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Free Radic Biol Med. 2014 Nov;76:208-26. doi: 10.1016/j.freeradbiomed.2014.07.046. Epub 2014 Aug 23.

Nox family NADPH oxidases: Molecular mechanisms of activation.

Author information

1
Institut für Kardiovaskuläre Physiologie, Goethe-Universität Frankfurt, Frankfurt, Germany. Electronic address: r.brandes@em.uni-frankfurt.de.
2
ECCPS, Justus-Liebig-Universität, Member of the DZL, Giessen, Germany.
3
Institut für Kardiovaskuläre Physiologie, Goethe-Universität Frankfurt, Frankfurt, Germany.

Abstract

NADPH oxidases of the Nox family are important enzymatic sources of reactive oxygen species (ROS). Numerous homologue-specific mechanisms control the activity of this enzyme family involving calcium, free fatty acids, protein-protein interactions, intracellular trafficking, and posttranslational modifications such as phosphorylation, acetylation, or sumoylation. After a brief review on the classic pathways of Nox activation, this article will focus on novel mechanisms of homologue-specific activity control and on cell-specific aspects which govern Nox activity. From these findings of the recent years it must be concluded that the activity control of Nox enzymes is much more complex than anticipated. Moreover, depending on the cellular activity state, Nox enzymes are selectively activated or inactivated. The complex upstream signaling aspects of these events make the development of "intelligent" Nox inhibitors plausible, which selectively attenuate disease-related Nox-mediated ROS formation without altering physiological signaling ROS. This approach might be of relevance for Nox-mediated tissue injury in ischemia-reperfusion and inflammation and also for chronic Nox overactivation as present in cancer initiation and cardiovascular disease.

KEYWORDS:

Activity control; NADPH oxidase; Nox; Oxygen-derived free radicals; Phosphorylation; p22phox

[Indexed for MEDLINE]

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