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Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration

The initial step of bone regeneration requires the migration of osteogenic cells to defective sites. Our previous studies suggest that a salmon DNA-based scaffold can promote the bone regeneration of calvarial defects in rats. We speculate that the salmon DNA may possess osteoinductive properties, i...

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Autores principales: Sato, Ayako, Kajiya, Hiroshi, Mori, Nana, Sato, Hironobu, Fukushima, Tadao, Kido, Hirofumi, Ohno, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5218488/
https://www.ncbi.nlm.nih.gov/pubmed/28060874
http://dx.doi.org/10.1371/journal.pone.0169522
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author Sato, Ayako
Kajiya, Hiroshi
Mori, Nana
Sato, Hironobu
Fukushima, Tadao
Kido, Hirofumi
Ohno, Jun
author_facet Sato, Ayako
Kajiya, Hiroshi
Mori, Nana
Sato, Hironobu
Fukushima, Tadao
Kido, Hirofumi
Ohno, Jun
author_sort Sato, Ayako
collection PubMed
description The initial step of bone regeneration requires the migration of osteogenic cells to defective sites. Our previous studies suggest that a salmon DNA-based scaffold can promote the bone regeneration of calvarial defects in rats. We speculate that the salmon DNA may possess osteoinductive properties, including the homing of migrating osteogenic cells. In the present study, we investigated the influence of the salmon DNA on osteoblastic differentiation and induction of osteoblast migration using MG63 cells (human preosteoblasts) in vitro. Moreover, we analyzed the bone regeneration of a critical-sized in vivo calvarial bone defect (CSD) model in rats. The salmon DNA enhanced both mRNA and protein expression of the osteogenesis-related factors, runt-related transcription factor 2 (Runx2), alkaline phosphatase, and osterix (OSX) in the MG63 cells, compared with the cultivation using osteogenic induction medium alone. From the histochemical and immunohistochemical assays using frozen sections of the bone defects from animals that were implanted with DNA disks, many cells were found to express aldehyde dehydrogenase 1, one of the markers for mesenchymal stem cells. In addition, OSX was observed in the replaced connective tissue of the bone defects. These findings indicate that the DNA induced the migration and accumulation of osteogenic cells to the regenerative tissue. Furthermore, an in vitro transwell migration assay showed that the addition of DNA enhanced an induction of osteoblast migration, compared with the medium alone. The implantation of the DNA disks promoted bone regeneration in the CSD of rats, compared with that of collagen disks. These results indicate that the salmon DNA enhanced osteoblastic differentiation and induction of migration, resulting in the facilitation of bone regeneration.
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spelling pubmed-52184882017-01-19 Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration Sato, Ayako Kajiya, Hiroshi Mori, Nana Sato, Hironobu Fukushima, Tadao Kido, Hirofumi Ohno, Jun PLoS One Research Article The initial step of bone regeneration requires the migration of osteogenic cells to defective sites. Our previous studies suggest that a salmon DNA-based scaffold can promote the bone regeneration of calvarial defects in rats. We speculate that the salmon DNA may possess osteoinductive properties, including the homing of migrating osteogenic cells. In the present study, we investigated the influence of the salmon DNA on osteoblastic differentiation and induction of osteoblast migration using MG63 cells (human preosteoblasts) in vitro. Moreover, we analyzed the bone regeneration of a critical-sized in vivo calvarial bone defect (CSD) model in rats. The salmon DNA enhanced both mRNA and protein expression of the osteogenesis-related factors, runt-related transcription factor 2 (Runx2), alkaline phosphatase, and osterix (OSX) in the MG63 cells, compared with the cultivation using osteogenic induction medium alone. From the histochemical and immunohistochemical assays using frozen sections of the bone defects from animals that were implanted with DNA disks, many cells were found to express aldehyde dehydrogenase 1, one of the markers for mesenchymal stem cells. In addition, OSX was observed in the replaced connective tissue of the bone defects. These findings indicate that the DNA induced the migration and accumulation of osteogenic cells to the regenerative tissue. Furthermore, an in vitro transwell migration assay showed that the addition of DNA enhanced an induction of osteoblast migration, compared with the medium alone. The implantation of the DNA disks promoted bone regeneration in the CSD of rats, compared with that of collagen disks. These results indicate that the salmon DNA enhanced osteoblastic differentiation and induction of migration, resulting in the facilitation of bone regeneration. Public Library of Science 2017-01-06 /pmc/articles/PMC5218488/ /pubmed/28060874 http://dx.doi.org/10.1371/journal.pone.0169522 Text en © 2017 Sato 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, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sato, Ayako
Kajiya, Hiroshi
Mori, Nana
Sato, Hironobu
Fukushima, Tadao
Kido, Hirofumi
Ohno, Jun
Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration
title Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration
title_full Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration
title_fullStr Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration
title_full_unstemmed Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration
title_short Salmon DNA Accelerates Bone Regeneration by Inducing Osteoblast Migration
title_sort salmon dna accelerates bone regeneration by inducing osteoblast migration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5218488/
https://www.ncbi.nlm.nih.gov/pubmed/28060874
http://dx.doi.org/10.1371/journal.pone.0169522
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