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Leblanc-Fournier, N.

Publications and source records attributed to Leblanc-Fournier, N..

5 recordsLinked to original sources

Bending and Squeezing: Gradual Potentials Encode Mechanical Stimuli in Poplar

Mechanical stimuli such as wind elicit rapid electrical signals in plants, yet the mechanisms driving these responses remain poorly understood. Here, we investigated the electrophysiological responses of young poplar trees to controlled stem bending. We identified a gradual potential (GP) distinct from classical action potentials, whose amplitude attenuation and propagation distance were strongly influenced by stimulus speed and intensity. Although maximal GP amplitude near the bending site remained stable across stimulation setups, slower and gentler flexions led to more rapid spatial decay and reduced signal propagation. Similar GP responses were observed following either stem bending or direct root pressurization, suggesting hydraulic-electrical coupling. These results suggest that mechanical stress induces a transient hydraulic pressure wave that triggers the GP. While the GPs attenuation and propagation dynamics resemble those of a diffusive pressure signal, key features--such as constant peak amplitude regardless of stimulus strength and progressive signal narrowing--point to a complex, non-linear transduction mechanism. Altogether, our findings reveal a finely tuned system where spatial and temporal dynamics of this non-action potential electrical signal encode detailed information about mechanical stimuli, potentially allowing plants to adaptively respond to fluctuating environmental forces like wind. HighlightRoot pressurization generates electrical signals similar to stem bending in poplar, suggesting hydroelectric coupling in plant mechanosensing and wind intensity encoding.

plant biology↗

Temporal modification of H3K9/14ac and H3K4me3 histone marks mediates mechano-responsive gene expression during the accommodation process in poplar.

Plants can attenuate their molecular response to repetitive mechanical stimulation as a function of their mechanical history. For instance, a single bending of stem is sufficient to attenuate the gene expression in poplar plants to the subsequent mechanical stimulation, and the state of desensitization can last for several days. The role of histone modifications in memory gene expression and modulating plant response to abiotic or biotic signals is well known. However, such information is still lacking to explain the attenuated expression pattern of mechano-responsive genes in plants under repetitive stimulation. Using poplar as a model plant in this study, we first measured the global level of H3K9/14ac and H3K4me3 marks in the bent stem. The result shows that a single mild bending of the stem for 6 seconds is sufficient to alter the global level of the H3K9/14ac mark in poplar, highlighting the fact that plants are extremely sensitive to mechanical signals. Next, we analyzed the temporal dynamics of these two active histone marks at attenuated (PtaZFP2, PtaXET6, and PtaACA13) and non-attenuated (PtaHRD) mechano-responsive loci during the desensitization and resensitization phases. Enrichment of H3K9/14ac and H3K4me3 in the regulatory region of attenuated genes correlates well with their transient expression pattern after the first bending. Moreover, the levels of H3K4me3 correlate well with their expression pattern after the second bending at desensitization (3 days after the first bending) as well as resensitization (5 days after the first bending) phases. On the other hand, H3K9/14ac status correlates only with their attenuated expression pattern at the desensitization phase. The expression efficiency of the attenuated genes was restored after the second bending in the histone deacetylase inhibitor-treated plants. While both histone modifications contribute to the expression of attenuated genes, mechanostimulated expression of the non-attenuated PtaHRD gene seems to be H3K4me3 dependent.

plant biology↗

Pathogen-derived mechanical cues regulate the spatio-temporal implementation of plant defense

How immune responses are activated and regulated is a central question in immunology. In addition to molecular signaling, recent work has shown that physical forces regulate the immune response of vertebrates by modifying transmembrane protein conformation and cell contact. Mechanical stress and strain produced by forces constitute physical cues perceived by cells instructing gene expression. Whether mechanical cues generated by pathogens during host colonization can trigger adaptive responses in plant cells remains elusive. We found that local and progressive variations of plant cell wall tension caused by fungal pathogen attacks are transmitted to neighboring healthy tissue around the infection site and trigger immunity in distal cells. This thigmoimmunity process requires the reorganization of cortical microtubules and contributes strongly to Arabidopsis disease resistance. One-Sentence SummaryActivation of plants immunity depends on fluctuations of mechanical tension caused by a fungal pathogen.

plant biology↗

Stem bending generates electrical response in poplar

Under natural conditions, plants experience external mechanical stresses such as wind and touch that impact their growth. A remarkable feature of this mechanically induced growth response is that it may occur at distance from the stimulation site, suggesting the existence of a signal propagating through the plant. In this study, we investigated the electrical response of poplar trees to a transient controlled bending stimulation of the stem that mimics the mechanical effect of wind. Stem bending was found to cause an electrical response that we called gradual potential, similar in shape to an action potential. However, this signal distinguished from the well-known plant action potential by its propagation up to 20 cm along the stem and its strong dumping in velocity and amplitude. Two hypotheses regarding the mode of propagation of the gradual potential are discussed. One sentence summaryPoplar stem bending induces an electrical response with high speed and strong decrement.

plant biology↗

Transduction of mechanical cellular oscillation by the plasma-membrane mechanosensitive channel MSL10

Throughout their life, plants are submitted to recurrent cyclic mechanical loading due to wind. The resulting passive oscillation movements of stem and foliage is an important phenomenon for biological and ecological issues such as photosynthesis optimization 1-3 and thermal exchange 4. The induced motions at plant scale are well described and analyzed, with oscillations at typically 1 to 3 Hz in trees 5-10. However, the cellular perception and transduction of such recurring mechanical signals remains an open question. Multimeric protein complexes forming mechanosensitive (MS) channels embedded in the membrane provide an efficient system to rapidly convert mechanical tension into electrical signal 11. Here we show that the plasma membrane mechanosensitive channel MscS-LIKE 10 (MSL10) from the model plant Arabidopsis thaliana responds to pulsed membrane stretching with rapid activation and relaxation kinetics in the range of one second. Under sinusoidal membrane stretching MSL10 presents a greater activity than under static stimulation and behaves as a large bandpass oscillation \"follower\" without filtering the signal in the range of 0.3 to 3 Hz. With a localization in aerial organs naturally submitted to oscillations, our results suggest that the mechanosensitive channel MSL10 represents a molecular component of a universal system of oscillatory perception in plants.

plant biology↗