Heavy metal toxicity: cadmium permeates through calcium channels and disturbs the plant water status

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<jats:title>Summary</jats:title><jats:p>Because plant wilting has been described as a consequence of cadmium (Cd<jats:sup>2+</jats:sup>) toxicity, we investigate Cd<jats:sup>2+</jats:sup> effects on plant water losses, gas exchanges and stomatal behaviour in <jats:italic>Arabidopsis thaliana</jats:italic> L. Effects of 1‐week Cd<jats:sup>2+</jats:sup> application in hydroponic condition (CdCl<jats:sub>2</jats:sub> 10–100 µ<jats:sc>m</jats:sc>) were analyzed. A 10‐µ<jats:sc>m</jats:sc> Cd<jats:sup>2+</jats:sup> concentration had no significant effect on the plant–water relationship and carbon assimilation. At higher Cd<jats:sup>2+</jats:sup> concentrations, a Cd<jats:sup>2+</jats:sup> ‐dependent decrease in leaf conductance and CO<jats:sub>2</jats:sub> uptake was observed despite the photosynthetic apparatus appeared not to be affected as probed by fluorescence measurements. In epidermal strip bioassays, nanomolar Cd<jats:sup>2+</jats:sup> concentrations reduced stomatal opening under light in <jats:italic>A. thaliana, Vicia faba</jats:italic> and <jats:italic>Commelina communis</jats:italic>. Application of 5 µ<jats:sc>m</jats:sc> ABA limited the root‐to‐shoot translocation of cadmium. However, the Cd<jats:sup>2+</jats:sup>‐induced stomatal closure was likely ABA‐independent, since a 5‐day treatment with 50 µ<jats:sc>m</jats:sc> Cd<jats:sup>2+</jats:sup> did not affect the plant relative water content. Additionally, a similar Cd<jats:sup>2+</jats:sup>‐induced stomatal closure was observed in the ABA insensitive mutant <jats:italic>abi1‐1</jats:italic>. Interestingly, this mutant displayed a higher transpiration rate than the wild type but did not accumulate more Cd<jats:sup>2+</jats:sup>, arguing that Cd<jats:sup>2+</jats:sup> uptake is not dependent only on the transpiration flow. Application of putative calcium channels inhibitors suppressed the inhibitory effect of Cd<jats:sup>2+</jats:sup> in epidermal strip experiments, suggesting that Cd<jats:sup>2+</jats:sup> could enter the guard cell through calcium channels. Patch‐clamp studies with <jats:italic>V. faba</jats:italic> guard cell protoplasts showed that plasma membrane K<jats:sup>+</jats:sup> channels were insensitive to external Cd<jats:sup>2+</jats:sup> application whereas Ca<jats:sup>2+</jats:sup> channels were found permeable to Cd<jats:sup>2+</jats:sup>. In conclusion, we propose that Cd<jats:sup>2+</jats:sup> affects guard cell regulation in an ABA‐independent manner by entering the cytosol via Ca<jats:sup>2+</jats:sup> channels.</jats:p>

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