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Angiotensin II, NADPH oxidase, and redox signaling in the vasculature.

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TLDR
There is still a paucity of information on how Ang II exerts cell-specific effects through ROS and how Nox isoforms are differentially regulated by Ang II, and exact mechanisms whereby ROS induce oxidative modifications of signaling molecules mediating Ang II actions remain elusive.
Abstract
Significance: Angiotensin II (Ang II) influences the function of many cell types and regulates many organ systems, in large part through redox-sensitive processes. In the vascular system, Ang II is a potent vasoconstrictor and also promotes inflammation, hypertrophy, and fibrosis, which are important in vascular damage and remodeling in cardiovascular diseases. The diverse actions of Ang II are mediated via Ang II type 1 and Ang II type 2 receptors, which couple to various signaling molecules, including NADPH oxidase (Nox), which generates reactive oxygen species (ROS). ROS are now recognized as signaling molecules, critically placed in pathways activated by Ang II. Mechanisms linking Nox and Ang II are complex and not fully understood. Recent Advances: Ang II regulates vascular cell production of ROS through various recently characterized Noxs, including Nox1, Nox2, Nox4, and Nox5. Activation of these Noxs leads to ROS generation, which in turn influences many downstream signaling targets of Ang II, including MAP kinases, RhoA/Rho kinase, transcription factors, protein tyrosine phosphatases, and tyrosine kinases. Activation of these redox-sensitive pathways regulates vascular cell growth, inflammation, contraction, and senescence. Critical Issues: Although there is much evidence indicating a role for Nox/ROS in Ang II function, there is still a paucity of information on how Ang II exerts cell-specific effects through ROS and how Nox isoforms are differentially regulated by Ang II. Moreover, exact mechanisms whereby ROS induce oxidative modifications of signaling molecules mediating Ang II actions remain elusive. Future Directions: Future research should elucidate these issues to better understand the significance of Ang II and ROS in vascular (patho) biology. Antioxid. Redox Signal. 19, 1110–1120.

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References
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Journal ArticleDOI

Role of Renin-Angiotensin System in Inflammation, Immunity and Aging

TL;DR: The present review updates the novel roles of classical and new RAS components and their possible implication during the physiological aging, in the immune system and inflammation, and some studies suggest a new potential application of RAS blockers in autoimmune diseases.
Journal ArticleDOI

Redox-dependent MAP kinase signaling by Ang II in vascular smooth muscle cells: role of receptor tyrosine kinase transactivation.

TL;DR: It is suggested that Ang II activates p38MAP kinase and ERK5 via redox-dependent cascades that are regulated by IGF-1R and EGFR transactivation, which suggests that ERK1/2 regulation by Ang II is viaRedox-insensitive pathways.
Journal ArticleDOI

Pathophysiological regulation of the At1-receptor and implications for vascular disease

TL;DR: Treatment with AT1-receptor blockers may inhibit the onset and progression of vascular oxidative stress and inflammation, endothelial dysfunction, atherosclerosis, and related organ damage.
Journal ArticleDOI

Redox regulation of protein kinases as a modulator of vascular function.

TL;DR: The molecular mechanisms of redox modification of protein kinases, the downstream pathways affected, the often complex interaction between major kinase pathways, and feedback to ROS production itself are discussed.
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