and 3D cell culture. The cytotoxicity of these combinations was compared by measuring cell survival with a tetrazolium salt reduction (MTT) assay and AlamarBlue assay. The cellular morphological changes were observed under an inverted microscope. A propidium iodide and acridine orange double-staining assay was used to evaluate the morphology and quantify the viable and nonviable cells. The expression level of osteopontin and osteocalcin protein in treated normal human osteoblast cells was evaluated by using Western blot. RESULTS: The results demonstrated that OPG in combination with chitosan was non-toxic, and OPG combined with low molecular weight chitosan has the most significant effect on NHPL fibroblasts and stimulates proliferation of cells over the period of treatment.
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spelling pubmed-50123332016-09-15 In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications Jayash, Soher Nagi Hashim, Najihah M. Misran, Misni Baharuddin, NA PeerJ Bioengineering BACKGROUND: The receptor activator of nuclear factor kappa-B (RANK)/RANK ligand/osteoprotegerin (OPG) system plays a critical role in bone remodelling by regulating osteoclast formation and activity. OPG has been used systemically in the treatment of bone diseases. In searching for more effective and safer treatment for bone diseases, we investigated newly formulated OPG-chitosan complexes, which is prepared as a local application for its osteogenic potential to remediate bone defects. METHODS: We examined high, medium and low molecular weights of chitosan combined with OPG. The cytotoxicity of OPG in chitosan and its proliferation in vitro was evaluated using normal, human periodontal ligament (NHPL) fibroblasts in 2D and 3D cell culture. The cytotoxicity of these combinations was compared by measuring cell survival with a tetrazolium salt reduction (MTT) assay and AlamarBlue assay. The cellular morphological changes were observed under an inverted microscope. A propidium iodide and acridine orange double-staining assay was used to evaluate the morphology and quantify the viable and nonviable cells. The expression level of osteopontin and osteocalcin protein in treated normal human osteoblast cells was evaluated by using Western blot. RESULTS: The results demonstrated that OPG in combination with chitosan was non-toxic, and OPG combined with low molecular weight chitosan has the most significant effect on NHPL fibroblasts and stimulates proliferation of cells over the period of treatment. PeerJ Inc. 2016-08-23 /pmc/articles/PMC5012333/ /pubmed/27635307 http://dx.doi.org/10.7717/peerj.2229 Text en ©2016 Jayash et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioengineering
Jayash, Soher Nagi
Hashim, Najihah M.
Misran, Misni
Baharuddin, NA
In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications
title In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications
title_full In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications
title_fullStr In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications
title_full_unstemmed In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications
title_short In vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications
title_sort in vitro evaluation of osteoprotegerin in chitosan for potential bone defect applications
topic Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012333/
https://www.ncbi.nlm.nih.gov/pubmed/27635307
http://dx.doi.org/10.7717/peerj.2229
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