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Smithers, E. T.

Publications and source records attributed to Smithers, E. T..

2 recordsLinked to original sources

Cell Geometry and Junction Arrangement Define the Mechanical Robustness of Plant Tissues

Plant tissues are composed of immobile, pressurised cells that must maintain structural integrity under diverse environmental loads. Unlike animal tissues, which adapt through cellular rearrangement, plants must achieve mechanical robustness through the geometric configuration of their cellular networks. In this study, we establish a mechanistic link between cell geometry and mechanical resilience by integrating multilayer 3D mechanical simulations with cellular-resolution image analysis across a phylogenetically diverse panel of plant species, including Zea mays, Tradescantia zebrina, and Arabidopsis thaliana. We identify three-way junctions as fundamental mechanical elements that function as flexible hinges enabling mechanical strain accommodation in plant tissues. In contrast, four-way junctions are significantly stiffer and lack this strain-absorbing mechanism, providing a mechanical rationale for their biological avoidance. We also find that tissue material properties and strain response depend on edge lengths, cell layer, the degree of hexagonal shape, and turgor pressure response. These findings reveal the mechanism by which cell division patterns can actively tune tissue resilience to mechanical stress. This work provides new insights into the evolution of different cell shapes and offers clear principles for bio-inspired material science and tissue engineering.

plant biology↗

Mechanical stress orients stomata division to form tissue scale alignments.

The last stomatal division aligns with the leafs main axis in many species [1]. Understanding how cellular events such as these are coordinated across organ scales remains a challenge in developmental biology. In Arabidopsis, polarised proteins guide the asymmetric divisions in the early stomatal lineage. These proteins show organ scale alignment and may be sensitive to mechanical stress [2]. In contrast, what determines the orientation and alignment of the critical final division is unknown [3]. Here we use an artificial system where every cell adopts the fate of a stomata pore [4] making it easy to visualise their alignment. Combining this system with simultaneous time-lapse imaging on both sides of the cotyledon we are able to compare the stomatal orientation relative to the organ axis, the cell major axis, and the principal directions of growth. Using finite element modelling on a realistic template enabled us to identify differential growth-derived stress patterns as a factor coordinating stomata division at the organ scale. Mechanical perturbation confirmed the influence of tensile stress on stomata division orientation. Through this study, we have identified a mechanism that can explain this nearly century-old observation.

plant biology↗