Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2020
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
_version_ 1783630115449602048
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
work_keys_str_mv AT akiyamayasunori boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT itomasaaki boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT toriumitaku boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT hiratsukatakahiro boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT araiyoshinori boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT tanakasho boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT futenmataku boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT akiyamayuhki boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT yamaguchikazuhiro boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT azumaakihiko boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT hatakenichiro boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT natsumenagato boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects
AT hondamasaki boneformationpotentialofcollagentypeibasedrecombinantpeptideparticlesinratcalvariadefects