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Rear traction forces drive adherent tissue migration in vivo

During animal embryogenesis, homeostasis and disease, tissues push and pull on their surroundings to move forward. Although the force-generating machinery is known, it is unknown how tissues exert physical stresses on their substrate to generate motion in vivo. Here, we identify the force transmissi...

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Autores principales: Yamaguchi, Naoya, Zhang, Ziyi, Schneider, Teseo, Wang, Biran, Panozzo, Daniele, Knaut, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868490/
https://www.ncbi.nlm.nih.gov/pubmed/35165417
http://dx.doi.org/10.1038/s41556-022-00844-9
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author Yamaguchi, Naoya
Zhang, Ziyi
Schneider, Teseo
Wang, Biran
Panozzo, Daniele
Knaut, Holger
author_facet Yamaguchi, Naoya
Zhang, Ziyi
Schneider, Teseo
Wang, Biran
Panozzo, Daniele
Knaut, Holger
author_sort Yamaguchi, Naoya
collection PubMed
description During animal embryogenesis, homeostasis and disease, tissues push and pull on their surroundings to move forward. Although the force-generating machinery is known, it is unknown how tissues exert physical stresses on their substrate to generate motion in vivo. Here, we identify the force transmission machinery, the substrate, and the stresses that a tissue, the zebrafish posterior lateral line primordium, generates during its migration. We find that the primordium couples actin flow through integrins to the basement membrane for forward movement. Talin/integrin-mediated coupling is required for efficient migration, and its loss is partly compensated for by increased actin flow. Using Embryogram, an approach to measure stresses in vivo, we show that the primordium’s rear exerts higher stresses than the front, suggesting that this tissue pushes itself forward with its back. This unexpected strategy likely also underlies the motion of other tissues in animals.
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spelling pubmed-88684902022-08-14 Rear traction forces drive adherent tissue migration in vivo Yamaguchi, Naoya Zhang, Ziyi Schneider, Teseo Wang, Biran Panozzo, Daniele Knaut, Holger Nat Cell Biol Article During animal embryogenesis, homeostasis and disease, tissues push and pull on their surroundings to move forward. Although the force-generating machinery is known, it is unknown how tissues exert physical stresses on their substrate to generate motion in vivo. Here, we identify the force transmission machinery, the substrate, and the stresses that a tissue, the zebrafish posterior lateral line primordium, generates during its migration. We find that the primordium couples actin flow through integrins to the basement membrane for forward movement. Talin/integrin-mediated coupling is required for efficient migration, and its loss is partly compensated for by increased actin flow. Using Embryogram, an approach to measure stresses in vivo, we show that the primordium’s rear exerts higher stresses than the front, suggesting that this tissue pushes itself forward with its back. This unexpected strategy likely also underlies the motion of other tissues in animals. 2022-02 2022-02-14 /pmc/articles/PMC8868490/ /pubmed/35165417 http://dx.doi.org/10.1038/s41556-022-00844-9 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms
spellingShingle Article
Yamaguchi, Naoya
Zhang, Ziyi
Schneider, Teseo
Wang, Biran
Panozzo, Daniele
Knaut, Holger
Rear traction forces drive adherent tissue migration in vivo
title Rear traction forces drive adherent tissue migration in vivo
title_full Rear traction forces drive adherent tissue migration in vivo
title_fullStr Rear traction forces drive adherent tissue migration in vivo
title_full_unstemmed Rear traction forces drive adherent tissue migration in vivo
title_short Rear traction forces drive adherent tissue migration in vivo
title_sort rear traction forces drive adherent tissue migration in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868490/
https://www.ncbi.nlm.nih.gov/pubmed/35165417
http://dx.doi.org/10.1038/s41556-022-00844-9
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