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Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis

Architectured materials offer tailored mechanical properties but are limited in engineering applications due to challenges in maintaining toughness across their attachments. The enthesis connects tendon and bone, two vastly different architectured materials, and exhibits toughness across a wide rang...

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Autores principales: Golman, Mikhail, Abraham, Adam C., Kurtaliaj, Iden, Marshall, Brittany P., Hu, Yizhong Jenny, Schwartz, Andrea G., Guo, X. Edward, Birman, Victor, Thurner, Philipp J., Genin, Guy M., Thomopoulos, Stavros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626067/
https://www.ncbi.nlm.nih.gov/pubmed/34826240
http://dx.doi.org/10.1126/sciadv.abi5584
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author Golman, Mikhail
Abraham, Adam C.
Kurtaliaj, Iden
Marshall, Brittany P.
Hu, Yizhong Jenny
Schwartz, Andrea G.
Guo, X. Edward
Birman, Victor
Thurner, Philipp J.
Genin, Guy M.
Thomopoulos, Stavros
author_facet Golman, Mikhail
Abraham, Adam C.
Kurtaliaj, Iden
Marshall, Brittany P.
Hu, Yizhong Jenny
Schwartz, Andrea G.
Guo, X. Edward
Birman, Victor
Thurner, Philipp J.
Genin, Guy M.
Thomopoulos, Stavros
author_sort Golman, Mikhail
collection PubMed
description Architectured materials offer tailored mechanical properties but are limited in engineering applications due to challenges in maintaining toughness across their attachments. The enthesis connects tendon and bone, two vastly different architectured materials, and exhibits toughness across a wide range of loadings. Understanding the mechanisms by which this is achieved could inform the development of engineered attachments. Integrating experiments, simulations, and previously unexplored imaging that enabled simultaneous observation of mineralized and unmineralized tissues, we identified putative mechanisms of enthesis toughening in a mouse model and then manipulated these mechanisms via in vivo control of mineralization and architecture. Imaging uncovered a fibrous architecture within the enthesis that controls trade-offs between strength and toughness. In vivo models of pathology revealed architectural adaptations that optimize these trade-offs through cross-scale mechanisms including nanoscale protein denaturation, milliscale load-sharing, and macroscale energy absorption. Results suggest strategies for optimizing architecture for tough bimaterial attachments in medicine and engineering.
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spelling pubmed-86260672021-12-06 Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis Golman, Mikhail Abraham, Adam C. Kurtaliaj, Iden Marshall, Brittany P. Hu, Yizhong Jenny Schwartz, Andrea G. Guo, X. Edward Birman, Victor Thurner, Philipp J. Genin, Guy M. Thomopoulos, Stavros Sci Adv Biomedicine and Life Sciences Architectured materials offer tailored mechanical properties but are limited in engineering applications due to challenges in maintaining toughness across their attachments. The enthesis connects tendon and bone, two vastly different architectured materials, and exhibits toughness across a wide range of loadings. Understanding the mechanisms by which this is achieved could inform the development of engineered attachments. Integrating experiments, simulations, and previously unexplored imaging that enabled simultaneous observation of mineralized and unmineralized tissues, we identified putative mechanisms of enthesis toughening in a mouse model and then manipulated these mechanisms via in vivo control of mineralization and architecture. Imaging uncovered a fibrous architecture within the enthesis that controls trade-offs between strength and toughness. In vivo models of pathology revealed architectural adaptations that optimize these trade-offs through cross-scale mechanisms including nanoscale protein denaturation, milliscale load-sharing, and macroscale energy absorption. Results suggest strategies for optimizing architecture for tough bimaterial attachments in medicine and engineering. American Association for the Advancement of Science 2021-11-26 /pmc/articles/PMC8626067/ /pubmed/34826240 http://dx.doi.org/10.1126/sciadv.abi5584 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Golman, Mikhail
Abraham, Adam C.
Kurtaliaj, Iden
Marshall, Brittany P.
Hu, Yizhong Jenny
Schwartz, Andrea G.
Guo, X. Edward
Birman, Victor
Thurner, Philipp J.
Genin, Guy M.
Thomopoulos, Stavros
Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis
title Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis
title_full Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis
title_fullStr Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis
title_full_unstemmed Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis
title_short Toughening mechanisms for the attachment of architectured materials: The mechanics of the tendon enthesis
title_sort toughening mechanisms for the attachment of architectured materials: the mechanics of the tendon enthesis
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626067/
https://www.ncbi.nlm.nih.gov/pubmed/34826240
http://dx.doi.org/10.1126/sciadv.abi5584
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