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Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development
Bone growth is linked to expansion of nearby organs, as is the case for the cranial base and the brain. Here, we focused on development of the mouse clivus, a sloping surface of the basioccipital bone, to define mechanisms underlying morphological changes in bone in response to brain enlargement. Hi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374512/ https://www.ncbi.nlm.nih.gov/pubmed/30760811 http://dx.doi.org/10.1038/s41598-018-38471-w |
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author | Edamoto, Mio Kuroda, Yukiko Yoda, Masaki Kawaai, Katsuhiro Matsuo, Koichi |
author_facet | Edamoto, Mio Kuroda, Yukiko Yoda, Masaki Kawaai, Katsuhiro Matsuo, Koichi |
author_sort | Edamoto, Mio |
collection | PubMed |
description | Bone growth is linked to expansion of nearby organs, as is the case for the cranial base and the brain. Here, we focused on development of the mouse clivus, a sloping surface of the basioccipital bone, to define mechanisms underlying morphological changes in bone in response to brain enlargement. Histological analysis indicated that both endocranial and ectocranial cortical bone layers in the basioccipital carry the osteoclast surface dorsally and the osteoblast surface ventrally. Finite element analysis of mechanical stress on the clivus revealed that compressive and tensile stresses appeared mainly on respective dorsal and ventral surfaces of the basioccipital bone. Osteoclastic bone resorption occurred primarily in the compression area, whereas areas of bone formation largely coincided with the tension area. These data collectively suggest that compressive and tensile stresses govern respective localization of osteoclasts and osteoblasts. Developmental analysis of the basioccipital bone revealed the clivus to be angled in early postnatal wild-type mice, whereas its slope was less prominent in Tnfsf11(−/−) mice, which lack osteoclasts. We propose that osteoclast-osteoblast “trans-pairing” across cortical bone is primarily induced by mechanical stress from growing organs and regulates shape and size of bones that encase the brain. |
format | Online Article Text |
id | pubmed-6374512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63745122019-02-19 Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development Edamoto, Mio Kuroda, Yukiko Yoda, Masaki Kawaai, Katsuhiro Matsuo, Koichi Sci Rep Article Bone growth is linked to expansion of nearby organs, as is the case for the cranial base and the brain. Here, we focused on development of the mouse clivus, a sloping surface of the basioccipital bone, to define mechanisms underlying morphological changes in bone in response to brain enlargement. Histological analysis indicated that both endocranial and ectocranial cortical bone layers in the basioccipital carry the osteoclast surface dorsally and the osteoblast surface ventrally. Finite element analysis of mechanical stress on the clivus revealed that compressive and tensile stresses appeared mainly on respective dorsal and ventral surfaces of the basioccipital bone. Osteoclastic bone resorption occurred primarily in the compression area, whereas areas of bone formation largely coincided with the tension area. These data collectively suggest that compressive and tensile stresses govern respective localization of osteoclasts and osteoblasts. Developmental analysis of the basioccipital bone revealed the clivus to be angled in early postnatal wild-type mice, whereas its slope was less prominent in Tnfsf11(−/−) mice, which lack osteoclasts. We propose that osteoclast-osteoblast “trans-pairing” across cortical bone is primarily induced by mechanical stress from growing organs and regulates shape and size of bones that encase the brain. Nature Publishing Group UK 2019-02-13 /pmc/articles/PMC6374512/ /pubmed/30760811 http://dx.doi.org/10.1038/s41598-018-38471-w Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Edamoto, Mio Kuroda, Yukiko Yoda, Masaki Kawaai, Katsuhiro Matsuo, Koichi Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development |
title | Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development |
title_full | Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development |
title_fullStr | Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development |
title_full_unstemmed | Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development |
title_short | Trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development |
title_sort | trans-pairing between osteoclasts and osteoblasts shapes the cranial base during development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374512/ https://www.ncbi.nlm.nih.gov/pubmed/30760811 http://dx.doi.org/10.1038/s41598-018-38471-w |
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