首页> 美国卫生研究院文献>Plant Physiology >Inhibition of Blue Light-Dependent H+ Pumping by Abscisic Acid through Hydrogen Peroxide-Induced Dephosphorylation of the Plasma Membrane H+-ATPase in Guard Cell Protoplasts
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Inhibition of Blue Light-Dependent H+ Pumping by Abscisic Acid through Hydrogen Peroxide-Induced Dephosphorylation of the Plasma Membrane H+-ATPase in Guard Cell Protoplasts

机译:脱落酸通过过氧化氢诱导的保卫细胞原生质体中质膜H + -ATPase的去磷酸化抑制蓝光依赖性H +泵浦

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摘要

Blue light (BL)-dependent H+ pumping by guard cells, which drives stomatal opening, is inhibited by abscisic acid (ABA). We investigated this response with respect to the activity of plasma membrane H+-ATPase using Vicia guard cell protoplasts. ATP hydrolysis by the plasma membrane H+-ATPase, phosphorylation of the H+-ATPase, and the binding of 14-3-3 protein to the H+-ATPase stimulated by BL were inhibited by ABA at 10 μm. All of these responses were similarly inhibited by hydrogen peroxide (H2O2) at 1 mm. The ABA-induced inhibitions of BL-dependent H+ pumping and phosphorylation of the H+-ATPase were partially restored by ascorbate, an intracellular H2O2 scavenger. A single-cell analysis of the cytosolic H2O2 using 2′,7′-dichlorofluorescin revealed that H2O2 was generated by ABA in guard cell protoplasts. We also indicated that H+ pumping induced by fusicoccin and the binding of 14-3-3 protein to the H+-ATPase were inhibited slightly (approximately 20%) by both ABA and H2O2. By contrast, H2O2 at 1 mm did not affect H+ pumping by the H+-ATPase in microsomal membranes. From these results, we concluded that inhibition of BL-dependent H+ pumping by ABA was due to a decrease in the phosphorylation levels of H+-ATPase and that H2O2 might be involved in this response. Moreover, there are at least two inhibition sites by ABA in the BL signaling pathway of guard cells.
机译:脱落酸(ABA)抑制了由保卫细胞产生的依赖于蓝光(BL)的H + 泵浦,从而驱动了气孔的开放。我们使用蚕豆保卫细胞原生质体调查了这种反应对质膜H + -ATPase活性的影响。质膜H + -ATPase水解ATP,H + -ATPase磷酸化以及14-3-3蛋白与H +的结合BL刺激的 -ATPase在10μm处被ABA抑制。所有这些响应都类似地在1 mm处被过氧化氢(H2O2)抑制。 ABA诱导的细胞内H2O2清除剂抗坏血酸可部分恢复对BL依赖性H + 泵浦的抑制和H + -ATPase的磷酸化。使用2',7'-dichlorofluorescin对细胞质H2O2进行单细胞分析,结果表明ABA在保卫细胞原生质体中生成H2O2。我们还表明,fusicoccin诱导的H + 泵送和14-3-3蛋白与H + -ATPase的结合均受到轻微抑制(约20%)。 ABA和H2O2。相比之下,1 mm处的H2O2不会影响微粒体膜中H + -ATPase的H + 泵送。从这些结果,我们得出结论,ABA抑制BL依赖性H + 泵浦是由于H + -ATPase的磷酸化水平降低,并且H2O2可能是参与此响应。此外,在保卫细胞的BL信号传导途径中,至少有两个ABA抑制位点。

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