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Signaling Components of Redox Active Endosomes: The Redoxosomes

Authors :
Qiang Li
Duane Abbott
Fredrick D. Oakley
John F. Engelhardt
Source :
Antioxidants & Redox Signaling. 11:1313-1333
Publication Year :
2009
Publisher :
Mary Ann Liebert Inc, 2009.

Abstract

Subcellular compartmentalization of reactive oxygen species (ROS) plays a critical role in transmitting cell signals in response to environmental stimuli. In this regard, signals at the plasma membrane have been shown to trigger NADPH oxidase-dependent ROS production within the endosomal compartment and this step can be required for redox-dependent signal transduction. Unique features of redox-active signaling endosomes can include NADPH oxidase complex components (Nox1, Noxo1, Noxa1, Nox2, p47phox, p67phox, and/or Rac1), ROS processing enzymes (SOD1 and/or peroxiredoxins), chloride channels capable of mediating superoxide transport and/or membrane gradients required for Nox activity, and novel redox-dependent sensors that control Nox activity. This review will discuss the cytokine and growth factor receptors that likely mediate signaling through redox-active endosomes, and the common mechanisms whereby they act. Additionally, the review will cover ligand-independent environmental injuries, such as hypoxia/reoxygenation injury, that also appear to facilitate cell signaling through NADPH oxidase at the level of the endosome. We suggest that redox-active endosomes encompass a subset of signaling endosomes that we have termed redoxosomes. Redoxosomes are uniquely equipped with redox-processing proteins capable of transmitting ROS signals from the endosome interior to redox-sensitive effectors on the endosomal surface. In this manner, redoxosomes can control redox-dependent effector functions through the spatial and temporal regulation of ROS as second messengers. Antioxid. Redox Signal. 11, 1313–1333.

Details

ISSN :
15577716 and 15230864
Volume :
11
Database :
OpenAIRE
Journal :
Antioxidants & Redox Signaling
Accession number :
edsair.doi.dedup.....d0209025127e987afce92531d6746047
Full Text :
https://doi.org/10.1089/ars.2008.2363