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Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds
Many essential cellular processes are regulated by mechanical properties of their microenvironment. Here, we introduce stimuli-responsive composite scaffolds fabricated by three-dimensional (3D) laser lithography to simultaneously stretch large numbers of single cells in tailored 3D microenvironment...
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/PMC7531888/ https://www.ncbi.nlm.nih.gov/pubmed/32967835 http://dx.doi.org/10.1126/sciadv.abc2648 |
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author | Hippler, Marc Weißenbruch, Kai Richler, Kai Lemma, Enrico D. Nakahata, Masaki Richter, Benjamin Barner-Kowollik, Christopher Takashima, Yoshinori Harada, Akira Blasco, Eva Wegener, Martin Tanaka, Motomu Bastmeyer, Martin |
author_facet | Hippler, Marc Weißenbruch, Kai Richler, Kai Lemma, Enrico D. Nakahata, Masaki Richter, Benjamin Barner-Kowollik, Christopher Takashima, Yoshinori Harada, Akira Blasco, Eva Wegener, Martin Tanaka, Motomu Bastmeyer, Martin |
author_sort | Hippler, Marc |
collection | PubMed |
description | Many essential cellular processes are regulated by mechanical properties of their microenvironment. Here, we introduce stimuli-responsive composite scaffolds fabricated by three-dimensional (3D) laser lithography to simultaneously stretch large numbers of single cells in tailored 3D microenvironments. The key material is a stimuli-responsive photoresist containing cross-links formed by noncovalent, directional interactions between β-cyclodextrin (host) and adamantane (guest). This allows reversible actuation under physiological conditions by application of soluble competitive guests. Cells adhering in these scaffolds build up initial traction forces of ~80 nN. After application of an equibiaxial stretch of up to 25%, cells remodel their actin cytoskeleton, double their traction forces, and equilibrate at a new dynamic set point within 30 min. When the stretch is released, traction forces gradually decrease until the initial set point is retrieved. Pharmacological inhibition or knockout of nonmuscle myosin 2A prevents these adjustments, suggesting that cellular tensional homeostasis strongly depends on functional myosin motors. |
format | Online Article Text |
id | pubmed-7531888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75318882020-10-13 Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds Hippler, Marc Weißenbruch, Kai Richler, Kai Lemma, Enrico D. Nakahata, Masaki Richter, Benjamin Barner-Kowollik, Christopher Takashima, Yoshinori Harada, Akira Blasco, Eva Wegener, Martin Tanaka, Motomu Bastmeyer, Martin Sci Adv Research Articles Many essential cellular processes are regulated by mechanical properties of their microenvironment. Here, we introduce stimuli-responsive composite scaffolds fabricated by three-dimensional (3D) laser lithography to simultaneously stretch large numbers of single cells in tailored 3D microenvironments. The key material is a stimuli-responsive photoresist containing cross-links formed by noncovalent, directional interactions between β-cyclodextrin (host) and adamantane (guest). This allows reversible actuation under physiological conditions by application of soluble competitive guests. Cells adhering in these scaffolds build up initial traction forces of ~80 nN. After application of an equibiaxial stretch of up to 25%, cells remodel their actin cytoskeleton, double their traction forces, and equilibrate at a new dynamic set point within 30 min. When the stretch is released, traction forces gradually decrease until the initial set point is retrieved. Pharmacological inhibition or knockout of nonmuscle myosin 2A prevents these adjustments, suggesting that cellular tensional homeostasis strongly depends on functional myosin motors. American Association for the Advancement of Science 2020-09-23 /pmc/articles/PMC7531888/ /pubmed/32967835 http://dx.doi.org/10.1126/sciadv.abc2648 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 Hippler, Marc Weißenbruch, Kai Richler, Kai Lemma, Enrico D. Nakahata, Masaki Richter, Benjamin Barner-Kowollik, Christopher Takashima, Yoshinori Harada, Akira Blasco, Eva Wegener, Martin Tanaka, Motomu Bastmeyer, Martin Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds |
title | Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds |
title_full | Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds |
title_fullStr | Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds |
title_full_unstemmed | Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds |
title_short | Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds |
title_sort | mechanical stimulation of single cells by reversible host-guest interactions in 3d microscaffolds |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531888/ https://www.ncbi.nlm.nih.gov/pubmed/32967835 http://dx.doi.org/10.1126/sciadv.abc2648 |
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