The role of phytohormone signaling in ozone-induced cell death in plants

被引:61
作者
Tamaoki, Masanori [1 ]
机构
[1] Natl Inst Environm Studies, Div Environm Biol, 16-2 Onogawa, Tsukuba, Ibaraki 3058506, Japan
关键词
cross-talk; ethylene; jasmonic acid; ozone; phytohormones; programmed cell death; salicylic acid; signaling pathways;
D O I
10.4161/psb.3.3.5538
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ozone is the main photochemical oxidant that causes leaf damage in many plant species, and can thereby significantly decrease the productivity of crops and forests. When ozone is incorporated into plants, it produces reactive oxygen species (ROS), such as superoxide radicals and hydrogen peroxide. These ROS induce the synthesis of several plant hormones, such as ethylene, salicylic acid, and jasmonic acid. These phytohormones are required for plant growth, development, and defense responses, and regulate the extent of leaf injury in ozone-fumigated plants. Recently, responses to ozone have been studied using genetically modified plants and mutants with altered hormone levels or signaling pathways. These researches have clarified the roles of phytohormones and the complexity of their signaling pathways. The present paper reviews the biosynthesis of the phytohormones ethylene, salicylic acid, and jasmonic acid, their roles in plant responses to ozone, and multiple interactions between these phytohormones in ozone-exposed plants.
引用
收藏
页码:166 / 174
页数:9
相关论文
共 50 条
  • [41] Ethylene signaling in salt stress- and salicylic acid-induced programmed cell death in tomato suspension cells
    Poor, Peter
    Kovacs, Judit
    Szopko, Dora
    Tari, Irma
    PROTOPLASMA, 2013, 250 (01) : 273 - 284
  • [42] Nitric oxide implication in cadmium-induced programmed cell death in roots and signaling response of yellow lupine plants
    Arasimowicz-Jelonek, Magdalena
    Floryszak-Wieczorek, Jolanta
    Deckert, Joanna
    Rucinska-Sobkowiak, Renata
    Gzyl, Jaroslaw
    Pawlak-Sprada, Sylwia
    Abramowski, Dariusz
    Jelonek, Tomasz
    Gwozdz, Edward A.
    PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2012, 58 : 124 - 134
  • [43] Ozone-induced nasal hyperresponsiveness to tachykinins in guinea pigs
    Ho, Ching-Yin
    Tan, Ching-Ting
    Tsai, Hung-Huey
    Kou, Yu Ru
    AMERICAN JOURNAL OF RHINOLOGY, 2008, 22 (05): : 463 - 467
  • [44] Effects of Anesthesia on Ozone-Induced Lung and Systemic Inflammation
    Miranda L. Wilson
    Jarl A. Thysell
    Kristen K. Baumann
    Danny V. Quaranta
    W. Sandy Liang
    Michelle A. Erickson
    Lung, 2022, 200 : 269 - 275
  • [45] Ebselen decreases ozone-induced pulmonary inflammation in rats
    Ishii, Y
    Hashimoto, K
    Hirano, K
    Morishima, Y
    Mochizuki, M
    Masuyama, K
    Nomura, A
    Sakamoto, T
    Uchida, Y
    Sagai, M
    Sekizawa, K
    LUNG, 2000, 178 (04) : 225 - 234
  • [46] Prediction of ozone-induced lung function responses in humans
    McDonnell, William F.
    Stewart, Paul W.
    Smith, Marjo V.
    INHALATION TOXICOLOGY, 2010, 22 (02) : 160 - 168
  • [47] Ozone-induced airway hyperresponsiveness: roles of ROCK isoforms
    Lambert, James A.
    Song, Weifeng
    AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2015, 309 (12) : L1394 - L1397
  • [48] Stress axis variability is associated with differential ozone-induced lung inflammatory signaling and injury biomarker response
    Thomas, Jith
    Guenette, Josee
    Thomson, Errol M.
    ENVIRONMENTAL RESEARCH, 2018, 167 : 751 - 758
  • [49] Ozone-induced changes in the chloroplast structure of conifer needles, and their use in ozone diagnostics
    Kivimäenpää, M
    Selldén, G
    Sutinen, S
    ENVIRONMENTAL POLLUTION, 2005, 137 (03) : 466 - 475
  • [50] Ozone-induced effects on leaves in African crop species
    Sharps, Katrina
    Hayes, Felicity
    Harmens, Harry
    Mills, Gina
    ENVIRONMENTAL POLLUTION, 2021, 268