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Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure
Humanized mouse models are increasingly studied to recapitulate human-like bone physiology. While human and mouse bone architectures differ in multiple scales, the extent to which chimeric human-mouse bone physiologically interacts and structurally integrates remains unknown. Here, we identify that...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608795/ https://www.ncbi.nlm.nih.gov/pubmed/33115741 http://dx.doi.org/10.1126/sciadv.abb9265 |
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author | Moreno-Jiménez, I. Cipitria, A. Sánchez-Herrero, A. van Tol, A. F. Roschger, A. Lahr, C. A. McGovern, J. A. Hutmacher, D. W. Fratzl, P. |
author_facet | Moreno-Jiménez, I. Cipitria, A. Sánchez-Herrero, A. van Tol, A. F. Roschger, A. Lahr, C. A. McGovern, J. A. Hutmacher, D. W. Fratzl, P. |
author_sort | Moreno-Jiménez, I. |
collection | PubMed |
description | Humanized mouse models are increasingly studied to recapitulate human-like bone physiology. While human and mouse bone architectures differ in multiple scales, the extent to which chimeric human-mouse bone physiologically interacts and structurally integrates remains unknown. Here, we identify that humanized bone is formed by a mosaic of human and mouse collagen, structurally integrated within the same bone organ, as shown by immunohistochemistry. Combining this with materials science techniques, we investigate the extracellular matrix of specific human and mouse collagen regions. We show that human-like osteocyte lacunar-canalicular network is retained within human collagen regions and is distinct to that of mouse tissue. This multiscale analysis shows that human and mouse tissues physiologically integrate into a single, functional bone tissue while maintaining their species-specific ultrastructural differences. These results offer an original method to validate and advance tissue-engineered human-like bone in chimeric animal models, which grow to be eloquent tools in biomedical research. |
format | Online Article Text |
id | pubmed-7608795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76087952020-11-13 Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure Moreno-Jiménez, I. Cipitria, A. Sánchez-Herrero, A. van Tol, A. F. Roschger, A. Lahr, C. A. McGovern, J. A. Hutmacher, D. W. Fratzl, P. Sci Adv Research Articles Humanized mouse models are increasingly studied to recapitulate human-like bone physiology. While human and mouse bone architectures differ in multiple scales, the extent to which chimeric human-mouse bone physiologically interacts and structurally integrates remains unknown. Here, we identify that humanized bone is formed by a mosaic of human and mouse collagen, structurally integrated within the same bone organ, as shown by immunohistochemistry. Combining this with materials science techniques, we investigate the extracellular matrix of specific human and mouse collagen regions. We show that human-like osteocyte lacunar-canalicular network is retained within human collagen regions and is distinct to that of mouse tissue. This multiscale analysis shows that human and mouse tissues physiologically integrate into a single, functional bone tissue while maintaining their species-specific ultrastructural differences. These results offer an original method to validate and advance tissue-engineered human-like bone in chimeric animal models, which grow to be eloquent tools in biomedical research. American Association for the Advancement of Science 2020-10-28 /pmc/articles/PMC7608795/ /pubmed/33115741 http://dx.doi.org/10.1126/sciadv.abb9265 Text en Copyright © 2020 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/ 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 | Research Articles Moreno-Jiménez, I. Cipitria, A. Sánchez-Herrero, A. van Tol, A. F. Roschger, A. Lahr, C. A. McGovern, J. A. Hutmacher, D. W. Fratzl, P. Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure |
title | Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure |
title_full | Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure |
title_fullStr | Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure |
title_full_unstemmed | Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure |
title_short | Human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure |
title_sort | human and mouse bones physiologically integrate in a humanized mouse model while maintaining species-specific ultrastructure |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608795/ https://www.ncbi.nlm.nih.gov/pubmed/33115741 http://dx.doi.org/10.1126/sciadv.abb9265 |
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