Biology subjects

Durand-Smet, P.

Publications and source records attributed to Durand-Smet, P..

5 recordsLinked to original sources

bioRxiv2025

Spatiotemporal Analysis Reveals Mechanisms Controlling Reactive Oxygen Species and Calcium Interplay Following Root Compression

Mechanical stimulation of the root triggers signal transduction involving Reactive Oxygen Species (ROS) and calcium, but their relationships are unclear. This study aims to clarify the temporal and spatial interrelations between calcium and ROS following a localized lateral compression of the root. We combined a microfluidic valve rootchip to apply controlled compression, with fluorescent probes and wide-field or confocal microscopy to monitor H2O2 and calcium dynamics in root tissues simultaneously. Pharmacological inhibitors were used to investigate the causal links between H2O2 and calcium responses. In response to compression, we observed transient H2O2 accumulation, with characteristics similar to the calcium response observed previously in the same microfluidic system. H2O2 and calcium response occurred in 3 kinetic phases: a fast calcium increase relying on mechanosensitive channels and external calcium entry, followed by a long-lasting H2O2 accumulation and a slow calcium increase depending on NADPH oxidase activity. H2O2 accumulated in all root tissues while calcium increases were confined to the root center. These results suggest that two mechanotransduction mechanisms are involved in root response to compression. One mechanism relies on plasma membrane mechanosensitive channels, triggering a fast calcium increase. Another independent mechanism, relying on FERONIA, induces H2O2 accumulation, which drives the slower secondary calcium increase.

plant biology↗

bioRxiv2025

Single Root hair growth under constant force: insights into wall mechanics

Tip growth is a tightly regulated process that enables root hairs to explore their surroundings, enhancing plant development, particularly by improving nutrient uptake. While Lockharts viscoplastic framework is widely used to describe this process, it has received limited experimental validation. By integrating optical microscopy with a custom microplate-based rheometer, we created a novel protocol to simultaneously measure, for individual growing root hairs, both the reduction in growth rate and the instantaneous compression in response to a step in applied axial force. The observed growth rate reduction aligns remarkably with a 1D Lockhart viscoplastic model, experimentally validating this framework in tip-growing cells. Additionally, the instantaneous compression upon force application provided an in situ estimate of turgor pressure. Together, these measurements allowed us to determine, for the first time in Arabidopsis root hairs, two critical parameters: the yield turgor pressure and cell wall viscosity. Our approach--including the technique, protocol, and analytical framework--can be readily adapted to other tip-growing species and diverse experimental conditions (e.g., varying nutrient availability or osmotic stress). This opens new opportunities to explore cell wall mechanosensitivity and its role in adapting tip growth to environmental signals. Significance StatementPlant growth relies on their ability to anchor roots in soil and maximize nutrient uptake. This process partly depends on root hairs. These long tubular extensions develop from the root surface, exhibiting a highly directional growth process --tip growth. Understanding how root hair growth adapts to soil mechanics is crucial, especially with climate change and soil hardening. We present a novel, non-invasive technique to probe the mechanics of root hair walls--key to their growth. By applying a feedback-controlled force, we can investigate the effect of mechanical resistance on root hair growth while preventing buckling, thus accessing elusive cell wall features. This method holds broader significance, as tip-driven growth is also used by fungi and yeasts to colonize their environments.

biophysics↗

bioRxiv2025

Synthetic pectin-cellulose nanofiber capsule provides minimal model capturing mechanics of a regenerating plant cell wall

Plant primary cell walls are dynamic supramolecular assemblies composed of layered cellulose, hemicellulose and pectin, progressively built through synthesis and secretion. However, the specific architectural features and structural components sufficient to endow the mechanical properties of the wall remain unclear. Here, we construct a minimal synthetic spherical shell and compare its structural and mechanical properties to those of a plant single-cell system. To eliminate complexities from intercellular connectivity and developmental history, we exploit the ability of plant protoplasts to regenerate cell walls de novo. Compression tests of regenerating protoplasts between parallel plates reveal that wall stiffness increases with wall thickening over time. Despite differences in assembly pathways, architecture, and composition, the synthetic shell exhibits a similar thickness-dependent modulus and similar material stiffness. The synthetic shell, composed of pectin and cellulose layers, mirrors the mechanical behavior of regenerating primary cell walls, suggesting that these components are sufficient to confer key viscoelastic properties in the limit of small deformations. Given the complexity of natural plant cell walls, the synthetic analogue offers a controllable platform to dissect the mechanical contributions of individual wall components.

plant biology↗

bioRxiv2025

Allometric spreading and focal adhesion collective organization are coordinated by cell-scale geometrical constraints

Focal adhesions are protein complexes that transmit actin cytoskeleton forces to the extracellular matrix and serve as signaling hubs that regulate cell physiology. While their growth is achieved through a local force-dependent process, the requirement of sustaining stress at the cell scale suggests a global regulation of the collective organization of focal adhesions. To investigate evidence of such large-scale regulation, we compared changes in cell shape and the organization of focal adhesion-like structures during the early spreading of fibroblasts either on a two-dimensional substrate or confined between two parallel plates, and for cells of different volumes. In this way, we reveal that the areal density of focal adhesions is conserved regardless of cell size or third-dimensional confinement, despite different absolute values of the surface covered by adhesion clusters. In particular, the width of the focal adhesions ring, which fills the flat lamella at the cell front, adapts to cell size and third-dimensional confinement and scales with cell-substrate contact radius. We find that this contact radius also adapts in the parallel-plate geometry so that the cumulated area of cellsubstrate contact is conserved at the cell scale. We suggest that this behavior is the result of 3D cell shape changes which govern spreading transitions. Indeed, because of volume conservation constraints, the evolution of cell-body contact angle adjusts according to cell size and confinement, whereas the rate of early spreading at the cell-substrate contact is not affected by thirddimensional geometry. Overall, our data suggest that a coordination between global and local scales mediates the adaptation of cell-substrate contacts and focal adhesions distribution to large scale geometrical constraints, which allows an invariant cell-substrate adhesive energy.

biophysics↗

bioRxiv2019

Cytoskeletal organization in isolated plant cells under geometry control.

Specific cell and tissue form is essential to support many biological functions of living organisms. During development, the creation of different shapes at the cellular and tissue level fundamentally requires the integration of genetic, biochemical and physical inputs.\n\nIt is well established that the cortical microtubule network plays a key role in the morphogenesis of the plant cell wall by guiding the organisation of new cell wall material. Moreover, it has been suggested that light or mechanical stresses can orient the microtubules thereby controlling wall architecture and plant cell shape. The cytoskeleton is thus a major determinant of plant cell shape. What is less clear is how cell shape in turn influences cytoskeletal organization.\n\nRecent in vitro experiments and numerical simulations predicted that a geometry-based rule is sufficient to explain some of the microtubule organization observed in cells. Due to their high flexural rigidity and persistence length of the order of a few millimeters, MTs are rigid over cellular dimensions and are thus expected to align along their long axis if constrained in specific geometries. This hypothesis remains to be tested in cellulo.\n\nHere we present an experimental approach to explore the relative contribution of geometry to the final organization of actin and microtubule cytoskeletons in single plant cells. We show that, in cells constrained in rectangular shapes, the cytoskeleton align along the long axis of the cells. By studying actin and microtubules in cells with the same system we show that while actin organisation requires microtubules to be present to align the converse is not the case. A model of self organizing microtubules in 3D predicts that severing of microtubules is an important parameter controlling the anisotropy of the microtubule network. We experimentally confirmed the model predictions by analysing the response to shape change in plant cells with altered microtubule severing dynamics. This work is a first step towards assessing quantitatively how cell geometry contributes to the control of cytoskeletal organization in living plant cells.

biophysics↗