Coursol Sylvie, Fromentin Jérôme, Noirot Elodie, Brière Christian, Robert Franck, Morel Johanne, Liang Yun-Kuan, Lherminier Jeannine, Simon-Plas Françoise
INRA, Institut Jean-Pierre Bourgin, UMR 1318, ERL CNRS 3559, Saclay Plant Sciences, RD10, F-78026, Versailles, France.
AgroParisTech, Institut Jean-Pierre Bourgin, UMR 1318, ERL CNRS 3559, Saclay Plant Sciences, RD10, F-78026, Versailles, France.
New Phytol. 2015 Feb;205(3):1239-1249. doi: 10.1111/nph.13094. Epub 2014 Oct 10.
The proteinaceous elicitor cryptogein triggers defence reactions in Nicotiana tabacum (tobacco) through a signalling cascade, including the early production of reactive oxygen species (ROS) by the plasma membrane (PM)-located tobacco respiratory burst oxidase homologue D (NtRbohD). Sphingolipid long-chain bases (LCBs) are emerging as potent positive regulators of plant defence-related mechanisms. This led us to question whether both LCBs and their phosphorylated derivatives (LCB-Ps) are involved in the early signalling process triggered by cryptogein in tobacco BY-2 cells. Here, we showed that cryptogein-induced ROS production was inhibited by LCB kinase (LCBK) inhibitors. Additionally, Arabidopsis thaliana sphingosine kinase 1 and exogenously supplied LCB-Ps increased cryptogein-induced ROS production, whereas exogenously supplied LCBs had a strong opposite effect, which was not driven by a reduction in cellular viability. Immunogold-electron microscopy assay also revealed that LCB-Ps are present in the PM, which fits well with the presence of a high LCBK activity associated with this fraction. Our data demonstrate that LCBs and LCB-Ps differentially regulate cryptogein-induced ROS production in tobacco BY-2 cells, and support a model in which a cooperative synergism between LCBK/LCB-Ps and NtRbohD/ROS in the cryptogein signalling pathway is likely at the PM in tobacco BY-2 cells.
蛋白质激发子隐地蛋白通过信号级联反应触发烟草中的防御反应,包括位于质膜(PM)的烟草呼吸爆发氧化酶同源物D(NtRbohD)早期产生活性氧(ROS)。鞘脂长链碱(LCB)正成为植物防御相关机制的有效正向调节因子。这使我们质疑LCB及其磷酸化衍生物(LCB-P)是否参与隐地蛋白在烟草BY-2细胞中触发的早期信号传导过程。在此,我们表明LCB激酶(LCBK)抑制剂可抑制隐地蛋白诱导的ROS产生。此外,拟南芥鞘氨醇激酶1和外源提供的LCB-P可增加隐地蛋白诱导的ROS产生,而外源提供的LCB则具有强烈的相反作用,这并非由细胞活力降低所致。免疫金电子显微镜检测还显示LCB-P存在于质膜中,这与该部分存在的高LCBK活性相吻合。我们的数据表明,LCB和LCB-P对烟草BY-2细胞中隐地蛋白诱导的ROS产生具有不同的调节作用,并支持一种模型,即LCBK/LCB-P与NtRbohD/ROS在隐地蛋白信号通路中的协同增效作用可能发生在烟草BY-2细胞的质膜上。