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Abstract Mechanical properties, size and geometry of cells, and internal turgor pressure greatly influence cell morphogenesis. Computational models of cell growth require values for wall elastic modulus and turgor pressure, but very few experiments have been designed to validate the results using measurements that deform the entire thickness of the cell wall. New wall material is synthesized at the inner surface of the cell such that full-thickness deformations are needed to quantify relevant changes associated with cell development. Here, we present an integrated, experimental–computational approach to analyze quantitatively the variation of elastic bending behavior in the primary cell wall of living Arabidopsis (Arabidopsis thaliana) pavement cells and to measure turgor pressure within cells under different osmotic conditions. This approach used laser scanning confocal microscopy to measure the 3D geometry of single pavement cells and indentation experiments to probe the local mechanical responses across the periclinal wall. The experimental results were matched iteratively using a finite element model of the experiment to determine the local mechanical properties and turgor pressure. The resulting modulus distribution along the periclinal wall was nonuniform across the leaf cells studied. These results were consistent with the characteristics of plant cell walls which have a heterogeneous organization. The results and model allowed the magnitude and orientation of cell wall stress to be predicted quantitatively. The methods also serve as a reference for future work to analyze the morphogenetic behaviors of plant cells in terms of the heterogeneity and anisotropy of cell walls.
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This content will become publicly available on September 3, 2026
Developmental changes in epidermal anatomy, drought tolerance, and biomechanics in the leaves of a tropical fern
Throughout leaf development, cell expansion is dynamic and driven by the balance between local cell wall mechanical properties and the intracellular turgor pressure that overcomes the stiffness of the cell wall leading to plastic deformation. The epidermal pavement cells in most leaves begin development as small, polygonally shaped cells, but in mature leaves epidermal pavement cells are often shaped as highly lobed puzzle pieces. However, the developmental and biomechanical trajectories between these two end points have not before been fully characterized. Here we characterized how epidermal pavement cell size and shape, cell wall thickness, and hydraulic traits change during leaf expansion in the tropical understory fern Microsorum grossum (Polypodiaceae). As fronds expanded by approximately two orders of magnitude in size, epidermal pavement cells became increasingly lobed as cell walls thickened. Furthermore, the timing of these developmental changes varied across the lamina, start first near the frond base and midrib, followed by more apical and lateral regions. During expansion, fronds also underwent substantial physiological changes: as cells expanded and cell walls thickened, intracellular turgor pressure and the bulk cell wall modulus of elasticity both increased while the water potential at turgor loss and the minimum epidermal conductance to water vapor both decreased. These results highlight the dynamic coordination between anatomical and physiological traits throughout leaf development, provide valuable data for biophysical modeling of leaf development, and highlight the vulnerability of developing leaves to drought conditions.
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- PAR ID:
- 10636073
- Publisher / Repository:
- Oxford University Press
- Date Published:
- Journal Name:
- Annals of Botany
- ISSN:
- 0305-7364
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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