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Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation
Classic microsurgical techniques, such as those used in the early 1900s by Mangold and Spemann, have been instrumental in advancing our understanding of embryonic development. However, these techniques are highly specialized, leading to issues of inter-operator variability. Here we introduce a user-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789989/ https://www.ncbi.nlm.nih.gov/pubmed/36566327 http://dx.doi.org/10.1038/s41467-022-35632-4 |
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author | Özelçi, Ece Mailand, Erik Rüegg, Matthias Oates, Andrew C. Sakar, Mahmut Selman |
author_facet | Özelçi, Ece Mailand, Erik Rüegg, Matthias Oates, Andrew C. Sakar, Mahmut Selman |
author_sort | Özelçi, Ece |
collection | PubMed |
description | Classic microsurgical techniques, such as those used in the early 1900s by Mangold and Spemann, have been instrumental in advancing our understanding of embryonic development. However, these techniques are highly specialized, leading to issues of inter-operator variability. Here we introduce a user-friendly robotic microsurgery platform that allows precise mechanical manipulation of soft tissues in zebrafish embryos. Using our platform, we reproducibly targeted precise regions of tail explants, and quantified the response in real-time by following notochord and presomitic mesoderm (PSM) morphogenesis and segmentation clock dynamics during vertebrate anteroposterior axis elongation. We find an extension force generated through the posterior notochord that is strong enough to buckle the structure. Our data suggest that this force generates a unidirectional notochord extension towards the tailbud because PSM tissue around the posterior notochord does not let it slide anteriorly. These results complement existing biomechanical models of axis elongation, revealing a critical coupling between the posterior notochord, the tailbud, and the PSM, and show that somite patterning is robust against structural perturbations. |
format | Online Article Text |
id | pubmed-9789989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97899892022-12-26 Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation Özelçi, Ece Mailand, Erik Rüegg, Matthias Oates, Andrew C. Sakar, Mahmut Selman Nat Commun Article Classic microsurgical techniques, such as those used in the early 1900s by Mangold and Spemann, have been instrumental in advancing our understanding of embryonic development. However, these techniques are highly specialized, leading to issues of inter-operator variability. Here we introduce a user-friendly robotic microsurgery platform that allows precise mechanical manipulation of soft tissues in zebrafish embryos. Using our platform, we reproducibly targeted precise regions of tail explants, and quantified the response in real-time by following notochord and presomitic mesoderm (PSM) morphogenesis and segmentation clock dynamics during vertebrate anteroposterior axis elongation. We find an extension force generated through the posterior notochord that is strong enough to buckle the structure. Our data suggest that this force generates a unidirectional notochord extension towards the tailbud because PSM tissue around the posterior notochord does not let it slide anteriorly. These results complement existing biomechanical models of axis elongation, revealing a critical coupling between the posterior notochord, the tailbud, and the PSM, and show that somite patterning is robust against structural perturbations. Nature Publishing Group UK 2022-12-24 /pmc/articles/PMC9789989/ /pubmed/36566327 http://dx.doi.org/10.1038/s41467-022-35632-4 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Özelçi, Ece Mailand, Erik Rüegg, Matthias Oates, Andrew C. Sakar, Mahmut Selman Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation |
title | Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation |
title_full | Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation |
title_fullStr | Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation |
title_full_unstemmed | Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation |
title_short | Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation |
title_sort | deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789989/ https://www.ncbi.nlm.nih.gov/pubmed/36566327 http://dx.doi.org/10.1038/s41467-022-35632-4 |
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