Oxidant and antioxidant signalling in plants: a re-evaluation of the concept of oxidative stress in a physiological context

By Christine H. Foyer, G. Noctor. 2005

1,913 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/282b1c52a73dc710e5b96ad473a3dd2be414f365

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Citations in the corpus

Transcriptomic Footprints Disclose Specificity of Reactive Oxygen Species Signaling in Arabidopsis1[W] (2006, background): “developmental processes, including biotic and abiotic stress responses, allelopathic plant-plant interactions, cell division and elongation, and programmed cell death (Pei et al., 2000; Bethke and Jones, 2001; Foreman et al., 2003; Bais et al., 2003; Apel and Hirt, 2004; Foyer and Noctor, 2005).”
Oxidative modifications to cellular components in plants. (2007, background): “It is generally observed that ROS production and ROS-induced damage increase during abiotic and biotic stress and ROS are important signaling molecules (5, 33, 36, 67).”
The Multiple Origins of Complex Multicellularity (2011, background): “Signaling by reactive oxygen species, already introduced in association with life-cycle differentiation among protists, finds use in both plant (Foyer & Noctor 2005) and animal (Fisher & Burggren 2007) development.”
Prospects of Halophytes in Understanding and Managing Abiotic Stress Tolerance (2012, background): “The concept of a cellular redox state, as proposed by Foyer and Noctor ( 2005 ) , is very useful in terms of elucidating the importance of redox reactions in gene expression, metabolism control, signal transduction, and cellular defense.”
Reactive oxygen species as universal constraints in life-history evolution (2009, background): “For instance, in plants, ROS are used to facilitate an array of essential biological processes (Apel & Hirt 2004; Foyer & Noctor 2005; Gechev et al. 2006), including immune defence (Apel & Hirt 2004), growth and development (Gapper & Dolan 2006; Gechev et al. 2006), seed germination (Schopfer et…”
Exogenous nitric oxide (NO) ameliorates salinity-induced oxidative stress in tomato (Solanum lycopersicum) plants (2014, background): “reductase (MDAR) and glutathione reductase (GR), as well as glutathione (GSH) and ascorbate, are also important components of the ascorbate-glutathione cycle responsible for the removal of H2O2 in different cellular compartments (Foyer and Noctor, 2005).”
Silicon alleviates cadmium toxicity in peanut plants in relation to cadmium distribution and stimulation of antioxidative enzymes (2010, background): “generate ROS directly, it generates oxidative stress via interference with the antioxidant defense system ( Foyer and Noctor 2005 ), and promote MDA content in plants due to increased lipid peroxidation (Krantev et al. 2008).”
Exogenous glutathione attenuates lead-induced oxidative stress in wheat by improving antioxidant defense and physiological mechanisms (2018, background): “In a plant cell, GSH is major non-protein thiol component which is water-soluble antioxidant having multifarious biochemical roles in plant stress adaptation (Foyer and Noctor 2005a, 2005b).”
Glutathione in plants: biosynthesis and physiological role in environmental stress tolerance (2017, positive): “The following is a discussion of some feasible proposed pathways: Under different abiotic stress conditions, GSH (either alone or with H2O2 or some other ROS) triggers adaptive or cell death processes through an intercellular signaling system (Foyer and Noctor 2005a, b).”