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Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects()
INTRODUCTION: This study aimed to examine the bone-forming ability of medium-cross-linked recombinant collagen peptide (mRCP) particles developedbased on human collagen type I, contains an arginyl-glycyl-aspartic acid-rich motif, fabricated as bone filling material, compared to that of the autologou...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society for Regenerative Medicine
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773759/ https://www.ncbi.nlm.nih.gov/pubmed/33426238 http://dx.doi.org/10.1016/j.reth.2020.12.001 |
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author | Akiyama, Yasunori Ito, Masaaki Toriumi, Taku Hiratsuka, Takahiro Arai, Yoshinori Tanaka, Sho Futenma, Taku Akiyama, Yuhki Yamaguchi, Kazuhiro Azuma, Akihiko Hata, Ken-ichiro Natsume, Nagato Honda, Masaki |
author_facet | Akiyama, Yasunori Ito, Masaaki Toriumi, Taku Hiratsuka, Takahiro Arai, Yoshinori Tanaka, Sho Futenma, Taku Akiyama, Yuhki Yamaguchi, Kazuhiro Azuma, Akihiko Hata, Ken-ichiro Natsume, Nagato Honda, Masaki |
author_sort | Akiyama, Yasunori |
collection | PubMed |
description | INTRODUCTION: This study aimed to examine the bone-forming ability of medium-cross-linked recombinant collagen peptide (mRCP) particles developedbased on human collagen type I, contains an arginyl-glycyl-aspartic acid-rich motif, fabricated as bone filling material, compared to that of the autologous bone graft. METHODS: Calvarial bone defects were created in immunodeficient rats though a surgical procedure. The rats were divided into 2 groups: mRCP graft and tibia bone graft (bone graft). The bone formation potential of mRCP was evaluated by micro-computed tomography and hematoxylin-eosin staining at 1, 2, 3, and 4 weeks after surgery, and the data were analyzed and compared to those of the bone graft. RESULTS: The axial volume-rendered images demonstrated considerable bony bridging with the mRCP graft, but there was no significant difference in the bone volume and bone mineral density between the mRCP graft and bone graft at 4 weeks. The peripheral new bone density was significantly higher than the central new bone density and the bottom side score was significantly higher than the top side score at early stage in the regenerated bone within the bone defects. CONCLUSION: These results indicate that mRCP has a high potential of recruiting osteogenic cells, comparable to that of autologous bone chips. |
format | Online Article Text |
id | pubmed-7773759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Japanese Society for Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-77737592021-01-08 Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects() Akiyama, Yasunori Ito, Masaaki Toriumi, Taku Hiratsuka, Takahiro Arai, Yoshinori Tanaka, Sho Futenma, Taku Akiyama, Yuhki Yamaguchi, Kazuhiro Azuma, Akihiko Hata, Ken-ichiro Natsume, Nagato Honda, Masaki Regen Ther Original Article INTRODUCTION: This study aimed to examine the bone-forming ability of medium-cross-linked recombinant collagen peptide (mRCP) particles developedbased on human collagen type I, contains an arginyl-glycyl-aspartic acid-rich motif, fabricated as bone filling material, compared to that of the autologous bone graft. METHODS: Calvarial bone defects were created in immunodeficient rats though a surgical procedure. The rats were divided into 2 groups: mRCP graft and tibia bone graft (bone graft). The bone formation potential of mRCP was evaluated by micro-computed tomography and hematoxylin-eosin staining at 1, 2, 3, and 4 weeks after surgery, and the data were analyzed and compared to those of the bone graft. RESULTS: The axial volume-rendered images demonstrated considerable bony bridging with the mRCP graft, but there was no significant difference in the bone volume and bone mineral density between the mRCP graft and bone graft at 4 weeks. The peripheral new bone density was significantly higher than the central new bone density and the bottom side score was significantly higher than the top side score at early stage in the regenerated bone within the bone defects. CONCLUSION: These results indicate that mRCP has a high potential of recruiting osteogenic cells, comparable to that of autologous bone chips. Japanese Society for Regenerative Medicine 2020-12-24 /pmc/articles/PMC7773759/ /pubmed/33426238 http://dx.doi.org/10.1016/j.reth.2020.12.001 Text en © 2020 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Akiyama, Yasunori Ito, Masaaki Toriumi, Taku Hiratsuka, Takahiro Arai, Yoshinori Tanaka, Sho Futenma, Taku Akiyama, Yuhki Yamaguchi, Kazuhiro Azuma, Akihiko Hata, Ken-ichiro Natsume, Nagato Honda, Masaki Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects() |
title | Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects() |
title_full | Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects() |
title_fullStr | Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects() |
title_full_unstemmed | Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects() |
title_short | Bone formation potential of collagen type I-based recombinant peptide particles in rat calvaria defects() |
title_sort | bone formation potential of collagen type i-based recombinant peptide particles in rat calvaria defects() |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773759/ https://www.ncbi.nlm.nih.gov/pubmed/33426238 http://dx.doi.org/10.1016/j.reth.2020.12.001 |
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