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Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis

Bone marrow ablation prompts transient bone formation in nearly the entire medullary cavity before marrow regeneration occurs. Here, we establish a procedure to direct bone formation in a desired particular site within the medullary cavity for support of biomedical devices. Local intramedullary inju...

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Autores principales: Miyazaki-Asato, Yoko, Koi, Kiyono, Fujimoto, Hiroki, Kakura, Kae, Kido, Hirofumi, Yanagi, Tsukasa, Yamashita, Junro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804436/
https://www.ncbi.nlm.nih.gov/pubmed/33436871
http://dx.doi.org/10.1038/s41598-020-80316-y
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author Miyazaki-Asato, Yoko
Koi, Kiyono
Fujimoto, Hiroki
Kakura, Kae
Kido, Hirofumi
Yanagi, Tsukasa
Yamashita, Junro
author_facet Miyazaki-Asato, Yoko
Koi, Kiyono
Fujimoto, Hiroki
Kakura, Kae
Kido, Hirofumi
Yanagi, Tsukasa
Yamashita, Junro
author_sort Miyazaki-Asato, Yoko
collection PubMed
description Bone marrow ablation prompts transient bone formation in nearly the entire medullary cavity before marrow regeneration occurs. Here, we establish a procedure to direct bone formation in a desired particular site within the medullary cavity for support of biomedical devices. Local intramedullary injury was performed in the tibiae of rats and parathyroid hormone (PTH), alendronate, or saline was administered. Newly generated bone in the medulla was assessed by micro-CT and histology. To evaluate the function of newly generated bone, animals received intramedullary injury in tibiae followed by daily PTH. At day-14, implants were placed in the endocortical bone and the bone response to the implants was assessed. The fate of newly generated bone was compared with and without implants. We found that neither intramedullary injury nor medication alone resulted in bone formation. However, when combined, substantial bone was generated locally inside the diaphyseal medulla. Newly formed bone disappeared without implant placement but was retained with implants. Bone was especially retained around and between the implants. This study found that local bone marrow disruption followed by PTH or alendronate generated substantial cancellous bone locally in the diaphyseal medulla. This approach offers promise as a tissue engineering tool in medicine and dentistry.
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spelling pubmed-78044362021-01-13 Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis Miyazaki-Asato, Yoko Koi, Kiyono Fujimoto, Hiroki Kakura, Kae Kido, Hirofumi Yanagi, Tsukasa Yamashita, Junro Sci Rep Article Bone marrow ablation prompts transient bone formation in nearly the entire medullary cavity before marrow regeneration occurs. Here, we establish a procedure to direct bone formation in a desired particular site within the medullary cavity for support of biomedical devices. Local intramedullary injury was performed in the tibiae of rats and parathyroid hormone (PTH), alendronate, or saline was administered. Newly generated bone in the medulla was assessed by micro-CT and histology. To evaluate the function of newly generated bone, animals received intramedullary injury in tibiae followed by daily PTH. At day-14, implants were placed in the endocortical bone and the bone response to the implants was assessed. The fate of newly generated bone was compared with and without implants. We found that neither intramedullary injury nor medication alone resulted in bone formation. However, when combined, substantial bone was generated locally inside the diaphyseal medulla. Newly formed bone disappeared without implant placement but was retained with implants. Bone was especially retained around and between the implants. This study found that local bone marrow disruption followed by PTH or alendronate generated substantial cancellous bone locally in the diaphyseal medulla. This approach offers promise as a tissue engineering tool in medicine and dentistry. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804436/ /pubmed/33436871 http://dx.doi.org/10.1038/s41598-020-80316-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Miyazaki-Asato, Yoko
Koi, Kiyono
Fujimoto, Hiroki
Kakura, Kae
Kido, Hirofumi
Yanagi, Tsukasa
Yamashita, Junro
Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis
title Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis
title_full Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis
title_fullStr Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis
title_full_unstemmed Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis
title_short Intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis
title_sort intramedullary injury combined with osteoporosis therapeutics regulates targeted local osteogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804436/
https://www.ncbi.nlm.nih.gov/pubmed/33436871
http://dx.doi.org/10.1038/s41598-020-80316-y
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