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Yaaran, A.

Publications and source records attributed to Yaaran, A..

6 recordsLinked to original sources

Disentangling the stomatal response to transpiration and relative humidity

Stomatal responses to atmospheric conditions are critical for balancing plant CO2 gain with water loss. Yet, the question of whether stomata respond directly to humidity or to the rate of water loss (transpiration) remains unresolved due to the tight coupling between these variables. To decouple them, we manipulated water vapor diffusivity using Helox (21% O2, 79% He), where vapor diffuses 2.33 times faster than in air, and Argox (21% O2, 79% Ar), where it diffuses 0.75 times slower. This allows control of VPD and transpiration independent of one another while maintaining a constant leaf temperature. We investigated the stomatal conductance (gsw) responses to air and Helox in several plant species, including Solanum lycopersicum, Vitis vinifera, and the fern Nephrolepis exaltata. In addition, we tested the Commelina communis, with coupled gas exchange and real-time imaging of stomatal aperture in intact leaves. In all angiosperms tested, we observed that stomatal closing was triggered exclusively by reductions in RH rather than by transpiration increases. When transpiration increased, but relative humidity remained constant, we detected an increase in gsw without a following decrease in the experimental time span. Exposure to Argox without altering RH reduced transpiration, likely enabling restoration of epidermal turgor and inducing passive mechanical closure. However, the rate of stomatal closure under reduced RH was 2.35 times faster than that observed under Argox, suggesting that passive turgor-driven responses cannot fully explain the kinetics or extent of closure under dry air. This work provides direct experimental evidence for humidity-driven stomatal closure.

plant biology↗

A tale of two pumps: Blue light and ABA alter Arabidopsis leaf hydraulics via bundle sheath cells H+-pumps and channels

This study focuses on the cellular mechanism underlying the co-regulation of the leaf hydraulic conductance (Kleaf) by blue light (BL) and the stress hormone ABA in Arabidopsis thaliana. Our previous work has demonstrated that (1) Kleaf increased by BL signaling within the leaf bundle sheath cells (BSCs), which activated their plasmalemma (PM) H+-ATPase (AHA2), acidifying the xylem sap; (2) external acidification enhanced the BSCs Kleaf and their osmotic water permeability (Pf); (3) ABA decreased both Kleaf and Pf by reducing the BSCs PM aquaporins activity. We now show, using pH and EM (membrane potential) probes combined with H+-pumps inhibitors and manipulations of cytosolic and external Ca2+ concentrations ([Ca2+]CYT, [Ca2+]EXT, respectively), that, in the BSCs: (a) under BL, ABA inhibits AHA2, depolarizing the BSCs and alkalinizing the xylem sap, (b) ABA stimulates the BSCs vacuolar H+-ATPase (VHA), alkalinizing their cytosol; (c) each pump stimulation, AHA2 by BL and VHA by ABA, requires [Ca2+]CYT elevation. ABA-effect-mimicking conditions in patch-clamp experiments activate the BSCs K+-release channels (SKOR and/or GORK). ABA decreased the Kleaf of skor mutants less than WTs, while during water deprivation stress, skor plants transpired more and their leaves lost relatively less K+ than WT. This suggests a role for SKOR in water conservation under drought.

plant biology↗

Leaf hydraulic maze; Differential effect of ABA on vascular bundle-sheath, palisade, and spongy mesophyll controlling hydraulic conductance

Leaf hydraulic conductance (Kleaf) facilitates the movement of water for transpiration, enabling continual CO2 uptake while the plant maintains its water status. We hypothesized that bundle-sheath and mesophyll cells play key roles in regulating the radial flow of water out of the xylem under optimal and stress conditions. To examine that hypothesis, we generated transgenic Arabidopsis plants that were insensitive to abscisic acid (ABA) in their bundle sheath (BSabi) or mesophyll (MCabi) cells. Both BSabi and MCabi plants showed greater Kleaf and transpiration under optimal conditions. Yet, the stomatal apertures, stomatal indices and vein densities of the BSabi plants were similar to those of WT plants. MCabi plants had larger stomatal apertures, a higher stomatal index and greater vascular diameter and biomass, relative to the WT and BSabi. In response to xylem-fed ABA, both transgenic and WT plants reduced their Kleaf and transpiration. However, leaf water potential was reduced only in the WT. The membrane osmotic water permeability (Pf) of the WTs spongy mesophyll was higher than that of its palisade mesophyll. Moreover, only the spongy cells reduced their Pf in response to ABA. ABA-insensitive spongy mesophyll cells had a low Pf; whereas ABA-insensitive bundle-sheath cells had a higher Pf. Palisade cells maintained a low Pf at all ABA levels. ABA increased the symplastic water pathway, but its contribution to Kleaf was negligible. We suggest that the bundle sheath-spongy mesophyll pathway may control Kleaf to maintain steady-state conditions in the palisade cells and optimal whole-leaf water-use efficiency.

plant biology↗

Stress is basic: ABA alkalinizes both the xylem sap and the cytosol of Arabidopsis vascular bundle sheath cellsby inhibiting their P-type H+-ATPaseand stimulating their V-type H+-ATPase

BACKGROUND AND HYPOTHESIS* Under water deprivation, in many perennial species, the stress hormone, ABA, appears in the xylem sap in the shoot (including leaf) veins and the xylem sap pH (pHEXT) increases. This study aimed to test the hypothesis that ABA is the signal for an altered proton balance of the leaf-vein-enwrapping bundle sheath cells (BSCs). METHODS* Plant Material. We used a few Arabidopsis thaliana (L.) Heynh. genotypes: wildtype (WT) of two accessions, Landsberg erecta (Ler) and Columbia (Col), and a few mutants and transformants in these backgrounds. * H+-Pumps activities. We monitored ABA effects on the H+-pump activities in the BSCs cytosol-delimiting membranes (plasma membrane and tonoplast) by monitoring the cytosol and the xylem pH, and the membrane potential (EM), by imaging the fluorescence of pH- and membrane potential (EM)-reporting probes: (a) the BSCs pHEXT - with the ratiometric fluorescent dye FITC-dextran petiole-fed into detached leaves in unbuffered xylem perfusion solution (XPS), (b) the BSCs pHCYT - with the ratiometric dye SNARF1 loaded into BSCs isolated protoplasts, and (c) the BSCs EM - with the ratiometric dye di- 8-ANEPPS. RESULTS* ABA increased the pHEXT; this response was abolished in an abi1-1 mutant with impaired signaling via a PP2C (ABI1) and in an aha2-4 mutant with knocked-down AHA2; * ABA depolarized the WT BSCs; * ABA increased pHCYT irrespective of AHA2 activity (i.e., whether or not AHA was inhibited by vanadate, or in the aha2-4 mutant); * The ABA-induced cytosol alkalinization was abolished in the absence of VHA activity (i.e., when VHA was inhibited by bafilomycin A1, or in the vha-a2 vha-a3 double mutant with inactive VHA); * All these results resemble the ABA effect on GCs; * In contrast to GCs, AHA2 and not AHA1 is the ABA major target in BSCs; * Blue light (BL) enabled the response of the BSCs VHA to ABA; * The ABA- and BL-signaling pathways acting on both BSCs pumps, AHA2 and VHA, are likely to be BSCs autonomous, based on (a) the presence in the BSCs of many genes of the ABA- and BL-signaling pathways and (b) ABA responses (depolarization and pHCYT elevation) demonstrated under BL in isolated protoplasts. SIGNIFICANCE STATEMENTWe reveal here an alkalinizing effect of the plant drought-stress hormone ABA on the pH on both sides of the plasmalemma of the vein-enwrapping bundle sheath cells (BSCs), due to ABA inhibition of the BSCs AHA2, the plasmalemma H+- ATPase and stimulation of VHA, their vacuolar H+-ATPase. Since pH affects the BSCs selective regulation of solute and water fluxes into the leaf, these H+- pumps may be attractive targets for manipulations aiming to improve plant drought response.

plant biology↗

Bundle-sheath cells are internal leaf "water valves" controlled via xylem acidification by H+-ATPase

O_LIThe leaf vascular bundle sheath cells (BSCs) that tightly envelop the leaf veins, are a selective and dynamic barrier to xylem-sap water and solutes radially entering the mesophyll cells. Under normal conditions, xylem-sap pH of <6 is presumably important for driving and regulating the transmembranal solute transport. Having discovered recently a differentially high expression of a BSCs proton pump, AHA2, we now test the hypothesis that it regulates this pH and leaf radial water fluxes. C_LIO_LIWe monitored the xylem-sap pH in the veins of detached leaves of WT Arabidopsis, AHA mutants, and aha2 mutants complemented with AHA2 gene solely in BSCs. We tested an AHA inhibitor and stimulator, and different pH buffers. We monitored their impact on the xylem-sap pH and the whole leaf hydraulic conductance (Kleaf), and the effect of pH on the water osmotic permeability (Pf) of isolated BSCs protoplasts. C_LIO_LIOur results demonstrated that AHA2 is necessary for xylem-sap acidification, and in turn, for elevating Kleaf. Conversely, knocking out AHA2 alkalinized the xylem-sap. Also, elevating xylem sap pH to 7.5 reduced Kleaf and elevating external pH to 7.5 decreased the BSCs Pf. C_LIO_LIAll these demonstrate a causative link between AHA2 activity in BSCs and leaf radial water conductance. C_LI One-sentence summaryBundle-sheath cells can control the leaf hydraulic conductance by proton-pump-regulated xylem sap pH

plant biology↗

Role of guard-cell ABA in determining maximal stomatal aperture and prompt vapor-pressure-deficit response

Abscisic acid (ABA) is known to be involved in stomatal closure. However, its role in stomatal response to rapid increases in the vapor pressure deficit (VPD) is unclear. To study this issue, we generated guard cell (GC)-specific ABA-insensitive Arabidopsis plants (GC-specific abi1-1; GCabi). Under normal conditions, the stomatal conductance (gs) and apertures of GCabi plants were greater than those of control plants. This supports GC ABA role as limiting maximal stomatal aperture under non-stressful conditions. When there was a rapid increase in VPD (0.15 to 1 kPa), the gs and stomatal apertures of GCabi decreased in a manner similar that observed in the WT control, but different from that observed in WT plants treated with fusicoccin. Low VPD increased the size of the stomatal apertures of the WT, but not of GCabi. We conclude that GC ABA does not play a significant role in the initial, rapid stomatal closure that occurs in response to an increase in VPD, but is important for stomatal adaptation to ambient VPD. We propose a biphasic angiosperm VPD-sensing model that includes an initial passive-hydraulic, ABA-independent phase and a subsequent ABA-dependent steady-state phase in which stomatal behavior is optimized for ambient VPD conditions.\n\nHighlightGuard-cell ABA does not play a significant role in the immediate closure of stomata following an increase in the VPD, but is important for stomatal adaptation to ambient VPD.

plant biology↗