The soluble proteome of tobacco Bright Yellow-2 cells undergoing H2O2-induced programmed cell death

被引:15
|
作者
Vannini, Candida [1 ]
Marsoni, Milena [1 ]
Cantara, Carlo [1 ]
De Pinto, Maria Concetta [2 ]
Locato, Vittoria [3 ]
De Gara, Laura [3 ]
Bracale, Marcella [1 ]
机构
[1] Univ Insubria, Dipartimento Biotecnol & Sci Vita, I-21100 Varese, Italy
[2] Univ Bari, Dipartimento Biol, I-70125 Bari, Italy
[3] Univ Campus Biomed Roma, Ctr Integrato Ric, I-00128 Rome, Italy
关键词
H2O2; PCD; proteome; redox homeostasis; TBY-2; cells; CYTOSOLIC ASCORBATE PEROXIDASE; HYDROGEN-PEROXIDE; NITRIC-OXIDE; HEAT-SHOCK; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; ENDOPLASMIC-RETICULUM; STRESS RESPONSES; REDOX REGULATION; GENE-EXPRESSION; BY-2; CELLS;
D O I
10.1093/jxb/ers031
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plant programmed cell death (PCD) is a genetically controlled process that plays an important role in development and stress responses. Reactive oxygen species (ROS) are key inducers of PCD. The addition of 50 mM H2O2 to tobacco Bright Yellow-2 (TBY-2) cell cultures induces PCD. A comparative proteomic analysis of TBY-2 cells treated with 50 mM H2O2 for 30 min and 3 h was performed. The results showed early down-regulation of several elements in the cellular redox hub and inhibition of the protein repair-degradation system. The expression patterns of proteins involved in the homeostatic response, in particular those associated with metabolism, were consistently altered. The changes in abundance of several cytoskeleton proteins confirmed the active role of the cytoskeleton in PCD signalling. Cells undergoing H2O2-induced PCD fail to cope with oxidative stress. The antioxidant defence system and the anti-PCD signalling cascades are inhibited. This promotes a genetically programmed cell suicide pathway. Fifteen differentially expressed proteins showed an expression pattern similar to that previously observed in TBY-2 cells undergoing heat shock-induced PCD. The possibility that these proteins are part of a core complex required for PCD induction is discussed.
引用
收藏
页码:3137 / 3155
页数:19
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