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Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix

AIM: The aim of this study was to generate composite bone graft and investigate the rabbit fetal osteoblasts adhesion, proliferation and penetration on acellular matrices of cancellous bone. MATERIALS AND METHODS: Acellular cancellous bone was prepared and developed as in the previous study with lit...

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Autores principales: Rashmi, Pathak, Rekha, Amarpal, Aithal, H. P., Kinjavdekar, P., Pawde, A. M., Tiwari, A. K., Sangeetha, P., Tamilmahan, P., Manzoor, A. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Veterinary World 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352840/
https://www.ncbi.nlm.nih.gov/pubmed/28344398
http://dx.doi.org/10.14202/vetworld.2017.163-169
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author Rashmi,
Pathak, Rekha
Amarpal,
Aithal, H. P.
Kinjavdekar, P.
Pawde, A. M.
Tiwari, A. K.
Sangeetha, P.
Tamilmahan, P.
Manzoor, A. B.
author_facet Rashmi,
Pathak, Rekha
Amarpal,
Aithal, H. P.
Kinjavdekar, P.
Pawde, A. M.
Tiwari, A. K.
Sangeetha, P.
Tamilmahan, P.
Manzoor, A. B.
author_sort Rashmi,
collection PubMed
description AIM: The aim of this study was to generate composite bone graft and investigate the rabbit fetal osteoblasts adhesion, proliferation and penetration on acellular matrices of cancellous bone. MATERIALS AND METHODS: Acellular cancellous bone was prepared and developed as in the previous study with little modification. These matrices were decellularized by rapid freeze and thaw cycle. To remove the cell debris, they were then treated with hydrogen peroxide (3%) and ethanol to remove antigenic cellular and nuclear materials from the scaffold. Primary osteoblast cells were harvested from 20 to 22 days old rabbit fetal long and calvarial bone. These cells were cultured and characterized using a specific marker. The third passaged fetal osteoblast cells were then seeded on the scaffold and incubated for 14 days. The growth pattern of the cells was observed. Scanning electron microscope and hematoxylin and eosin staining were used to investigate cells proliferation. RESULTS: The cells were found to be growing well on the surface of the scaffold and were also present in good numbers with the matrix filopodial extensions upto inside of the core of the tissue. CONCLUSION: Thus, a viable composite scaffold of bone could be developed which has a great potential in the field of bone tissue engineering.
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spelling pubmed-53528402017-03-24 Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix Rashmi, Pathak, Rekha Amarpal, Aithal, H. P. Kinjavdekar, P. Pawde, A. M. Tiwari, A. K. Sangeetha, P. Tamilmahan, P. Manzoor, A. B. Vet World Research Article AIM: The aim of this study was to generate composite bone graft and investigate the rabbit fetal osteoblasts adhesion, proliferation and penetration on acellular matrices of cancellous bone. MATERIALS AND METHODS: Acellular cancellous bone was prepared and developed as in the previous study with little modification. These matrices were decellularized by rapid freeze and thaw cycle. To remove the cell debris, they were then treated with hydrogen peroxide (3%) and ethanol to remove antigenic cellular and nuclear materials from the scaffold. Primary osteoblast cells were harvested from 20 to 22 days old rabbit fetal long and calvarial bone. These cells were cultured and characterized using a specific marker. The third passaged fetal osteoblast cells were then seeded on the scaffold and incubated for 14 days. The growth pattern of the cells was observed. Scanning electron microscope and hematoxylin and eosin staining were used to investigate cells proliferation. RESULTS: The cells were found to be growing well on the surface of the scaffold and were also present in good numbers with the matrix filopodial extensions upto inside of the core of the tissue. CONCLUSION: Thus, a viable composite scaffold of bone could be developed which has a great potential in the field of bone tissue engineering. Veterinary World 2017-02 2017-02-08 /pmc/articles/PMC5352840/ /pubmed/28344398 http://dx.doi.org/10.14202/vetworld.2017.163-169 Text en Copyright: © Rashmi, et al. http://creativecommons.org/licenses/by/4.0 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Rashmi,
Pathak, Rekha
Amarpal,
Aithal, H. P.
Kinjavdekar, P.
Pawde, A. M.
Tiwari, A. K.
Sangeetha, P.
Tamilmahan, P.
Manzoor, A. B.
Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix
title Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix
title_full Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix
title_fullStr Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix
title_full_unstemmed Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix
title_short Evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix
title_sort evaluation of tissue-engineered bone constructs using rabbit fetal osteoblasts on acellular bovine cancellous bone matrix
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352840/
https://www.ncbi.nlm.nih.gov/pubmed/28344398
http://dx.doi.org/10.14202/vetworld.2017.163-169
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