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Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury

Brain-derived neurotrophic factor (BDNF), which is released due to nerve injury, is known to promote the natural healing of injured nerves. It is often observed that damage of mandibular canal induces local sclerotic changes in alveolar bone. We reported that peripheral nerve injury promotes the loc...

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Autores principales: Ida-Yonemochi, Hiroko, Yamada, Yurie, Yoshikawa, Hiroyuki, Seo, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224970/
https://www.ncbi.nlm.nih.gov/pubmed/28072837
http://dx.doi.org/10.1371/journal.pone.0169201
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author Ida-Yonemochi, Hiroko
Yamada, Yurie
Yoshikawa, Hiroyuki
Seo, Kenji
author_facet Ida-Yonemochi, Hiroko
Yamada, Yurie
Yoshikawa, Hiroyuki
Seo, Kenji
author_sort Ida-Yonemochi, Hiroko
collection PubMed
description Brain-derived neurotrophic factor (BDNF), which is released due to nerve injury, is known to promote the natural healing of injured nerves. It is often observed that damage of mandibular canal induces local sclerotic changes in alveolar bone. We reported that peripheral nerve injury promotes the local production of BDNF; therefore, it was possible to hypothesize that peripheral nerve injury affects sclerotic changes in the alveolar bone. This study aimed to evaluate the effect of BDNF on osteogenesis using in vitro osteoblast-lineage cell culture and an in vivo rat osteotomy model. MC3T3-E1 cells were cultured with BDNF and were examined for cell proliferative activity, chemotaxis and mRNA expression levels of osteoblast differentiation markers. For in vivo study, inferior alveolar nerve (IAN) injury experiments and mandibular cortical osteotomy were performed using a rat model. In the osteotomy model, exogenous BDNF was applied to bone surfaces after corticotomy of the mandible, and we morphologically analyzed the new bone formation. As a result, mRNA expression of osteoblast differentiation marker, osteocalcin, was significantly increased by BDNF, although cell proliferation and migration were not affected. In the in vivo study, osteopontin-positive new bone formation was significantly accelerated in the BDNF-grafted groups, and active bone remodeling, involving trkB-positive osteoblasts and osteocytes, continued after 28 days. In conclusion, BDNF stimulated the differentiation of MC3T3-E1 cells and it promoted new bone formation and maturation. These results suggested that local BDNF produced by peripheral nerve injury contributes to accelerating sclerotic changes in the alveolar bone.
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spelling pubmed-52249702017-01-31 Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury Ida-Yonemochi, Hiroko Yamada, Yurie Yoshikawa, Hiroyuki Seo, Kenji PLoS One Research Article Brain-derived neurotrophic factor (BDNF), which is released due to nerve injury, is known to promote the natural healing of injured nerves. It is often observed that damage of mandibular canal induces local sclerotic changes in alveolar bone. We reported that peripheral nerve injury promotes the local production of BDNF; therefore, it was possible to hypothesize that peripheral nerve injury affects sclerotic changes in the alveolar bone. This study aimed to evaluate the effect of BDNF on osteogenesis using in vitro osteoblast-lineage cell culture and an in vivo rat osteotomy model. MC3T3-E1 cells were cultured with BDNF and were examined for cell proliferative activity, chemotaxis and mRNA expression levels of osteoblast differentiation markers. For in vivo study, inferior alveolar nerve (IAN) injury experiments and mandibular cortical osteotomy were performed using a rat model. In the osteotomy model, exogenous BDNF was applied to bone surfaces after corticotomy of the mandible, and we morphologically analyzed the new bone formation. As a result, mRNA expression of osteoblast differentiation marker, osteocalcin, was significantly increased by BDNF, although cell proliferation and migration were not affected. In the in vivo study, osteopontin-positive new bone formation was significantly accelerated in the BDNF-grafted groups, and active bone remodeling, involving trkB-positive osteoblasts and osteocytes, continued after 28 days. In conclusion, BDNF stimulated the differentiation of MC3T3-E1 cells and it promoted new bone formation and maturation. These results suggested that local BDNF produced by peripheral nerve injury contributes to accelerating sclerotic changes in the alveolar bone. Public Library of Science 2017-01-10 /pmc/articles/PMC5224970/ /pubmed/28072837 http://dx.doi.org/10.1371/journal.pone.0169201 Text en © 2017 Ida-Yonemochi 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
Ida-Yonemochi, Hiroko
Yamada, Yurie
Yoshikawa, Hiroyuki
Seo, Kenji
Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury
title Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury
title_full Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury
title_fullStr Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury
title_full_unstemmed Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury
title_short Locally Produced BDNF Promotes Sclerotic Change in Alveolar Bone after Nerve Injury
title_sort locally produced bdnf promotes sclerotic change in alveolar bone after nerve injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224970/
https://www.ncbi.nlm.nih.gov/pubmed/28072837
http://dx.doi.org/10.1371/journal.pone.0169201
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