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Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes

Mechanical patterns control a variety of biological processes in plants. The microviscosity of cellular structures effects the diffusion rate of molecules and organelles, thereby affecting processes such as metabolism and signaling. Spatial variations in local viscosity are also generated during fun...

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Autores principales: Michels, Lucile, Gorelova, Vera, Harnvanichvech, Yosapol, Borst, Jan Willem, Albada, Bauke, Weijers, Dolf, Sprakel, Joris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395454/
https://www.ncbi.nlm.nih.gov/pubmed/32669427
http://dx.doi.org/10.1073/pnas.1921374117
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author Michels, Lucile
Gorelova, Vera
Harnvanichvech, Yosapol
Borst, Jan Willem
Albada, Bauke
Weijers, Dolf
Sprakel, Joris
author_facet Michels, Lucile
Gorelova, Vera
Harnvanichvech, Yosapol
Borst, Jan Willem
Albada, Bauke
Weijers, Dolf
Sprakel, Joris
author_sort Michels, Lucile
collection PubMed
description Mechanical patterns control a variety of biological processes in plants. The microviscosity of cellular structures effects the diffusion rate of molecules and organelles, thereby affecting processes such as metabolism and signaling. Spatial variations in local viscosity are also generated during fundamental events in the cell life cycle. While crucial to a complete understanding of plant mechanobiology, resolving subcellular microviscosity patterns in plants has remained an unsolved challenge. We present an imaging microviscosimetry toolbox of molecular rotors that yield complete microviscosity maps of cells and tissues, specifically targeting the cytosol, vacuole, plasma membrane, and wall of plant cells. These boron-dipyrromethene (BODIPY)-based molecular rotors are rigidochromic by means of coupling the rate of an intramolecular rotation, which depends on the mechanics of their direct surroundings, with their fluorescence lifetime. This enables the optical mapping of fluidity and porosity patterns in targeted cellular compartments. We show how apparent viscosity relates to cell function in the root, how the growth of cellular protrusions induces local tension, and how the cell wall is adapted to perform actuation surrounding leaf pores. These results pave the way to the noninvasive micromechanical mapping of complex tissues.
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spelling pubmed-73954542020-08-07 Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes Michels, Lucile Gorelova, Vera Harnvanichvech, Yosapol Borst, Jan Willem Albada, Bauke Weijers, Dolf Sprakel, Joris Proc Natl Acad Sci U S A Biological Sciences Mechanical patterns control a variety of biological processes in plants. The microviscosity of cellular structures effects the diffusion rate of molecules and organelles, thereby affecting processes such as metabolism and signaling. Spatial variations in local viscosity are also generated during fundamental events in the cell life cycle. While crucial to a complete understanding of plant mechanobiology, resolving subcellular microviscosity patterns in plants has remained an unsolved challenge. We present an imaging microviscosimetry toolbox of molecular rotors that yield complete microviscosity maps of cells and tissues, specifically targeting the cytosol, vacuole, plasma membrane, and wall of plant cells. These boron-dipyrromethene (BODIPY)-based molecular rotors are rigidochromic by means of coupling the rate of an intramolecular rotation, which depends on the mechanics of their direct surroundings, with their fluorescence lifetime. This enables the optical mapping of fluidity and porosity patterns in targeted cellular compartments. We show how apparent viscosity relates to cell function in the root, how the growth of cellular protrusions induces local tension, and how the cell wall is adapted to perform actuation surrounding leaf pores. These results pave the way to the noninvasive micromechanical mapping of complex tissues. National Academy of Sciences 2020-07-28 2020-07-15 /pmc/articles/PMC7395454/ /pubmed/32669427 http://dx.doi.org/10.1073/pnas.1921374117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Michels, Lucile
Gorelova, Vera
Harnvanichvech, Yosapol
Borst, Jan Willem
Albada, Bauke
Weijers, Dolf
Sprakel, Joris
Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes
title Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes
title_full Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes
title_fullStr Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes
title_full_unstemmed Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes
title_short Complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes
title_sort complete microviscosity maps of living plant cells and tissues with a toolbox of targeting mechanoprobes
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395454/
https://www.ncbi.nlm.nih.gov/pubmed/32669427
http://dx.doi.org/10.1073/pnas.1921374117
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