Chang Xiaoli, Riemann Michael, Liu Qiong, Nick Peter
Department of Plant Pathology, Agricultural College, Sichuan Agricultural University, Chengdu 611130, P. R. China.
Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology, Kaiserstr. 2, D-76128 Karlsruhe, Germany.
PLoS One. 2015 May 1;10(5):e0125498. doi: 10.1371/journal.pone.0125498. eCollection 2015.
Plant innate immunity is composed of two layers--a basal immunity, and a specific effector-triggered immunity, which is often accompanied by hypersensitive cell death. Initiation of cell death depends on a complex network of signalling pathways. The phytohormone auxin as central regulator of plant growth and development represents an important component for the modulation of plant defence. In our previous work, we showed that cell death is heralded by detachment of actin from the membrane. Both, actin response and cell death, are triggered by the bacterial elicitor harpin in grapevine cells. In this study we investigated, whether harpin-triggered actin bundling is necessary for harpin-triggered cell death. Since actin organisation is dependent upon auxin, we used different auxins to suppress actin bundling. Extracellular alkalinisation and transcription of defence genes as the basal immunity were examined as well as cell death. Furthermore, organisation of actin was observed in response to pharmacological manipulation of reactive oxygen species and phospholipase D. We find that induction of defence genes is independent of auxin. However, auxin can suppress harpin-induced cell death and also counteract actin bundling. We integrate our findings into a model, where harpin interferes with an auxin dependent pathway that sustains dynamic cortical actin through the activity of phospholipase D. The antagonism between growth and defence is explained by mutual competition for signal molecules such as superoxide and phosphatidic acid. Perturbations of the auxin-actin pathway might be used to detect disturbed integrity of the plasma membrane and channel defence signalling towards programmed cell death.
植物先天免疫由两层组成——基础免疫和特定的效应子触发免疫,后者通常伴随着超敏细胞死亡。细胞死亡的起始取决于一个复杂的信号通路网络。植物激素生长素作为植物生长发育的核心调节因子,是调节植物防御的重要组成部分。在我们之前的工作中,我们表明肌动蛋白从膜上脱离预示着细胞死亡。肌动蛋白反应和细胞死亡均由葡萄细胞中的细菌激发子harpin触发。在本研究中,我们调查了harpin触发的肌动蛋白成束是否是harpin触发细胞死亡所必需的。由于肌动蛋白的组织依赖于生长素,我们使用不同的生长素来抑制肌动蛋白成束。检测了作为基础免疫的细胞外碱化和防御基因的转录以及细胞死亡情况。此外,还观察了肌动蛋白的组织对活性氧和磷脂酶D的药理学操作的反应。我们发现防御基因的诱导不依赖于生长素。然而,生长素可以抑制harpin诱导的细胞死亡,也可以抵消肌动蛋白成束。我们将我们的发现整合到一个模型中,其中harpin干扰了一条依赖生长素的途径,该途径通过磷脂酶D的活性维持动态的皮质肌动蛋白。生长与防御之间的拮抗作用是由对超氧化物和磷脂酸等信号分子的相互竞争来解释的。生长素-肌动蛋白途径的扰动可能被用于检测质膜完整性的破坏,并将防御信号导向程序性细胞死亡。