Claudia Allan, Yiling Sun, Stephen C. Whisson, Michael Porter, Petra C. Boevink, Volker Nock and Claudia-Nicole Meisrimler
{"title":"利用双向双流根芯片观察根系生长和信号对胁迫梯度和病原体的反应","authors":"Claudia Allan, Yiling Sun, Stephen C. Whisson, Michael Porter, Petra C. Boevink, Volker Nock and Claudia-Nicole Meisrimler","doi":"10.1039/D4LC00659C","DOIUrl":null,"url":null,"abstract":"<p >Plants respond to environmental stressors with adaptive changes in growth and development. Central to these responses is the role of calcium (Ca<small><sup>2+</sup></small>) 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 <em>via</em> a multiplexed media delivery system (MMDS), dynamic gradients were created, mimicking natural environmental fluctuations. Signal analysis in <em>Arabidopsis thaliana</em> plants showed that the Ca<small><sup>2+</sup></small> burst indicated by the G-CaMP3 was concentration dependent. A Ca<small><sup>2+</sup></small> 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 <em>Phytophthora capsici</em> zoospores with <em>A. thaliana</em> roots was also studied. An immediate directional Ca<small><sup>2+</sup></small> signal was observed during early pathogen recognition, while a gradual, non-directional increase was observed in Orp1_roGFP fluorescent H<small><sub>2</sub></small>O<small><sub>2</sub></small> 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 <em>A. thaliana</em> and <em>Nicotiana benthamiana</em> roots when exposed to salinity induced by 100 mM NaCl, while <em>Solanum lycopersicum</em> 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.</p>","PeriodicalId":85,"journal":{"name":"Lab on a Chip","volume":" 24","pages":" 5360-5373"},"PeriodicalIF":6.1000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/lc/d4lc00659c?page=search","citationCount":"0","resultStr":"{\"title\":\"Observing root growth and signalling responses to stress gradients and pathogens using the bi-directional dual-flow RootChip†\",\"authors\":\"Claudia Allan, Yiling Sun, Stephen C. Whisson, Michael Porter, Petra C. Boevink, Volker Nock and Claudia-Nicole Meisrimler\",\"doi\":\"10.1039/D4LC00659C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Plants respond to environmental stressors with adaptive changes in growth and development. Central to these responses is the role of calcium (Ca<small><sup>2+</sup></small>) 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 <em>via</em> a multiplexed media delivery system (MMDS), dynamic gradients were created, mimicking natural environmental fluctuations. Signal analysis in <em>Arabidopsis thaliana</em> plants showed that the Ca<small><sup>2+</sup></small> burst indicated by the G-CaMP3 was concentration dependent. A Ca<small><sup>2+</sup></small> 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 <em>Phytophthora capsici</em> zoospores with <em>A. thaliana</em> roots was also studied. An immediate directional Ca<small><sup>2+</sup></small> signal was observed during early pathogen recognition, while a gradual, non-directional increase was observed in Orp1_roGFP fluorescent H<small><sub>2</sub></small>O<small><sub>2</sub></small> 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 <em>A. thaliana</em> and <em>Nicotiana benthamiana</em> roots when exposed to salinity induced by 100 mM NaCl, while <em>Solanum lycopersicum</em> exhibited growth increase over 90 minutes at the same NaCl concentration. 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Observing root growth and signalling responses to stress gradients and pathogens using the bi-directional dual-flow RootChip†
Plants respond to environmental stressors with adaptive changes in growth and development. Central to these responses is the role of calcium (Ca2+) 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 via a multiplexed media delivery system (MMDS), dynamic gradients were created, mimicking natural environmental fluctuations. Signal analysis in Arabidopsis thaliana plants showed that the Ca2+ burst indicated by the G-CaMP3 was concentration dependent. A Ca2+ 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 Phytophthora capsici zoospores with A. thaliana roots was also studied. An immediate directional Ca2+ signal was observed during early pathogen recognition, while a gradual, non-directional increase was observed in Orp1_roGFP fluorescent H2O2 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 A. thaliana and Nicotiana benthamiana roots when exposed to salinity induced by 100 mM NaCl, while Solanum lycopersicum 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.
期刊介绍:
Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.