Bending and squeezing: gradual electric potentials encode mechanical stimuli in poplar.

IF 6.5 2区 生物学 Q1 PLANT SCIENCES
Erwan Tinturier, Éric Badel, Nathalie Leblanc-Fournier, Geoffroy Guéna, Yoël Forterre, Jean-Louis Julien
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Abstract

Mechanical stimuli such as wind elicit rapid electrical signals in plants, yet the mechanisms underlying 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 attenuation and propagation distance depend strongly on stimulus speed and intensity. While the maximal GP amplitude recorded near the bending site remained stable across stimulation conditions, slower or gentler flexions resulted in faster spatial decay and shorter propagation distances. Similar GP responses were elicited by stem bending and by direct root pressurization, indicating a coupling between hydraulic perturbations and electrical signaling. Although GP propagation and attenuation are consistent with a diffusive pressure signal, key features-such as the invariance of peak amplitude at the generation site and progressive waveform narrowing-cannot be explained by hydraulic diffusion alone and point to a nonlinear transduction process. Together, these results constrain the biophysical mechanisms underlying mechanically induced electrical signaling in trees and provide a framework for future studies addressing their physiological relevance.

杨树弯曲和挤压:渐进式电位编码机械刺激。
机械刺激如风在植物中引发快速的电信号,然而这些反应背后的机制仍然知之甚少。在此,我们研究了杨树幼树对控制茎秆弯曲的电生理反应。我们发现了一种不同于经典动作电位的渐进电位(GP),其衰减和传播距离与刺激速度和强度密切相关。虽然在弯曲部位附近记录的最大GP振幅在刺激条件下保持稳定,但较慢或较温和的弯曲导致更快的空间衰减和更短的传播距离。茎弯曲和直接根加压引起了类似的GP反应,表明水力扰动和电信号之间存在耦合。虽然GP的传播和衰减与扩散压力信号一致,但关键特征(如产生地点峰值振幅的不变性和波形的渐进变窄)不能单独用水力扩散来解释,并指向非线性转导过程。总之,这些结果限制了树木机械诱导电信号的生物物理机制,并为未来研究它们的生理相关性提供了框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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