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Characterization of the Developing Lacunocanalicular Network During Fracture Repair

Fracture repair is a normal physiological response to bone injury. During the process of bony callus formation, a lacunocanalicular network (LCN) is formed de novo that evolves with callus remodeling. Our aim was the longitudinal assessment of the development and evolution of the LCN during fracture...

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Autores principales: Casanova, Michele, Schindeler, Aaron, Peacock, Lauren, Lee, Lucinda, Schneider, Philipp, Little, David G., Müller, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441443/
https://www.ncbi.nlm.nih.gov/pubmed/34532613
http://dx.doi.org/10.1002/jbm4.10525
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author Casanova, Michele
Schindeler, Aaron
Peacock, Lauren
Lee, Lucinda
Schneider, Philipp
Little, David G.
Müller, Ralph
author_facet Casanova, Michele
Schindeler, Aaron
Peacock, Lauren
Lee, Lucinda
Schneider, Philipp
Little, David G.
Müller, Ralph
author_sort Casanova, Michele
collection PubMed
description Fracture repair is a normal physiological response to bone injury. During the process of bony callus formation, a lacunocanalicular network (LCN) is formed de novo that evolves with callus remodeling. Our aim was the longitudinal assessment of the development and evolution of the LCN during fracture repair. To this end, 45 adult wild‐type C57BL/6 mice underwent closed tibial fracture surgery. Fractured and intact contralateral tibias were harvested after 2, 3, and 6 weeks of bone healing (n = 15/group). High‐resolution micro–computed tomography (μCT) and deconvolution microscopy (DV) approaches were applied to quantify lacunar number density from the calluses and intact bone. On histological sections, Goldner's trichrome staining was used to assess lacunar occupancy, fluorescein isothiocyanate staining to visualize the canalicular network, and terminal deoxynucleotidyl transferase–mediated deoxyuridine triphosphate‐biotin nick end labeling (TUNEL) staining to examine osteocyte apoptosis. Analysis of μCT scans showed progressive decreases in mean lacuna volume over time (−27% 2–3 weeks; −13% 3–6 weeks). Lacunar number density increased considerably between 2 and 3 weeks (+156%). Correlation analysis was performed, showing a positive linear relationship between canalicular number density and trabecular thickness (R (2) = 0.56, p < 0.001) and an inverse relationship between mean lacuna volume and trabecular thickness (R (2) = 0.57, p < 0.001). Histology showed increases in canalicular number density over time (+22% 2–3 weeks, +51% 3–6 weeks). Lacunar occupancy in new bone of the callus was high (>90%), but the old cortical bone within the fracture site appeared necrotic as it underwent resorption. In conclusion, our data shows a progressive increase in the complexity of the LCN over time during fracture healing and demonstrates that this network is initiated during the early stages of repair. Further studies are needed to address the functional importance of osteocytes in bone healing, particularly in detecting and translating the effects of micromotion in the fracture. © 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-84414432021-09-15 Characterization of the Developing Lacunocanalicular Network During Fracture Repair Casanova, Michele Schindeler, Aaron Peacock, Lauren Lee, Lucinda Schneider, Philipp Little, David G. Müller, Ralph JBMR Plus Original Articles Fracture repair is a normal physiological response to bone injury. During the process of bony callus formation, a lacunocanalicular network (LCN) is formed de novo that evolves with callus remodeling. Our aim was the longitudinal assessment of the development and evolution of the LCN during fracture repair. To this end, 45 adult wild‐type C57BL/6 mice underwent closed tibial fracture surgery. Fractured and intact contralateral tibias were harvested after 2, 3, and 6 weeks of bone healing (n = 15/group). High‐resolution micro–computed tomography (μCT) and deconvolution microscopy (DV) approaches were applied to quantify lacunar number density from the calluses and intact bone. On histological sections, Goldner's trichrome staining was used to assess lacunar occupancy, fluorescein isothiocyanate staining to visualize the canalicular network, and terminal deoxynucleotidyl transferase–mediated deoxyuridine triphosphate‐biotin nick end labeling (TUNEL) staining to examine osteocyte apoptosis. Analysis of μCT scans showed progressive decreases in mean lacuna volume over time (−27% 2–3 weeks; −13% 3–6 weeks). Lacunar number density increased considerably between 2 and 3 weeks (+156%). Correlation analysis was performed, showing a positive linear relationship between canalicular number density and trabecular thickness (R (2) = 0.56, p < 0.001) and an inverse relationship between mean lacuna volume and trabecular thickness (R (2) = 0.57, p < 0.001). Histology showed increases in canalicular number density over time (+22% 2–3 weeks, +51% 3–6 weeks). Lacunar occupancy in new bone of the callus was high (>90%), but the old cortical bone within the fracture site appeared necrotic as it underwent resorption. In conclusion, our data shows a progressive increase in the complexity of the LCN over time during fracture healing and demonstrates that this network is initiated during the early stages of repair. Further studies are needed to address the functional importance of osteocytes in bone healing, particularly in detecting and translating the effects of micromotion in the fracture. © 2021 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research. John Wiley & Sons, Inc. 2021-07-12 /pmc/articles/PMC8441443/ /pubmed/34532613 http://dx.doi.org/10.1002/jbm4.10525 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
Casanova, Michele
Schindeler, Aaron
Peacock, Lauren
Lee, Lucinda
Schneider, Philipp
Little, David G.
Müller, Ralph
Characterization of the Developing Lacunocanalicular Network During Fracture Repair
title Characterization of the Developing Lacunocanalicular Network During Fracture Repair
title_full Characterization of the Developing Lacunocanalicular Network During Fracture Repair
title_fullStr Characterization of the Developing Lacunocanalicular Network During Fracture Repair
title_full_unstemmed Characterization of the Developing Lacunocanalicular Network During Fracture Repair
title_short Characterization of the Developing Lacunocanalicular Network During Fracture Repair
title_sort characterization of the developing lacunocanalicular network during fracture repair
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441443/
https://www.ncbi.nlm.nih.gov/pubmed/34532613
http://dx.doi.org/10.1002/jbm4.10525
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