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Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface

The enthesis allows the insertion of tendon into bone thanks to several remarkable strategies. This complex and clinically relevant location often features a thin layer of fibrocartilage sandwiched between tendon and bone to cope with a highly heterogeneous mechanical environment. The main purpose o...

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Autores principales: Tits, Alexandra, Plougonven, Erwan, Blouin, Stéphane, Hartmann, Markus A., Kaux, Jean-François, Drion, Pierre, Fernandez, Justin, van Lenthe, G. Harry, Ruffoni, Davide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367976/
https://www.ncbi.nlm.nih.gov/pubmed/34400706
http://dx.doi.org/10.1038/s41598-021-95917-4
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author Tits, Alexandra
Plougonven, Erwan
Blouin, Stéphane
Hartmann, Markus A.
Kaux, Jean-François
Drion, Pierre
Fernandez, Justin
van Lenthe, G. Harry
Ruffoni, Davide
author_facet Tits, Alexandra
Plougonven, Erwan
Blouin, Stéphane
Hartmann, Markus A.
Kaux, Jean-François
Drion, Pierre
Fernandez, Justin
van Lenthe, G. Harry
Ruffoni, Davide
author_sort Tits, Alexandra
collection PubMed
description The enthesis allows the insertion of tendon into bone thanks to several remarkable strategies. This complex and clinically relevant location often features a thin layer of fibrocartilage sandwiched between tendon and bone to cope with a highly heterogeneous mechanical environment. The main purpose of this study was to investigate whether mineralized fibrocartilage and bone close to the enthesis show distinctive three-dimensional microstructural features, possibly to enable load transfer from tendon to bone. As a model, the Achilles tendon-calcaneus bone system of adult rats was investigated with histology, backscattered electron imaging and micro-computed tomography. The microstructural porosity of bone and mineralized fibrocartilage in different locations including enthesis fibrocartilage, periosteal fibrocartilage and bone away from the enthesis was characterized. We showed that calcaneus bone presents a dedicated protrusion of low porosity where the tendon inserts. A spatially resolved analysis of the trabecular network suggests that such protrusion may promote force flow from the tendon to the plantar ligament, while partially relieving the trabecular bone from such a task. Focusing on the tuberosity, highly specific microstructural aspects were highlighted. Firstly, the interface between mineralized and unmineralized fibrocartilage showed the highest roughness at the tuberosity, possibly to increase failure resistance of a region carrying large stresses. Secondly, fibrochondrocyte lacunae inside mineralized fibrocartilage, in analogy with osteocyte lacunae in bone, had a predominant alignment at the enthesis and a rather random organization away from it. Finally, the network of subchondral channels inside the tuberosity was highly anisotropic when compared to contiguous regions. This dual anisotropy of subchondral channels and cell lacunae at the insertion may reflect the alignment of the underlying collagen network. Our findings suggest that the microstructure of fibrocartilage may be linked with the loading environment. Future studies should characterize those microstructural aspects in aged and or diseased conditions to elucidate the poorly understood role of bone and fibrocartilage in enthesis-related pathologies.
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spelling pubmed-83679762021-08-17 Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface Tits, Alexandra Plougonven, Erwan Blouin, Stéphane Hartmann, Markus A. Kaux, Jean-François Drion, Pierre Fernandez, Justin van Lenthe, G. Harry Ruffoni, Davide Sci Rep Article The enthesis allows the insertion of tendon into bone thanks to several remarkable strategies. This complex and clinically relevant location often features a thin layer of fibrocartilage sandwiched between tendon and bone to cope with a highly heterogeneous mechanical environment. The main purpose of this study was to investigate whether mineralized fibrocartilage and bone close to the enthesis show distinctive three-dimensional microstructural features, possibly to enable load transfer from tendon to bone. As a model, the Achilles tendon-calcaneus bone system of adult rats was investigated with histology, backscattered electron imaging and micro-computed tomography. The microstructural porosity of bone and mineralized fibrocartilage in different locations including enthesis fibrocartilage, periosteal fibrocartilage and bone away from the enthesis was characterized. We showed that calcaneus bone presents a dedicated protrusion of low porosity where the tendon inserts. A spatially resolved analysis of the trabecular network suggests that such protrusion may promote force flow from the tendon to the plantar ligament, while partially relieving the trabecular bone from such a task. Focusing on the tuberosity, highly specific microstructural aspects were highlighted. Firstly, the interface between mineralized and unmineralized fibrocartilage showed the highest roughness at the tuberosity, possibly to increase failure resistance of a region carrying large stresses. Secondly, fibrochondrocyte lacunae inside mineralized fibrocartilage, in analogy with osteocyte lacunae in bone, had a predominant alignment at the enthesis and a rather random organization away from it. Finally, the network of subchondral channels inside the tuberosity was highly anisotropic when compared to contiguous regions. This dual anisotropy of subchondral channels and cell lacunae at the insertion may reflect the alignment of the underlying collagen network. Our findings suggest that the microstructure of fibrocartilage may be linked with the loading environment. Future studies should characterize those microstructural aspects in aged and or diseased conditions to elucidate the poorly understood role of bone and fibrocartilage in enthesis-related pathologies. Nature Publishing Group UK 2021-08-16 /pmc/articles/PMC8367976/ /pubmed/34400706 http://dx.doi.org/10.1038/s41598-021-95917-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tits, Alexandra
Plougonven, Erwan
Blouin, Stéphane
Hartmann, Markus A.
Kaux, Jean-François
Drion, Pierre
Fernandez, Justin
van Lenthe, G. Harry
Ruffoni, Davide
Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface
title Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface
title_full Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface
title_fullStr Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface
title_full_unstemmed Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface
title_short Local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface
title_sort local anisotropy in mineralized fibrocartilage and subchondral bone beneath the tendon-bone interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367976/
https://www.ncbi.nlm.nih.gov/pubmed/34400706
http://dx.doi.org/10.1038/s41598-021-95917-4
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