Maffei Massimo E, Mithöfer Axel, Arimura Gen-Ichiro, Uchtenhagen Hannes, Bossi Simone, Bertea Cinzia M, Starvaggi Cucuzza Laura, Novero Mara, Volpe Veronica, Quadro Stefano, Boland Wilhelm
Department of Plant Biology and Centre of Excellence CEBIOVEM, University of Turin, Italy.
Plant Physiol. 2006 Mar;140(3):1022-35. doi: 10.1104/pp.105.071993. Epub 2006 Jan 27.
In response to herbivore (Spodoptera littoralis) attack, lima bean (Phaseolus lunatus) leaves produced hydrogen peroxide (H(2)O(2)) in concentrations that were higher when compared to mechanically damaged (MD) leaves. Cellular and subcellular localization analyses revealed that H(2)O(2) was mainly localized in MD and herbivore-wounded (HW) zones and spread throughout the veins and tissues. Preferentially, H(2)O(2) was found in cell walls of spongy and mesophyll cells facing intercellular spaces, even though confocal laser scanning microscopy analyses also revealed the presence of H(2)O(2) in mitochondria/peroxisomes. Increased gene and enzyme activations of superoxide dismutase after HW were in agreement with confocal laser scanning microscopy data. After MD, additional application of H(2)O(2) prompted a transient transmembrane potential (V(m)) depolarization, with a V(m) depolarization rate that was higher when compared to HW leaves. In transgenic soybean (Glycine max) suspension cells expressing the Ca(2+)-sensing aequorin system, increasing amounts of added H(2)O(2) correlated with a higher cytosolic calcium (Ca(2+)) concentration. In MD and HW leaves, H(2)O(2) also triggered the increase of Ca(2+), but MD-elicited Ca(2+) increase was more pronounced when compared to HW leaves after addition of exogenous H(2)O(2). The results clearly indicate that V(m) depolarization caused by HW makes the membrane potential more positive and reduces the ability of lima bean leaves to react to signaling molecules.
为响应草食动物(埃及棉铃虫)的攻击,利马豆(菜豆)叶片产生的过氧化氢(H₂O₂)浓度高于机械损伤(MD)叶片。细胞和亚细胞定位分析表明,H₂O₂主要定位于MD和草食动物损伤(HW)区域,并扩散到整个叶脉和组织中。优先在面向细胞间隙的海绵状细胞和叶肉细胞的细胞壁中发现H₂O₂,尽管共聚焦激光扫描显微镜分析也显示线粒体/过氧化物酶体中存在H₂O₂。HW后超氧化物歧化酶的基因和酶活性增加与共聚焦激光扫描显微镜数据一致。MD后,额外施加H₂O₂促使跨膜电位(Vₘ)短暂去极化,其Vₘ去极化速率高于HW叶片。在表达Ca²⁺传感水母发光蛋白系统的转基因大豆(大豆)悬浮细胞中,添加的H₂O₂量增加与更高的胞质钙([Ca²⁺]cyt)浓度相关。在MD和HW叶片中,H₂O₂也引发了[Ca²⁺]cyt的增加,但与添加外源H₂O₂后的HW叶片相比,MD引发的[Ca²⁺]cyt增加更为明显。结果清楚地表明,HW引起的Vₘ去极化使膜电位更正,并降低了利马豆叶片对信号分子的反应能力。