Unverified paper record
Hypoxia-activated fluorescent probes as markers of oxygen levels in plant cells and tissues
bioRxiv · 25 Feb 2025 · 10.1101/2025.02.20.639250
Abstract
O_LILow oxygen signalling in plants is important in development and stress responses. Measurement of oxygen levels in plant cells and tissues is hampered by a lack of chemical tools with which to reliably detect and quantify endogenous oxygen availability. We have exploited hypoxia-activated fluorescent probes to visualise low oxygen (hypoxia) in plant cells and tissues. C_LIO_LIWe applied 4-nitrobenzyl (4NB-) resorufin and methyl-indolequinone (MeIQ-) resorufin to Arabidopsis thaliana whole cells and seedlings exposed to hypoxia (1% O2) and normoxia (21% O2). Confocal microscopy and fluorescence intensity measurements were used to visualise regions of resorufin fluorescence. C_LIO_LIBoth probes enter A.thaliana whole cells and are activated to fluoresce selectively in hypoxic conditions. Similarly, incubation with A.thaliana seedlings resulted in hypoxia-dependent activation of both probes and observation of fluorescence in hypoxic roots and leaf tissue. MeIQ-Resorufin was used to visualise endogenous hypoxia in lateral root primordia of normoxic A.thaliana seedlings. C_LIO_LIOxygen measurement in plants until now has relied on invasive probes or genetic manipulation. Use of these chemical probes to detect applied and endogenous hypoxia has the potential to facilitate a greater understanding of oxygen dynamics in plant cells and tissues, allowing correlation of oxygen concentrations with adaptive and developmental responses to hypoxia. C_LI
Plant phenotyping relevance
植物細胞・組織の低酸素状態を蛍光プローブで可視化・測定する化学的フェノタイピング手法の開発と検証が中心であり、単なる生物学的応用ではない。
abstractWe have exploited hypoxia-activated fluorescent probes to visualise low oxygen (hypoxia) in plant cells and tissues.
abstractConfocal microscopy and fluorescence intensity measurements were used to visualise regions of resorufin fluorescence.
abstractBoth probes enter A.thaliana whole cells and are activated to fluoresce selectively in hypoxic conditions.
Code and data availability
The supplied blocks describe probe synthesis, plant growth, hypoxia treatments, confocal imaging, and ImageJ/Prism/R analyses, but contain no public phenotype dataset, image deposit, author analysis code, or data availability statement with a URL. No paper-specific public asset is identified.
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