Hydrogen Sulfide Increases Production of NADPH Oxidase-Dependent Hydrogen Peroxide and Phospholipase D-Derived Phosphatidic Acid in Guard Cell Signaling1
Hydrogen sulfide (H 2 S) is an important gaseous signaling molecule in plants that participates in stress responses and development. l -Cys desulfhydrase 1, one of the enzymatic sources of H 2 S in plants, participates in abscisic acid-induced stomatal closure. We combined pharmacological and geneti...
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Veröffentlicht in: | Plant physiology (Bethesda) 2018-02, Vol.176 (3), p.2532-2542 |
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Sprache: | eng |
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Zusammenfassung: | Hydrogen sulfide (H
2
S) is an important gaseous signaling molecule in plants that participates in stress responses and development.
l
-Cys desulfhydrase 1, one of the enzymatic sources of H
2
S in plants, participates in abscisic acid-induced stomatal closure. We combined pharmacological and genetic approaches to elucidate the involvement of H
2
S in stomatal closure and the interplay between H
2
S and other second messengers of the guard cell signaling network, such as hydrogen peroxide (H
2
O
2
) and phospholipase D (PLD)-derived phosphatidic acid in Arabidopsis (
Arabidopsis thaliana
). Both NADPH oxidase isoforms, respiratory burst oxidase homolog (RBOH)D and RBOHF, were required for H
2
S-induced stomatal closure. In vivo imaging using the cytosolic ratiometric fluorescent biosensor roGFP2-Orp1 revealed that H
2
S stimulates H
2
O
2
production in Arabidopsis guard cells. Additionally, we observed an interplay between H
2
S and PLD activity in the regulation of reactive oxygen species production and stomatal movement. The PLDα1 and PLDδ isoforms were required for H
2
S-induced stomatal closure, and most of the H
2
S-dependent H
2
O
2
production required the activity of PLDα1. Finally, we showed that H
2
S induced increases in the PLDδ-derived phosphatidic acid levels in guard cells. Our results revealed the involvement of H
2
S in the signaling network that controls stomatal closure, and suggest that H
2
S regulates NADPH oxidase and PLD activity in guard cells. |
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ISSN: | 0032-0889 1532-2548 |
DOI: | 10.1104/pp.17.01636 |