2016
DOI: 10.1093/jxb/erw117
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Mapping nano-scale mechanical heterogeneity of primary plant cell walls

Abstract: HighlightMicromechanical maps on three plant systems universally reveal ‘soft’ and ‘hard’ domains on the cell wall surface; the observed micrometre-level spatial heterogeneity may be significant for cell growth and morphogenesis.

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Cited by 36 publications
(21 citation statements)
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“…The vertical confinement of the tubes eliminates the need for constant objective refocusing for long-term microscopy and the single directional and parallelized guidance allows for easier automation and post-processing of growth rates and other morphological assessment. Furthermore, the open channel architecture of the chip (Fig 1a) enables interfacing with well-established experimental platforms, such as the CFM and AFM for mechanical and surface morphology characterization of the cell wall [35,36], or to micro-injection systems for intra-cellular injection of dyes or internal turgor pressure measurement [23], as well as for chemical, electrical, thermal, or osmotic modification of the micro- or macro-environment around the growing pollen tube [3740]. The design easily allows for fluorescent dye loading via passive diffusion after germination [41] and by pressure shock in non-germinated pollen [42].…”
Section: Resultsmentioning
confidence: 99%
“…The vertical confinement of the tubes eliminates the need for constant objective refocusing for long-term microscopy and the single directional and parallelized guidance allows for easier automation and post-processing of growth rates and other morphological assessment. Furthermore, the open channel architecture of the chip (Fig 1a) enables interfacing with well-established experimental platforms, such as the CFM and AFM for mechanical and surface morphology characterization of the cell wall [35,36], or to micro-injection systems for intra-cellular injection of dyes or internal turgor pressure measurement [23], as well as for chemical, electrical, thermal, or osmotic modification of the micro- or macro-environment around the growing pollen tube [3740]. The design easily allows for fluorescent dye loading via passive diffusion after germination [41] and by pressure shock in non-germinated pollen [42].…”
Section: Resultsmentioning
confidence: 99%
“…More recently, quantitative force-volume mapping (QFM) was adapted to plant cell wall measurements utilizing continuous force curve recording and therefore solving the problem of heterogeneity observation by imaging the topography with the associated E and PI mappings. Studies on Arabidopsis thaliana reported different characteristic modes of deformation and a spatial distribution of the elastic moduli across the surface (Yakubov et al, 2016), while Radotic et al (2012) showed the changes in stiffness of the cell walls at different phases of growth. In addition, new innovative AFM techniques such as mode synthesized AFM (MSAFM) (Tetard et al, 2010(Tetard et al, , 2011 and hybrid photonic force microscopy (HPFM) (Tetard et al, 2015) have been FiGURe 1 | Chemical steps for delignification process starting from a cryotomed young poplar.…”
Section: Structurementioning
confidence: 99%
“…From skin to tree branches, many biological tissues exploit anisotropy and gradients in mechanical properties in order to achieve functionality [1][2][3][4]. In skin, the patterning of mechanical anisotropy allows the minimization of stresses when deformed through movement or the action of external forces [5].…”
Section: Introductionmentioning
confidence: 99%