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In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering

The selection of a suitable scaffold matrix is critical for cell-based bone tissue engineering. This study aimed to identify and characterize natural marine sponges as potential bioscaffolds for osteogenesis. Callyspongiidae marine sponge samples were collected from the Fremantle coast of Western Au...

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Autores principales: Lin, Zhen, Solomon, Kellie L., Zhang, Xiaoling, Pavlos, Nathan J., Abel, Tamara, Willers, Craig, Dai, Kerong, Xu, Jiake, Zheng, Qiujian, Zheng, Minghao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157271/
https://www.ncbi.nlm.nih.gov/pubmed/21850206
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author Lin, Zhen
Solomon, Kellie L.
Zhang, Xiaoling
Pavlos, Nathan J.
Abel, Tamara
Willers, Craig
Dai, Kerong
Xu, Jiake
Zheng, Qiujian
Zheng, Minghao
author_facet Lin, Zhen
Solomon, Kellie L.
Zhang, Xiaoling
Pavlos, Nathan J.
Abel, Tamara
Willers, Craig
Dai, Kerong
Xu, Jiake
Zheng, Qiujian
Zheng, Minghao
author_sort Lin, Zhen
collection PubMed
description The selection of a suitable scaffold matrix is critical for cell-based bone tissue engineering. This study aimed to identify and characterize natural marine sponges as potential bioscaffolds for osteogenesis. Callyspongiidae marine sponge samples were collected from the Fremantle coast of Western Australia. The sponge structure was assessed using scanning electron microscopy (SEM) and Hematoxylin and eosin. Mouse primary osteoblasts were seeded onto the sponge scaffold and immunostained with F-actin to assess cell attachment and aggregation. Alkaline phosphatase expression, von Kossa staining and real-time PCR were performed to examine the osteogenic potential of sponge samples. SEM revealed that the sponge skeleton possessed a collagenous fibrous network consisting of interconnecting channels and a porous structure that support cellular adhesion, aggregation and growth. The average pore size of the sponge skeleton was measured 100 to 300 μm in diameter. F-actin staining demonstrated that osteoblasts were able to anchor onto the surface of collagen fibres. Alkaline phosphatase expression, a marker of early osteoblast differentiation, was evident at 7 days although expression decreased steadily with long term culture. Using von Kossa staining, mineralisation nodules were evident after 21 days. Gene expression of osteoblast markers, osteocalcin and osteopontin, was also observed at 7, 14 and 21 days of culture. Together, these results suggest that the natural marine sponge is promising as a new scaffold for use in bone tissue engineering.
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spelling pubmed-31572712011-08-17 In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering Lin, Zhen Solomon, Kellie L. Zhang, Xiaoling Pavlos, Nathan J. Abel, Tamara Willers, Craig Dai, Kerong Xu, Jiake Zheng, Qiujian Zheng, Minghao Int J Biol Sci Research Paper The selection of a suitable scaffold matrix is critical for cell-based bone tissue engineering. This study aimed to identify and characterize natural marine sponges as potential bioscaffolds for osteogenesis. Callyspongiidae marine sponge samples were collected from the Fremantle coast of Western Australia. The sponge structure was assessed using scanning electron microscopy (SEM) and Hematoxylin and eosin. Mouse primary osteoblasts were seeded onto the sponge scaffold and immunostained with F-actin to assess cell attachment and aggregation. Alkaline phosphatase expression, von Kossa staining and real-time PCR were performed to examine the osteogenic potential of sponge samples. SEM revealed that the sponge skeleton possessed a collagenous fibrous network consisting of interconnecting channels and a porous structure that support cellular adhesion, aggregation and growth. The average pore size of the sponge skeleton was measured 100 to 300 μm in diameter. F-actin staining demonstrated that osteoblasts were able to anchor onto the surface of collagen fibres. Alkaline phosphatase expression, a marker of early osteoblast differentiation, was evident at 7 days although expression decreased steadily with long term culture. Using von Kossa staining, mineralisation nodules were evident after 21 days. Gene expression of osteoblast markers, osteocalcin and osteopontin, was also observed at 7, 14 and 21 days of culture. Together, these results suggest that the natural marine sponge is promising as a new scaffold for use in bone tissue engineering. Ivyspring International Publisher 2011-08-07 /pmc/articles/PMC3157271/ /pubmed/21850206 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Lin, Zhen
Solomon, Kellie L.
Zhang, Xiaoling
Pavlos, Nathan J.
Abel, Tamara
Willers, Craig
Dai, Kerong
Xu, Jiake
Zheng, Qiujian
Zheng, Minghao
In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering
title In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering
title_full In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering
title_fullStr In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering
title_full_unstemmed In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering
title_short In vitro Evaluation of Natural Marine Sponge Collagen as a Scaffold for Bone Tissue Engineering
title_sort in vitro evaluation of natural marine sponge collagen as a scaffold for bone tissue engineering
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157271/
https://www.ncbi.nlm.nih.gov/pubmed/21850206
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