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Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone

Strain magnitude has a controlling influence on bone adaptive response. However, questions remain as to how and if cancellous and cortical bone tissues respond differently to varied strain magnitudes, particularly at a molecular level. The goal of this study was to characterize the time‐dependent ge...

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Autores principales: Yang, Haisheng, Bullock, Whitney A, Myhal, Alexandra, DeShield, Philip, Duffy, Daniel, Main, Russell P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101616/
https://www.ncbi.nlm.nih.gov/pubmed/33977205
http://dx.doi.org/10.1002/jbm4.10489
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author Yang, Haisheng
Bullock, Whitney A
Myhal, Alexandra
DeShield, Philip
Duffy, Daniel
Main, Russell P
author_facet Yang, Haisheng
Bullock, Whitney A
Myhal, Alexandra
DeShield, Philip
Duffy, Daniel
Main, Russell P
author_sort Yang, Haisheng
collection PubMed
description Strain magnitude has a controlling influence on bone adaptive response. However, questions remain as to how and if cancellous and cortical bone tissues respond differently to varied strain magnitudes, particularly at a molecular level. The goal of this study was to characterize the time‐dependent gene expression, bone formation, and structural response of the cancellous and cortical bone of female C57Bl/6 mice to mechanical loading by applying varying load levels (low: −3.5 N; medium: −5.2 N; high: −7 N) to the skeleton using a mouse tibia loading model. The loading experiment showed that cortical bone mass at the tibial midshaft was significantly enhanced following all load levels examined and bone formation activities were particularly elevated at the medium and high loads applied. In contrast, for the proximal metaphyseal cancellous bone, only the high load led to significant increases in bone mass and bone formation indices. Similarly, expression of genes associated with inhibition of bone formation (e.g., Sost) was altered in the diaphyseal cortical bone at all load levels, but in the metaphyseal cortico‐cancellous bone only by the high load. Finite element analysis determined that the peak tensile or compressive strains that were osteogenic for the proximal cancellous bone under the high load were significantly greater than those that were osteogenic for the midshaft cortical tissues under the low load. These results suggest that the magnitude of the strain stimulus regulating structural, cellular, and molecular responses of bone to loading may be greater for the cancellous tissues than for the cortical tissues. © 2021 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
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spelling pubmed-81016162021-05-10 Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone Yang, Haisheng Bullock, Whitney A Myhal, Alexandra DeShield, Philip Duffy, Daniel Main, Russell P JBMR Plus Original Articles Strain magnitude has a controlling influence on bone adaptive response. However, questions remain as to how and if cancellous and cortical bone tissues respond differently to varied strain magnitudes, particularly at a molecular level. The goal of this study was to characterize the time‐dependent gene expression, bone formation, and structural response of the cancellous and cortical bone of female C57Bl/6 mice to mechanical loading by applying varying load levels (low: −3.5 N; medium: −5.2 N; high: −7 N) to the skeleton using a mouse tibia loading model. The loading experiment showed that cortical bone mass at the tibial midshaft was significantly enhanced following all load levels examined and bone formation activities were particularly elevated at the medium and high loads applied. In contrast, for the proximal metaphyseal cancellous bone, only the high load led to significant increases in bone mass and bone formation indices. Similarly, expression of genes associated with inhibition of bone formation (e.g., Sost) was altered in the diaphyseal cortical bone at all load levels, but in the metaphyseal cortico‐cancellous bone only by the high load. Finite element analysis determined that the peak tensile or compressive strains that were osteogenic for the proximal cancellous bone under the high load were significantly greater than those that were osteogenic for the midshaft cortical tissues under the low load. These results suggest that the magnitude of the strain stimulus regulating structural, cellular, and molecular responses of bone to loading may be greater for the cancellous tissues than for the cortical tissues. © 2021 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research. John Wiley & Sons, Inc. 2021-03-30 /pmc/articles/PMC8101616/ /pubmed/33977205 http://dx.doi.org/10.1002/jbm4.10489 Text en © 2021 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Yang, Haisheng
Bullock, Whitney A
Myhal, Alexandra
DeShield, Philip
Duffy, Daniel
Main, Russell P
Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone
title Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone
title_full Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone
title_fullStr Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone
title_full_unstemmed Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone
title_short Cancellous Bone May Have a Greater Adaptive Strain Threshold Than Cortical Bone
title_sort cancellous bone may have a greater adaptive strain threshold than cortical bone
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101616/
https://www.ncbi.nlm.nih.gov/pubmed/33977205
http://dx.doi.org/10.1002/jbm4.10489
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