New tricks from an old dog: mitochondrial redox signaling in cellular inflammation.

TitleNew tricks from an old dog: mitochondrial redox signaling in cellular inflammation.
Publication TypeJournal Article
Year of Publication2012
AuthorsPelletier, M, Lepow, TS, Billingham, LK, Murphy, MP, Siegel, RM
JournalSemin Immunol
Volume24
Issue6
Pagination384-92
Date Published2012 Dec
ISSN1096-3618
KeywordsCell Communication, Humans, Immune System, Inflammation, Mitochondria, Oxidation-Reduction, Reactive Oxygen Species, Signal Transduction
Abstract

Reactive oxygen species (ROS) such as superoxide (O(2)(-)) and hydrogen peroxide (H(2)O(2)) have long been implicated as pro-inflammatory, yet the sources of ROS and the molecular mechanisms by which they enhance inflammation have been less clear. Recent advances in the understanding of the molecular basis of inflammation mediated by the innate immune system have allowed these issues to be revisited. Although the Nox2 NADPH oxidases generate the bulk of ROS for antimicrobial host defense, recent studies have found that NADPH oxidase-dependent ROS production can actually dampen macrophage inflammatory responses to sterile pro-inflammatory stimuli. Instead, production of mitochondrial ROS has emerged as an important factor in both host defense and sterile inflammation. Excess mitochondrial ROS can be generated by either damage to the respiratory chain or by alterations of mitochondrial function such as those that increase membrane potential and reduce respiratory electron carriers. In autoinflammatory diseases, where key components of innate immune responses are activated by genetic mutations or environmental stimuli, inflammation has been found to be particularly sensitive to inhibition of mitochondrial ROS production. These findings have highlighted mitochondrial ROS as a novel generator of pro-inflammatory ROS and a potential therapeutic target in inflammatory diseases.

DOI10.1016/j.smim.2013.01.002
Alternate JournalSemin. Immunol.
Citation Key10.1016/j.smim.2013.01.002
PubMed ID23391428
PubMed Central IDPMC3650900
Grant ListMC_U105663142 / / Medical Research Council / United Kingdom
Z01 AR041175-01 / / Intramural NIH HHS / United States
/ / Medical Research Council / United Kingdom