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Article

Structure and Biomechanics during Xylem Vessel Transdifferentiation in Arabidopsis thaliana

1
Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195, USA
2
Division of Engineering and Applied Science, California Institute of Technology, Pasadena, CA 91125, USA
3
Biological Imaging Facility, California Institute of Technology, Pasadena, CA 91125, USA
4
Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa 277-8562, Japan
5
Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma 630-0192, Japan
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Plants 2020, 9(12), 1715; https://doi.org/10.3390/plants9121715
Received: 27 October 2020 / Revised: 30 November 2020 / Accepted: 3 December 2020 / Published: 5 December 2020
(This article belongs to the Special Issue Mechanical Signaling in Plants)
Individual plant cells are the building blocks for all plantae and artificially constructed plant biomaterials, like biocomposites. Secondary cell walls (SCWs) are a key component for mediating mechanical strength and stiffness in both living vascular plants and biocomposite materials. In this paper, we study the structure and biomechanics of cultured plant cells during the cellular developmental stages associated with SCW formation. We use a model culture system that induces transdifferentiation of Arabidopsis thaliana cells to xylem vessel elements, upon treatment with dexamethasone (DEX). We group the transdifferentiation process into three distinct stages, based on morphological observations of the cell walls. The first stage includes cells with only a primary cell wall (PCW), the second covers cells that have formed a SCW, and the third stage includes cells with a ruptured tonoplast and partially or fully degraded PCW. We adopt a multi-scale approach to study the mechanical properties of cells in these three stages. We perform large-scale indentations with a micro-compression system in three different osmotic conditions. Atomic force microscopy (AFM) nanoscale indentations in water allow us to isolate the cell wall response. We propose a spring-based model to deconvolve the competing stiffness contributions from turgor pressure, PCW, SCW and cytoplasm in the stiffness of differentiating cells. Prior to triggering differentiation, cells in hypotonic pressure conditions are significantly stiffer than cells in isotonic or hypertonic conditions, highlighting the dominant role of turgor pressure. Plasmolyzed cells with a SCW reach similar levels of stiffness as cells with maximum turgor pressure. The stiffness of the PCW in all of these conditions is lower than the stiffness of the fully-formed SCW. Our results provide the first experimental characterization of the mechanics of SCW formation at single cell level. View Full-Text
Keywords: plant biomechanics; turgor pressure; micro-compression; AFM; Arabidopsis thaliana; differentiation plant biomechanics; turgor pressure; micro-compression; AFM; Arabidopsis thaliana; differentiation
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MDPI and ACS Style

Roumeli, E.; Ginsberg, L.; McDonald, R.; Spigolon, G.; Hendrickx, R.; Ohtani, M.; Demura, T.; Ravichandran, G.; Daraio, C. Structure and Biomechanics during Xylem Vessel Transdifferentiation in Arabidopsis thaliana. Plants 2020, 9, 1715. https://doi.org/10.3390/plants9121715

AMA Style

Roumeli E, Ginsberg L, McDonald R, Spigolon G, Hendrickx R, Ohtani M, Demura T, Ravichandran G, Daraio C. Structure and Biomechanics during Xylem Vessel Transdifferentiation in Arabidopsis thaliana. Plants. 2020; 9(12):1715. https://doi.org/10.3390/plants9121715

Chicago/Turabian Style

Roumeli, Eleftheria, Leah Ginsberg, Robin McDonald, Giada Spigolon, Rodinde Hendrickx, Misato Ohtani, Taku Demura, Guruswami Ravichandran, and Chiara Daraio. 2020. "Structure and Biomechanics during Xylem Vessel Transdifferentiation in Arabidopsis thaliana" Plants 9, no. 12: 1715. https://doi.org/10.3390/plants9121715

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