Hausmann N, Fengler S, Hennig A, Franz-Wachtel M, Hampp R, Neef M
Physiological Ecology of Plants, University of Tübingen, Tübingen, Germany.
Plant Biol (Stuttg). 2014 Jan;16 Suppl 1:120-8. doi: 10.1111/plb.12051. Epub 2013 Jul 22.
Callus cell cultures of Arabidopsis thaliana (cv. Columbia) were exposed to parabolic flights in order to assess molecular, short-term responses to altered gravity fields. Using transgenic cell lines, hydrogen peroxide (H2 O2 ) and cytosolic Ca(2+) were continuously monitored. In parallel, the metabolism of samples was chemically quenched (RNAlater, Ambion for RNA; acid/base for NADPH, NADP) at typical stages of a parabola [1 g before pull up; end of pull up (1.8 g), end of microgravity (20 s) and end of pull out (1.8 g)]. Cells exhibited an increase in both Ca(2+) and H2 O2 with the onset of microgravity, and a decline thereafter. This behaviour was accompanied by a decrease of the NADPH/NADP redox ratio, indicating Ca(2+) -dependent activation of a NADPH oxidase. Microarray analyses revealed concomitant expression profiles. At the end of the microgravity phase, 396 transcripts were specifically up-, while 485 were down-regulated. Up-regulation was dominated by Ca(2+) - and ROS-related gene products. The same material was also used for analysis of phosphopeptides with 2-D SDS PAGE. Relevant spots were identified by liquid chromatography-MS. With the exception of a chaperone (HSP 70-3), hypergravity (1.8 g) and microgravity modified different sets of proteins. These are partly involved in primary metabolism (glycolysis, gluconeogenesis, citrate cycle) and detoxification of ROS. Taken together, these data show that both gene expression and protein modulation jointly respond within seconds to alterations in the gravity field, with a focus on metabolic adaptation, signalling and control of ROS.
将拟南芥(哥伦比亚生态型)的愈伤组织细胞培养物进行抛物线飞行实验,以评估其对重力场改变的分子层面短期响应。利用转基因细胞系,持续监测过氧化氢(H₂O₂)和胞质Ca²⁺。同时,在抛物线的典型阶段(拉起前1g;拉起结束时(1.8g)、微重力结束时(20s)和拉出结束时(1.8g)),对样品代谢进行化学淬灭(用于RNA的RNAlater,安比昂公司产品;用于NADPH、NADP的酸/碱)。细胞在微重力开始时Ca²⁺和H₂O₂均增加,之后下降。这种行为伴随着NADPH/NADP氧化还原比值的降低,表明Ca²⁺依赖性激活了NADPH氧化酶。微阵列分析揭示了相应的表达谱。在微重力阶段结束时,396个转录本特异性上调,485个转录本下调。上调主要由Ca²⁺和ROS相关基因产物主导。相同材料也用于二维SDS-PAGE分析磷酸肽。通过液相色谱-质谱鉴定相关斑点。除了一种伴侣蛋白(HSP 70-3)外,超重力(1.8g)和微重力改变了不同的蛋白质组。这些蛋白质部分参与初级代谢(糖酵解、糖异生、柠檬酸循环)和ROS解毒。综上所述,这些数据表明基因表达和蛋白质调节在数秒内共同响应重力场的改变,重点在于代谢适应、信号传导和ROS控制。