Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling

PD Ray, BW Huang, Y Tsuji - Cellular signalling, 2012 - Elsevier
PD Ray, BW Huang, Y Tsuji
Cellular signalling, 2012Elsevier
Reactive oxygen species (ROS) are generated during mitochondrial oxidative metabolism
as well as in cellular response to xenobiotics, cytokines, and bacterial invasion. Oxidative
stress refers to the imbalance due to excess ROS or oxidants over the capability of the cell to
mount an effective antioxidant response. Oxidative stress results in macromolecular damage
and is implicated in various disease states such as atherosclerosis, diabetes, cancer,
neurodegeneration, and aging. Paradoxically, accumulating evidence indicates that ROS …
Reactive oxygen species (ROS) are generated during mitochondrial oxidative metabolism as well as in cellular response to xenobiotics, cytokines, and bacterial invasion. Oxidative stress refers to the imbalance due to excess ROS or oxidants over the capability of the cell to mount an effective antioxidant response. Oxidative stress results in macromolecular damage and is implicated in various disease states such as atherosclerosis, diabetes, cancer, neurodegeneration, and aging. Paradoxically, accumulating evidence indicates that ROS also serve as critical signaling molecules in cell proliferation and survival. While there is a large body of research demonstrating the general effect of oxidative stress on signaling pathways, less is known about the initial and direct regulation of signaling molecules by ROS, or what we term the “oxidative interface.” Cellular ROS sensing and metabolism are tightly regulated by a variety of proteins involved in the redox (reduction/oxidation) mechanism. This review focuses on the molecular mechanisms through which ROS directly interact with critical signaling molecules to initiate signaling in a broad variety of cellular processes, such as proliferation and survival (MAP kinases, PI3 kinase, PTEN, and protein tyrosine phosphatases), ROS homeostasis and antioxidant gene regulation (thioredoxin, peroxiredoxin, Ref-1, and Nrf-2), mitochondrial oxidative stress, apoptosis, and aging (p66Shc), iron homeostasis through iron–sulfur cluster proteins (IRE–IRP), and ATM-regulated DNA damage response.
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