• 关键词：AlCl₃  NO  蚕豆保卫细胞  细胞程序性死亡

• 基金项目：国家自然科学基金项目(No.30870454, 30470318);山西省回国留学人员科研资助项目(No.2012013); 山西省科技攻关项目(No.20120322008-02)

• 王毅
• 山西大学生命科学学院, 太原 030006

• 仪慧兰
• 山西大学生命科学学院, 太原 030006

• 摘要：铝(Al)是地壳中含量最丰富的金属元素,是酸性土壤中导致植物生长抑制和作物产量下降的一个主要因素,但铝毒性作用机制尚不清楚.本文以蚕豆叶表皮为材料,研究铝胁迫对气孔保卫细胞活性的影响,探讨NO在铝诱导细胞死亡中的作用.结果表明,一定浓度的AlCl₃可诱导气孔保卫细胞活性降低,部分细胞死亡,且随着铝浓度的增高细胞死亡率增高.死细胞呈现核固缩、核崩解、凋亡小体等典型凋亡特征,且凋亡抑制剂Z-Asp-CH₂-DCB能阻止AlCl₃诱发的细胞死亡.用NO清除剂c-PTIO、NO合酶抑制剂L-NAME或硝酸还原酶抑制剂NaN₃降低铝处理组胞内NO后,细胞死亡率显著降低,胞内ROS、Ca²⁺水平同期降低;NaN₃还能降低铝处理组中具有程序性死亡特征的细胞比率.用ROS清除剂AsA清除铝处理组胞内ROS后,细胞死亡率显著降低,胞内Ca²⁺和NO水平亦显著降低;铝处理液中加入Ca²⁺通道抑制剂LaCl₃后,细胞死亡率低于铝单独处理组,胞内ROS和NO水平无明显改变。研究结果表明,铝胁迫引起的胞内NO合成增加通过Ca²⁺信号途径介导了保卫细胞的程序性死亡.

• Abstract：Aluminum (Al) is the most abundant metallic element in the earth's crust. It has been found that Al is a major factor reducing plant growth and crop production in acid soils. However, the mechanism of aluminum toxicity is still not completely clear. In this study, effect of aluminum on guard cell viability was investigated in V. faba leaves. Epidermal strips were obtained by peeling off the lower epidermis from young fully expanded leaves, incubated in 2-(N-morpholino) ethanesulfonic acid (MES) buffer containing some chemicals (AlCl₃ with or without some alleviants) for 3 h, and then stained with fluorescein diacetate (FDA) to show cell viability. Alternative staining agents in this experiment include 2',7'-dichlorofluorescein diacetate (DCFH-DA), 3-Amino,4-aminomethyl-2',7'-difluorescein diacetate (DAF-FM DA) and fluo-3 acetomethoxyester (Fluo-3AM) to indicate intracellular ROS, NO and Ca²⁺ levels. The results showed that aluminum treatment significantly decreased cell viability at concentrations of 0.2 to 10 mmol·L^-1. A synchronous increase in cell death rate and intracellular NO, ROS and Ca²⁺ levels occurred in V. faba guard cells exposure to aluminum. Typical features of programmed cell death including nuclear condensation, fragmentation and apoptotic bodies were found in Al-treated guard cells, and could be reversed by caspases inhibitor Z-Asp-2,6-dichlorobenzoyloxymethylketone (Z-Asp-CH₂-DCB), demonstrating a programmed cell death caused by aluminum toxicity. After application of NO scavenger c-PTIO, NO synthase inhibitor L-NAME or nitrite reductase inhibitor NaN₃ to inhibit the elevation of intracellular NO in guard cells evoked by aluminum, Al-induced cell death rate significantly decreased, and the intracellular ROS and Ca²⁺ levels in guard cells also decreased. NaN₃ can also decrease PCD rate in aluminum treatment groups. Antioxidant substance ascorbic acid (AsA) decreased Al-induced cell death and also the levels of intracellular NO and Ca²⁺ levels in aluminum treatment groups. Application of LaCl₃, a plasma membrane Ca²⁺ channel blocker, significantly decreased Al-induced cell death. Our results suggest that Al-induced cell death in V. faba guard cells could be one kind of programmed cell death mediated by NO generation and activation of cytosolic Ca²⁺ signaling.

• Key words：AlCl₃  NO  V. faba guard cell  programmed cell death

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