IMR Press / FBL / Volume 8 / Issue 4 / DOI: 10.2741/999

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on as a courtesy and upon agreement with Frontiers in Bioscience.

Open Access Article
Mitogen-activated protein kinase pathways in redox signaling
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1 Childrens Hospital Los Angeles Research Institute, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, CA 90027, USA

Academic Editor: Ramesh Natarajan

Front. Biosci. (Landmark Ed) 2003, 8(4), 369–391;
Published: 1 January 2003
(This article belongs to the Special Issue Nitric oxide and ROS mediated signaling)

It has been known for quite some time that proper cellular function requires tight control of the cellular redox state. In recent years, a growing body of literature has provided evidence of a role for reactive oxygen species (ROS) as important mediators of proliferation, acting as second messengers to modulate the activation of various signaling molecules and pathways. In contrast to high levels of ROS that may induce modifications that inhibit the activity of cellular components or result in damage, repair and cell death, the hypothesis that low levels of ROS, produced enzymatically and in a regulated fashion, are required participants of signaling pathways controlling essential cellular function is gaining grounds. The concept that ROS specifically target components of these pathways is only beginning to be examined. The mitogen-activated protein kinases (MAPK) are a large family of proline-directed, serine/threonine kinases that require tyrosine and threonine phosphorylation of a ThrXTyr motif in the activation loop for activation. Receptor-ligand interaction leads to activation of a phosphorylation cascade where the minimal module is formed by MAPK, MAPK kinase and MAPK kinase kinase. Four separate MAPK and activating cascades have been identified, based on the TXY motif and the dual-specificity kinases that strictly phosphorylate their particular TXY sequence. They are the extracellular signal regulated kinases (ERK), c-jun N-terminal kinases (JNK), p38MAPK and ERK5. This review will summarize recent findings regarding the activation of the MAPK and the role played by ROS in their activation.

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