保卫细胞的ABA信号转导

植物激素脱落酸(ABA)调节植物体多种生理过程,尤其在一些逆境条件下,植物体中ABA大量合成,诱导气孔关闭,从而有效地调控植物体内的水分平衡.尽管人们对ABA诱导气孔关闭作用已得到共识,但有关信号转导的细节还很不清楚.该文简要介绍了研究气孔保卫细胞信号转导途径的相关技术以及与ABA信号转导直接相关的ABA受体、第二信使、蛋白质磷酸化和离子通道调节等方面的最新妍究进展.并在前人研究工作的基础上,勾画出气孔保卫细胞ABA、H2O2的信号转导模式图.     

Evidence for an Extracellular Reception Site for Abscisic Acid in Commelina Guard Cells

The phytohormone abscisic acid (ABA) triggers stomatal closing as a physiological response to drought stress. Several basic questions limit an understanding of the mechanism of ABA reception in guard cells. Whether primary ABA receptors are located on the extracellular side of the plasma membrane, within the intracellular space of guard cells, or both remains unknown. Furthermore, it is not clear whether ABA must be transported into guard cells to exert control over stomatal movements. In the present study, a combination of microinjection into guard cells and physiological assays of stomatal movements have been performed to determine primary sites of ABA reception in guard cells. Microinjection of ABA into guard cells of Commelina communis L. resulted in injected cytosolic concentrations of 50 to 200 [mu]M ABA and in additional experiments in lower concentrations of approximately 1 [mu]M ABA. Stomata with ABA-loaded guard cells (n > 180) showed opening similar to stomata with uninjected guard cells. The viability of guard cells following ABA injection was demonstrated by neutral red staining as well as monitoring of stomatal opening. Extracellular application of 10 [mu]M ABA inhibited stomatal opening by 98% at pH 6.15 and by 57% at pH 8.0. The pH dependence of extracellular ABA action may suggest a contribution of an intracellular ABA receptor to stomatal regulation. The findings presented here show that intracellular ABA alone does not suffice to inhibit stomatal opening under the imposed conditions. Furthermore, these data provide evidence that a reception site for ABA-mediated inhibition of stomatal opening is on the extracellular side of the plasma membrane of guard cells.     

Role of Calcium in Signal Transduction of Commelina Guard Cells

The role of cytosolic Ca2+ in signal transduction in stomatal guard cells of Commelina communis was investigated using fluorescence ratio imaging and photometry. By changing extracellular K+, extracellular Ca2+, or treatment with Br-A23187, substantive increases in cytosolic Ca2+ to over 1 micromolar accompanied stomatal closure. The increase in Ca2+ was highest in the cytoplasm around the vacuole and the nucleus. Similar increases were observed when the cells were pretreated with ethyleneglycol-bis-(o-aminoethyl)tetraacetic acid or the channel blocker La3+, together with the closing stimuli. This suggests that a second messenger system operates between the plasma membrane and Ca2+-sequestering organelle(s). The endogenous growth regulator abscisic acid elevated cytosolic Ca2+ levels in a minority of cells investigated, even though stomatal closure always occurred. Ca2+-dependent and Ca2+-independent transduction pathways linking abscisic acid perception to stomatal closure are thus indicated.     

植物ABA受体及其介导的信号转导通路

ABA是调控植物体生长发育和响应外界应激的重要植物激素之一。近年来, ABA受体的筛选和鉴定取得了突破性进展, 为植物中ABA信号转导通路的阐明奠定了重要基础。该文主要综述了ABA-binding protein/H subunit of Mgchelatase (ABAR/CHLH)、G protein-coupled receptor 2 (GCR2)、GPCR-type G protein 1/2 (GTG1/2)和pyrabactin resistant/PYR-like/regulatory component of ABA (PYR/PYL/RCAR)被报道为ABA受体的研究历程, 重点介绍了以ABAR/CHLH PYR/PYL/RCAR为受体的ABA信号转导通路模型的构建, 旨在为ABA受体及其信号转导通路的相关研究提供参考。     

Metabolism of Abscisic Acid in Guard Cells of Vicia faba L. and Commelina communis L

Metabolism of abscisic acid (ABA) was investigated in isolated guard cells and in mesophyll tissue of Vicia faba L. and Commelina communis L. After incubation in buffer containing [G-³H]±ABA, the tissue was extracted by grinding and the metabolites separated by thin layer chromatography. Guard cells of Commelina metabolized ABA to phaseic acid (PA), dihydrophaseic acid (DPA), and alkali labile conjugates. Guard cells of Vicia formed only the conjugates. Mesophyll cells of Commelina accumulated DPA while mesophyll cells of Vicia accumulated PA. Controls showed that the observed metabolism was not due to extracellular enzyme contaminants nor to bacterial action.

Metabolism of ABA in guard cells suggests a mechanism for removal of ABA, which causes stomatal closure of both species, from the stomatal complex. Conversion to metabolites which are inactive in stomatal regulation, within the cells controlling stomatal opening, might precede detectable changes in levels of ABA in bulk leaf tissue. The differences observed between Commelina and Vicia in metabolism of ABA in guard cells, and in the accumulation product in the mesophyll, may be related to differences in stomatal sensitivity to PA which have been reported for these species.

     

Effects of Calcium and Abscisic Acid on Volume Changes of Guard Cell Protoplasts of Commelina

Calcium ions contracted guard cell protoplasts (GCP) of Commelinacommunis L., being particularly effective within the concentrationrange of 0 to 0.2 mol m^–3. Abscisic acid (ABA) in thepresence of EGTA, which chelates free Ca²⁺ in the medium, contractedGCP to a similar extent to Ca²⁺ alone or Ca²⁺ and ABA together.Similarly, ABA in the absence of free Ca²⁺ (i.e. an ABA/EGTAtreatment) inhibited K⁺-induced swelling of contracted GCP,as did Ca²⁺ alone or ABA and Ca²⁺ together. Lanthanum, a Ca²⁺channel blocker, prevented the contraction of GCP by Ca²⁺ buthad no effect if ABA was also present with Ca²⁺. The inhibitionof swelling of GCP by Ca²⁺ was also prevented by the presenceof lanthanum or verapamil (another Ca²⁺ channel blocker). These results indicate that Ca²⁺ and ABA can act independentlyof each other in contracting swollen GCP and in preventing K⁺-inducedswelling of contracted GCP of C. communis. If swelling and contractionof GCP are equivalent to stomatal opening and closure, respectively,the results do not support the hypothesis that ABA opens Ca²⁺channels in the plasma membrane of guard cells allowing Ca²⁺to enter the cells and, as a second messenger, to set in motionclosing processes. Key words: Abscisic acid, calcium, guard cell protoplasts, stomata     

Responses of Commelina communis L. Guard Cell Protoplasts to Abscisic Acid

Fitzsimons, P. J. and Weyers, J. D. B. 1987. Responses of Commelinacommunis L. guard cell protoplasts to abscisic acid.—J.exp. Bot. 38: 992–1001. Guard cell protoplasts (GCPs) isolated from the leaf epidermisof Commelina communis L. responded to abscisic acid (ABA) ina manner which was qualitatively and quantitatively similarto that of intact stomata. ABA inhibited swelling of GCPs underlow-CO₂ conditions and swollen GCPs responded to the hormoneby shrinking. Both the absolute volume decrease and the initialrate of shrinking were commensurate with the extent and ratesof solute loss computed for ABA-treated intact, open stomata.This indicates that GCPs represent a suitable experimental systemfor studies of ABA-mediated solute fluxes. A radiotracer equilibrationmethod was developed for the rapid estimation of GCP osmoticvolume changes. Using this technique it was found that, on average,82% of the reduction in solute content caused by ABA treatmentwas due to the loss of K⁺. It is envisaged that electroneutralitymight be maintained during ABA-induced shrinkage of GCPs bynet inward proton movement leading to acidification of the vacuole. Key words: Abscisic acid, Commelina communis L., guard cells, protoplasts     

Functional Epidermal Cells are Necessary for Abscisic Acid Effects on Guard Cells

Experimental results are presented which show that abscisicacid (ABA) causes stomatal closure only if the stomatal complexis adjacent to live epidermal cells. It is further shown thatABA acts by affecting solute fluxes into and out of epidermaland guard cells. Live epidermal cells function as recipientsfor solutes and thereby assist their movement out of the guardcells. ABA-mediated solute leakage from guard cells alone doesnot suffice to cause stomatal closure within one hour.     

Effects of Fusicoccin in 'Isolated' Guard Cells of Commelina communis L

The effects of 3 ? 10^–2 mol m^–3 FC on rubidium fluxesand contents in isolated guard cells of Commelina communis L.have been studied using ⁸⁶RbCl. Fusicoccin causes a marked stimulationof influx and an immediate, apparently irreversible, decreasein efflux of ⁸⁶Rb. The effect on influx is usually more importantin determining the new net flux of Rb. Observed fluxes differmarkedly from those predicted by the Goldman-Hodgkin-Katz equation,suggesting that FC does not act solely via an effect upon theplasmalemma potential. Fusicoccin appears to have a more directeffect upon the ion movements associated with changes in stomatalaperture than either ABA or transfer to the dark. Observed changesin Rb content cannot account fully for the osmotic changes associatedwith aperture increase. Key words: Fusicoccin, Guard cells, Ion fluxes, Commelina communis     

Abscisic Acid may Mediate the Rapid Thermal Acclimatization of Photosynthesis in Wheat

Exposing cold-grown (6°C) plants of a winter cultivar (Avalon)and a spring cultivar (Highbury) of wheat to a single warm night(18 h and 25°C) significantly increased the photosyntheticrate and stomatal conductance of fully-expanded leaves withoutaffecting the calculated, substomatal CO₂ pressure. Prior to the warm-night treatment net photosynthesis and stomatalconductance in Avalon were very small at high leaf temperaturesduring measurement (25–30°C). Such high temperatureinhibitions were not observed in Highbury. Exposure to the warm-nighttreatment alleviated these inhibitions in Avalon. Consequently,the temperature response of photosynthesis was similar in theleaves of the treated cultivars and showed a relatively broadoptimum. The application of exogenous abscisic acid in the transpirationstream to the leaves of treated plants caused a reduction ofsimilar proportions in the steady-state rate of photosynthesisand in stomatal conductance and essentially reversed the effectsof the warm-night treatment in a manner which depended on thecultivar. The endogenous abscisic acid content of leaves declinedby 50% during the warm-night treatment. In conjunction, thesedata suggest that changes in the content of abscisic acid inthe leaf may regulate the observed temperature acclimatizationof apparent photosynthesis in the fully-expanded leaves of cold-grownwheat. Key words: Abscisic acid, photosynthesis, stomatal conductance, temperature, acclimatizatio     

Effects of ABA in 'Isolated' Guard Cells of Commelina communis L.

The effects of 2 x 10^–3 M ABA on ion fluxes in isolatedguard cells of Commelina communis L. have been studied, using⁸⁶RbCl and K⁸²Br, in epidermal strips in which all cells otherthan guard cells have been killed by treatment at low pH. Theeffect of ABA on influx is small, if present, and the majoreffect is a marked transient stimulation of the efflux of both⁸⁶Rb and ⁸²Br at the plasmalemma; there is also an increasein the flux of ⁸²Br from vacuole to cytoplasm. The stimulationis transient, and the cells do not simply become more leaky.The results are not consistent with previous speculations onthe mechanism by which ABA reduces aperture.     

Effects of Cations and Abscisic Acid on Chlorophyll a Fluorescence in Guard Cells of Vicia faba

The effects of cations and abscisic acid on chloroplast activity in guard cells of Vicia faba were investigated by analysis of the transient of chlorophyll a fluorescence. When epidermal strips containing guard cells as the only living cells were incubated in water and illuminated with strong light, chlorophyll a fluorescence rose rapidly to a high intensity and then declined slowly to a stationary level. The rate of this decline was enhanced by K⁺ or Na⁺, and the effect of these cations was greater when added with phosphate than with chloride as the anion. Ca²⁺ suppressed the enhancement by Na⁺ and, to a lesser extent, that by K⁺. Abscisic acid also suppressed the enhancement by K⁺ and Na⁺. Since the fluorescence decline reflects the increase of intrathylakoid H⁺ concentration necessary for photophosphorylation, the acceleration of the decline by K⁺ (or Na⁺ in the absence of Ca²⁺) implicates chloroplast activity in ion accumulation by guard cells in the light. The differential effects of phosphate and chloride suggest that chloroplast activity may be involved in malate formation in guard cells in the light.     

The Roles of CATALASE2 in Abscisic Acid Signaling in Arabidopsis Guard Cells

We investigated the roles of catalase (CAT) in abscisic acid (ABA)-induced stomatal closure using a cat2 mutant and an inhibitor of CAT, 3-aminotriazole (AT). Constitutive reactive oxygen species (ROS) accumulation due to the CAT2 mutation and AT treatment did not affect stomatal aperture in the absence of ABA, whereas ABA-induced stomatal closure, ROS production, and [Ca²⁺]_cyt oscillation were enhanced.     

Anion-Channel Blockers Inhibit S-Type Anion Channels and Abscisic Acid Responses in Guard Cells

The effects of anion-channel blockers on light-mediated stomatal opening, on the potassium dependence of stomatal opening, on stomatal responses to abscisic acid (ABA), and on current through slow anion channels in the plasma membrane of guard cells were investigated. The anion-channel blockers anthracene-9-carboxylic acid (9-AC) and niflumic acid blocked current through slow anion channels of Vicia faba L. guard cells. Both 9-AC and niflumic acid reversed ABA inhibition of stomatal opening in V. faba L. and Commelina communis L. The anion-channel blocker probenecid also abolished ABA inhibition of stomatal opening in both species. Additional tests of 9-AC effects on stomatal aperture in Commelina revealed that application of this anion-channel blocker allowed wide stomatal opening under low (1 mM) KCI conditions and increased the rate of stomatal opening under both low and high (100 mM) KCI conditions. These results indicate that anion channels can function as a negative regulator of stomatal opening, presumably by allowing anion efflux and depolarization, which prohibits ion up-take in guard cells. Furthermore, 9-AC prevented ABA induction of stomatal closure. A model in which ABA activation of anion channels contributes a rate-limiting mechanism during ABA-induced stomatal closure and inhibition of stomatal opening is discussed.     

Disruption of Microtubules by Abscisic Acid in Guard Cells of Vicia faba L.

ABA disrupted cortical microtubules in guard cells, but notin epidermal cells, with concomitant closure of stomata. Otherplant growth regulators did not disrupt the microtubles in guardcells. Thus disrution of microtubules seems to be a specificeffect of ABA in guard cells but its physiological significanceremains obscure. (Received September 11, 1995; Accepted April 26, 1996)     

Regulation of ADPGlucose Synthesis in Guard Cells of Commelina communis

The activator specificity of the ADPglucose pyrophosphorylase from Commelina communis guard cells is the same as observed for the mesophyll cell enzyme. 3-Phosphoglycerate was found to be the most effective activator. Fifty per cent of maximal stimulation was observed at about 100 micromolar. Inorganic phosphate was found to be a potent inhibitor giving 50% inhibition at 0.3 millimolar. These results are discussed with respect to regulation of starch synthesis in guard cells.     

Modeling the Calcium Signaling in Stomatal Guard Cells under the Action of Abscisic Acid

A theoretical model of calcium signaling is presented that simulates oscillations of cytoplasmic calcium concentration ([Ca²⁺]_cyt) in stomatal guard cells under the action of abscisic acid. The model is based on the kinetics of inositol 1,4,5-trisphosphate-sensitive calcium channels of endoplasmic reticulum and cyclic ADP-ribose-sensitive calcium channels of the tonoplast. The operation of two energy-dependent pumps—the Ca²⁺-ATPase of the endoplasmic reticulum and the Ca²⁺/H⁺ antiporter of the tonoplast—is also included in the model. It is shown that the removal of excessive Ca²⁺ from the cytoplasm by the tonoplast Ca²⁺/H⁺ antiporter is the main factor accounting for generation of [Ca²⁺]_cyt oscillations at a wide range of ABA concentrations (0.01–1 M). The long period of [Ca²⁺]_cyt oscillations in plant cells is explained by a slow release from inhibition of inositol 1,4,5-trisphosphate-gated calcium channels.     

Focus on Water: Intertissue Signal Transfer of Abscisic Acid from Vascular Cells to Guard Cells

Abscisic acid (ABA) is a phytohormone that responds to environmental stresses, such as water deficiency. Recent studies have shown that ABA biosynthetic enzymes are expressed in the vascular area under both nonstressed and water-stressed growth conditions. However, specific cells in the vasculature involved in ABA biosynthesis have not been identified. Here, we detected the expression of two genes encoding ABA biosynthetic enzymes, ABSCISIC ACID DEFICIENT2 and ABSCISIC ALDEHYDE OXIDASE3, in phloem companion cells in vascular tissues. Furthermore, we identified an ATP-binding cassette transporter, Arabidopsis thaliana ABCG25 (AtABCG25), expressed in the same cells. Additionally, AtABCG25-expressing Spodoptera frugiperda9 culture cells showed an ABA efflux function. Finally, we observed that enhancement of ABA biosynthesis in phloem companion cells induced guard cell responses, even under normal growth conditions. These results show that ABA is synthesized in specific cells and can be transported to target cells in different tissues.Hormones are chemical substances that exert a biochemical action on target cells at low concentrations. All multicellular organisms, including animals and plants, produce hormones to control their physiological status. In animals, many ordinary hormones are secreted from specific cells (such as endocrine cells) and transported to their target sites in other areas of the body. However, it remains unclear whether the concept of hormones as defined in animals is applicable to plants, because plant hormones are not generally synthesized in specific cells but are broadly produced (Weyers and Paterson, 2001; Gaspar et al., 2003; Forestan and Varotto, 2012).Abscisic acid (ABA) is a key phytohormone that prevents water loss from the plant body by acting on guard cells, of which stomata (epidermal pores) compose the aerial organs in plants (Hetherington, 2001; Schroeder et al., 2001; Fan et al., 2004; Joshi-Saha et al., 2011). Gene and protein expression analyses using antisense RNA or antibodies specific for ABA biosynthetic enzymes in Arabidopsis (Arabidopsis thaliana) have shown that parenchyma cells in vascular bundles are the abundant expression site of ABA biosynthesis under drought stress and well-watered growth conditions (Cheng et al., 2002; Koiwai et al., 2004; Endo et al., 2008). Because the vasculature is separated from guard cells, it has been suggested that ABA is transported from the site of synthesis to the site of action (Seo and Koshiba, 2011).We previously found that an ATP-binding cassette (ABC) transporter family, Arabidopsis thaliana ABCG25 (AtABCG25), is expressed mainly in vascular tissues, and it is expected to function as an ABA exporter that transports ABA from inside to outside cells (Kuromori et al., 2010). According to this observation, we have proposed a working model: ABA is exported from ABA-synthesizing cells in vascular tissues by AtABCG25 to reach distant guard cells and induce stomatal closure (Kuromori and Shinozaki, 2010; Umezawa et al., 2010, 2011). However, the parenchyma cells in vascular tissues expressing ABA biosynthetic enzymes or AtABCG25 transporting factor have not been identified.Here, we explored whether specific cells express ABA biosynthetic enzymes or an ABA transporter and found that their genes were expressed in phloem companion cells of vascular tissues. ABA synthesis in these cells enhances transsignaling to distant guard cells of the epidermis. These results show that ABA is synthesized in specific cells and transported to target cells in another tissue. This result is similar to endocrine hormones in animals and suggests that the ABA transport pathway between tissues in plants may be associated with specific transporters.     

脱落酸受体及其信号转导

扼要介绍RNA结合蛋白FCA、编码Mg离子螯合酶的H亚基ABAR／CHLH和G蛋白偶联受体GCR2三种脱落酸受体的生物化学和分子生物学特性以及受体信号转导途径的研究进展。     

Effect of Abscisic Acid on Cell-Wall Metabolism in Guard Cells of Vicia faba L.

Cell-wall synthesis in guard cells of Vicia faba L. was examinedusing sonicated epidermal strips incubated with [¹⁴C]glucose.The cell walls of the guard cells incorporated [¹⁴C]glucoseat a lower level in the dark than in the light. Stomatal aperturein the epidermal strips was reduced by application of 1 µmabscisic acid (ABA) in the light but not in the dark. The ABAtreatment reduced the incorporation of [¹⁴C]glucose into thecell walls especially in the light. Fractionation of the labeledcell-wall components revealed that ABA inhibited the synthesisof pectic substances and cellulose, but did not affect hemicellulosesynthesis. Microautoradiographs of the cell-wall fraction ofthe epidermal strips showed that a large amount of radioactivitywas distributed at both ends of the guard cells in the absenceof ABA and that removal of pectic substances from the cell-wallfraction resulted in uniform distribution of the radioactivityin the cell walls of the guard cells. These results indicatedthat the synthesis of pectic substances was active at both endsof the guard cells and was inhibited by ABA. Measurement ofspecific activities of neutral sugars in the guard-cell wallsshowed that polymers composed of galactose underwent activeturnover and that synthesis of glucans was inhibited by ABA.These results revealed a strong correlation between the stomatalmovement and the synthesis of pectic substances and cellulosein the guard cells, suggesting that the cell-wall metabolismin the guard cells may play a role in the regulation of stomatalmovement. (Received October 9, 1987; Accepted March 9, 1988)