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The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems

The epithelial-mesenchymal transition (EMT) is intrinsically linked to alterations of the intracellular cytoskeleton and the extracellular matrix. After EMT, cells acquire an elongated morphology with front/back polarity, which can be attributed to actin-driven protrusion formation as well as the ga...

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Autores principales: Leggett, Susan E., Hruska, Alex M., Guo, Ming, Wong, Ian Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7945251/
https://www.ncbi.nlm.nih.gov/pubmed/33691719
http://dx.doi.org/10.1186/s12964-021-00713-2
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author Leggett, Susan E.
Hruska, Alex M.
Guo, Ming
Wong, Ian Y.
author_facet Leggett, Susan E.
Hruska, Alex M.
Guo, Ming
Wong, Ian Y.
author_sort Leggett, Susan E.
collection PubMed
description The epithelial-mesenchymal transition (EMT) is intrinsically linked to alterations of the intracellular cytoskeleton and the extracellular matrix. After EMT, cells acquire an elongated morphology with front/back polarity, which can be attributed to actin-driven protrusion formation as well as the gain of vimentin expression. Consequently, cells can deform and remodel the surrounding matrix in order to facilitate local invasion. In this review, we highlight recent bioengineering approaches to elucidate EMT and functional changes in the cytoskeleton. First, we review transitions between multicellular clusters and dispersed individuals on planar surfaces, which often exhibit coordinated behaviors driven by leader cells and EMT. Second, we consider the functional role of vimentin, which can be probed at subcellular length scales and within confined spaces. Third, we discuss the role of topographical patterning and EMT via a contact guidance like mechanism. Finally, we address how multicellular clusters disorganize and disseminate in 3D matrix. These new technologies enable controlled physical microenvironments and higher-resolution spatiotemporal measurements of EMT at the single cell level. In closing, we consider future directions for the field and outstanding questions regarding EMT and the cytoskeleton for human cancer progression. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-021-00713-2.
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spelling pubmed-79452512021-03-10 The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems Leggett, Susan E. Hruska, Alex M. Guo, Ming Wong, Ian Y. Cell Commun Signal Review The epithelial-mesenchymal transition (EMT) is intrinsically linked to alterations of the intracellular cytoskeleton and the extracellular matrix. After EMT, cells acquire an elongated morphology with front/back polarity, which can be attributed to actin-driven protrusion formation as well as the gain of vimentin expression. Consequently, cells can deform and remodel the surrounding matrix in order to facilitate local invasion. In this review, we highlight recent bioengineering approaches to elucidate EMT and functional changes in the cytoskeleton. First, we review transitions between multicellular clusters and dispersed individuals on planar surfaces, which often exhibit coordinated behaviors driven by leader cells and EMT. Second, we consider the functional role of vimentin, which can be probed at subcellular length scales and within confined spaces. Third, we discuss the role of topographical patterning and EMT via a contact guidance like mechanism. Finally, we address how multicellular clusters disorganize and disseminate in 3D matrix. These new technologies enable controlled physical microenvironments and higher-resolution spatiotemporal measurements of EMT at the single cell level. In closing, we consider future directions for the field and outstanding questions regarding EMT and the cytoskeleton for human cancer progression. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-021-00713-2. BioMed Central 2021-03-10 /pmc/articles/PMC7945251/ /pubmed/33691719 http://dx.doi.org/10.1186/s12964-021-00713-2 Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Leggett, Susan E.
Hruska, Alex M.
Guo, Ming
Wong, Ian Y.
The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems
title The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems
title_full The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems
title_fullStr The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems
title_full_unstemmed The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems
title_short The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems
title_sort epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7945251/
https://www.ncbi.nlm.nih.gov/pubmed/33691719
http://dx.doi.org/10.1186/s12964-021-00713-2
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