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Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells

Cellular forces, mechanics and other physical factors are important co-regulators of normal cell and tissue physiology. These cues are often misregulated in diseases such as cancer, where altered tissue mechanics contribute to the disease progression. Furthermore, intercellular tensile and compressi...

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Autores principales: Mäntylä, Elina, Ihalainen, Teemu O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445989/
https://www.ncbi.nlm.nih.gov/pubmed/34531455
http://dx.doi.org/10.1038/s41598-021-97900-5
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author Mäntylä, Elina
Ihalainen, Teemu O.
author_facet Mäntylä, Elina
Ihalainen, Teemu O.
author_sort Mäntylä, Elina
collection PubMed
description Cellular forces, mechanics and other physical factors are important co-regulators of normal cell and tissue physiology. These cues are often misregulated in diseases such as cancer, where altered tissue mechanics contribute to the disease progression. Furthermore, intercellular tensile and compressive force-related signaling is highlighted in collective cell behavior during development. However, the mechanistic understanding on the role of physical forces in regulation of cellular physiology, including gene expression and signaling, is still lacking. This is partly because studies on the molecular mechanisms of force transmission require easily controllable experimental designs. These approaches should enable both easy mechanical manipulation of cells and, importantly, readouts ranging from microscopy imaging to biochemical assays. To achieve a robust solution for mechanical manipulation of cells, we developed devices built of LEGO bricks allowing manual, motorized and/or cyclic cell stretching and compression studies. By using these devices, we show that [Formula: see text] -catenin responds differentially to epithelial monolayer stretching and lateral compression, either localizing more to the cell nuclei or cell–cell junctions, respectively. In addition, we show that epithelial compression drives cytoplasmic retention and phosphorylation of transcription coregulator YAP1. We provide a complete part listing and video assembly instructions, allowing other researchers to build and use the devices in cellular mechanics-related studies.
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spelling pubmed-84459892021-09-20 Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells Mäntylä, Elina Ihalainen, Teemu O. Sci Rep Article Cellular forces, mechanics and other physical factors are important co-regulators of normal cell and tissue physiology. These cues are often misregulated in diseases such as cancer, where altered tissue mechanics contribute to the disease progression. Furthermore, intercellular tensile and compressive force-related signaling is highlighted in collective cell behavior during development. However, the mechanistic understanding on the role of physical forces in regulation of cellular physiology, including gene expression and signaling, is still lacking. This is partly because studies on the molecular mechanisms of force transmission require easily controllable experimental designs. These approaches should enable both easy mechanical manipulation of cells and, importantly, readouts ranging from microscopy imaging to biochemical assays. To achieve a robust solution for mechanical manipulation of cells, we developed devices built of LEGO bricks allowing manual, motorized and/or cyclic cell stretching and compression studies. By using these devices, we show that [Formula: see text] -catenin responds differentially to epithelial monolayer stretching and lateral compression, either localizing more to the cell nuclei or cell–cell junctions, respectively. In addition, we show that epithelial compression drives cytoplasmic retention and phosphorylation of transcription coregulator YAP1. We provide a complete part listing and video assembly instructions, allowing other researchers to build and use the devices in cellular mechanics-related studies. Nature Publishing Group UK 2021-09-16 /pmc/articles/PMC8445989/ /pubmed/34531455 http://dx.doi.org/10.1038/s41598-021-97900-5 Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mäntylä, Elina
Ihalainen, Teemu O.
Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells
title Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells
title_full Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells
title_fullStr Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells
title_full_unstemmed Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells
title_short Brick Strex: a robust device built of LEGO bricks for mechanical manipulation of cells
title_sort brick strex: a robust device built of lego bricks for mechanical manipulation of cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445989/
https://www.ncbi.nlm.nih.gov/pubmed/34531455
http://dx.doi.org/10.1038/s41598-021-97900-5
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