Allan Claudia, Sun Yiling, Whisson Stephen C, Porter Michael, Boevink Petra C, Nock Volker, Meisrimler Claudia-Nicole
School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch, New Zealand.
MacDiarmid Institute for Advanced Materials and Nanotechnology, PO Box 600, Wellington 6140, New Zealand.
Lab Chip. 2024 Dec 3;24(24):5360-5373. doi: 10.1039/d4lc00659c.
Plants respond to environmental stressors with adaptive changes in growth and development. Central to these responses is the role of calcium (Ca) as a key secondary messenger. Here, the bi-directional dual-flow RootChip (bi-dfRC) microfluidic platform was used to study defence signalling and root growth. By introducing salinity as sodium chloride (NaCl) treatment a multiplexed media delivery system (MMDS), dynamic gradients were created, mimicking natural environmental fluctuations. Signal analysis in plants showed that the Ca burst indicated by the G-CaMP3 was concentration dependent. A Ca burst initiated in response to salinity increase, specifically within the stele tissue, for 30 seconds. The signal then intensified in epidermal cells directly in contact with the stressor, spreading directionally towards the root tip, over 5 minutes. Inhibition of propidium iodide (PI) stain transport through the xylem was observed following salinity increase, contrasting with flow observed under control conditions. The interaction of zoospores with roots was also studied. An immediate directional Ca signal was observed during early pathogen recognition, while a gradual, non-directional increase was observed in Orp1_roGFP fluorescent HO levels, over 30 min. By adjusting the dimensions of the bi-dfRC, plants with varying root architectures were subjected to growth analysis. Growth reduction was observed in and roots when exposed to salinity induced by 100 mM NaCl, while exhibited growth increase over 90 minutes at the same NaCl concentration. Furthermore, novel insights into force sensing in roots were gained through the engineering of displaceable pillars into the bi-dfRC channel. These findings highlight the vital role of controlling fluid flow in microfluidic channels in advancing our understanding of root physiology under stress conditions.
植物通过生长和发育的适应性变化来应对环境压力源。这些反应的核心是钙(Ca)作为关键的第二信使的作用。在这里,双向双流根芯片(bi-dfRC)微流控平台被用于研究防御信号传导和根系生长。通过引入氯化钠(NaCl)处理作为盐度,构建了一个多路复用介质输送系统(MMDS),创建了动态梯度,模拟自然环境波动。对植物的信号分析表明,由G-CaMP3指示的钙爆发是浓度依赖性的。盐度增加时会引发钙爆发,特别是在中柱组织内,持续30秒。然后信号在直接与压力源接触的表皮细胞中增强,并在5分钟内朝着根尖方向扩散。盐度增加后,观察到碘化丙啶(PI)染色通过木质部的运输受到抑制,这与对照条件下观察到的流动情况形成对比。还研究了游动孢子与根的相互作用。在早期病原体识别过程中观察到即时的定向钙信号,而在30分钟内,Orp1_roGFP荧光HO水平观察到逐渐的、非定向的增加。通过调整bi-dfRC的尺寸,对具有不同根系结构的植物进行了生长分析。当暴露于100 mM NaCl诱导的盐度时,和根的生长受到抑制,而在相同NaCl浓度下,在90分钟内表现出生长增加。此外,通过在bi-dfRC通道中设计可移动支柱,获得了关于根中力感知的新见解。这些发现突出了控制微流控通道中流体流动在推进我们对胁迫条件下根系生理学理解方面的重要作用。