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The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation
INTRODUCTION: Deproteinized bovine bone mineral (Bio-Oss) is a xenogenic bone substitute, widely used in maxillofacial bone regeneration. The aim of this in vitro study was to investigate its influence on the growth behavior of human osteosarcoma cell line, Saos-2 culture, and compare it with the ph...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Center for Endodontic Research
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734514/ https://www.ncbi.nlm.nih.gov/pubmed/23922573 |
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author | Khojasteh, Arash Ghahremani, Mohammad Hossein Ostad, Seyed Nasser Eslami, Mohammad Motahhary, Pourya Morad, Golnaz Shidfar, Shireen |
author_facet | Khojasteh, Arash Ghahremani, Mohammad Hossein Ostad, Seyed Nasser Eslami, Mohammad Motahhary, Pourya Morad, Golnaz Shidfar, Shireen |
author_sort | Khojasteh, Arash |
collection | PubMed |
description | INTRODUCTION: Deproteinized bovine bone mineral (Bio-Oss) is a xenogenic bone substitute, widely used in maxillofacial bone regeneration. The aim of this in vitro study was to investigate its influence on the growth behavior of human osteosarcoma cell line, Saos-2 culture, and compare it with the physiologic dose of Dexamethasone, an inductive factor for osteoblasts. MATERIALS AND METHODS: Human osteosarcoma cells, Saos-2, were cultured on Bio-Oss and their growth rate was compared to Saos-2 cultures treated with Dexamethasone 10(-7) M in contrast to cells cultivated in PBS, in the control group. Assessment of proliferation was performed after 24, 36, and 48 hours by counting cells using trypan blue exclusion method. Alkaline phosphatase was measured spectrophotometrically at 405 nm with paranitrophenol buffer. RESULTS: After 48 hours, the number of Saos-2 cells increased significantly when subcultured with Bio-Oss. Bio-Oss was more effective on the enhancement of proliferation of Saos-2 cells when compared to the physiologic dose of Dexamethasone (P<0.05). Alkaline phosphatase activity increased in cells grown on Bio-Oss and dexamethasone 10(-7) M in contrast to cells cultivated in PBS control group. The greatest level of activity was observed in the group containing Bio-Oss after 48 hour. CONCLUSION: The significant increase of cell proliferation and alkaline phosphatase activity in cells cultured on Bio-Oss, compared to Dexamethasone-treated cells, suggests the important role of this bone substitute in promoting bone regeneration. |
format | Online Article Text |
id | pubmed-3734514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Iranian Center for Endodontic Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-37345142013-08-06 The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation Khojasteh, Arash Ghahremani, Mohammad Hossein Ostad, Seyed Nasser Eslami, Mohammad Motahhary, Pourya Morad, Golnaz Shidfar, Shireen Iran Endod J Original Article INTRODUCTION: Deproteinized bovine bone mineral (Bio-Oss) is a xenogenic bone substitute, widely used in maxillofacial bone regeneration. The aim of this in vitro study was to investigate its influence on the growth behavior of human osteosarcoma cell line, Saos-2 culture, and compare it with the physiologic dose of Dexamethasone, an inductive factor for osteoblasts. MATERIALS AND METHODS: Human osteosarcoma cells, Saos-2, were cultured on Bio-Oss and their growth rate was compared to Saos-2 cultures treated with Dexamethasone 10(-7) M in contrast to cells cultivated in PBS, in the control group. Assessment of proliferation was performed after 24, 36, and 48 hours by counting cells using trypan blue exclusion method. Alkaline phosphatase was measured spectrophotometrically at 405 nm with paranitrophenol buffer. RESULTS: After 48 hours, the number of Saos-2 cells increased significantly when subcultured with Bio-Oss. Bio-Oss was more effective on the enhancement of proliferation of Saos-2 cells when compared to the physiologic dose of Dexamethasone (P<0.05). Alkaline phosphatase activity increased in cells grown on Bio-Oss and dexamethasone 10(-7) M in contrast to cells cultivated in PBS control group. The greatest level of activity was observed in the group containing Bio-Oss after 48 hour. CONCLUSION: The significant increase of cell proliferation and alkaline phosphatase activity in cells cultured on Bio-Oss, compared to Dexamethasone-treated cells, suggests the important role of this bone substitute in promoting bone regeneration. Iranian Center for Endodontic Research 2013-08-01 2013 /pmc/articles/PMC3734514/ /pubmed/23922573 Text en Copyright © 2013, Iranian Endodontic Journal. http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Khojasteh, Arash Ghahremani, Mohammad Hossein Ostad, Seyed Nasser Eslami, Mohammad Motahhary, Pourya Morad, Golnaz Shidfar, Shireen The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation |
title | The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation |
title_full | The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation |
title_fullStr | The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation |
title_full_unstemmed | The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation |
title_short | The Effect of Deproteinized Bovine Bone Mineral on Saos-2 Cell Proliferation |
title_sort | effect of deproteinized bovine bone mineral on saos-2 cell proliferation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734514/ https://www.ncbi.nlm.nih.gov/pubmed/23922573 |
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