Romani G, Bonza M C, Filippini I, Cerana M, Beffagna N, De Michelis M I
Istituto di Biofisica del CNR-Sezione di Milano, Dipartimento di Biologia, Università degli Studi di Milano, Milano, Italy.
Plant Biol (Stuttg). 2004 Mar-Apr;6(2):192-200. doi: 10.1055/s-2004-817848.
Treatment of Arabidopsis thaliana cells with oligogalacturonides (OG) initiates a transient production of reactive oxygen species (ROS), the concentration of which in the medium peaks after about 20 min of treatment. The analysis of OG effects on Ca (2+) fluxes shows that OG influence both Ca (2+) influx and Ca (2+) efflux (measured as (45)Ca (2+) fluxes) in a complex way. During the first 10 - 15 min, OG stimulate Ca (2+) influx and decrease its efflux, while at successive times of treatment, OG cause an increase of Ca (2+) efflux and a slight decrease of its influx. Treatment with sub- micro M concentrations of eosin yellow (EY), which selectively inhibits the Ca (2+)-ATPase of plasma membrane (PM), completely prevents the OG-induced increase in Ca (2+) efflux. EY also suppresses the transient feature of OG-induced ROS accumulation, keeping the level of ROS in the medium high. The biochemical analysis of PM purified from OG-treated cells indicates that treatment with OG for 15 to 45 min induces a significant decrease in Ca (2+)-ATPase activation by exogenous calmodulin (CaM), and markedly increases the amount of CaM associated with the PM. During the same time span, OG do not influence the expression of At-ACA8, the main isoform of PM Ca (2+)-ATPase in suspension-cultured A. thaliana cells, and of CaM genes. Overall, the reported results demonstrate that the PM Ca (2+)-ATPase is involved in the response of plant cells to OG and is essential in regulation of the oxidative burst.
用寡聚半乳糖醛酸(OG)处理拟南芥细胞会引发活性氧(ROS)的短暂产生,处理约20分钟后,培养基中ROS的浓度达到峰值。对OG对Ca(2+)通量影响的分析表明,OG以复杂的方式影响Ca(2+)内流和Ca(2+)外流(以(45)Ca(2+)通量测量)。在最初的10 - 15分钟内,OG刺激Ca(2+)内流并减少其外流,而在后续处理时间,OG导致Ca(2+)外流增加,内流略有减少。用亚微摩尔浓度的曙红黄(EY)处理,其选择性抑制质膜(PM)的Ca(2+)-ATP酶,完全阻止了OG诱导的Ca(2+)外流增加。EY还抑制了OG诱导的ROS积累的短暂特征,使培养基中ROS水平保持较高。对从OG处理细胞中纯化的PM进行生化分析表明,用OG处理15至45分钟会导致外源钙调蛋白(CaM)对Ca(2+)-ATP酶激活的显著降低,并显著增加与PM相关的CaM量。在同一时间段内,OG不影响悬浮培养的拟南芥细胞中PM Ca(2+)-ATP酶的主要同工型At-ACA8和CaM基因的表达。总体而言,所报道的结果表明,PM Ca(2+)-ATP酶参与植物细胞对OG的反应,并且在氧化爆发的调节中至关重要。