scispace - formally typeset
Open AccessJournal ArticleDOI

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

Reads0
Chats0
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.

read more

Citations
More filters
Journal ArticleDOI

PGC-1α limits angiotensin II-induced rat vascular smooth muscle cells proliferation via attenuating NOX1-mediated generation of reactive oxygen species.

TL;DR: The protein content of PGC-1α was negatively correlated with an increase in cell proliferation and migration induced by AngII and could decrease ROS generation derived from NADPH oxidase induced byAngII, thus attenuating VSMC hyperplasia.

Matrix vesicles induce calcification of recipient vascular smooth muscle cells through multiple signaling pathways

TL;DR: Adding cellular-derived matrix vesicles from calcifying VSMC can accelerate calcification by inducing cell signaling changes and phenotypic alteration of recipient VSMC, suggesting a potential therapeutic role of such inhibition.
Journal ArticleDOI

SARS-CoV-2 infection and oxidative stress: Pathophysiological insight into thrombosis and therapeutic opportunities

TL;DR: In this paper, the authors survey the mechanisms of how severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces oxidative stress and the consequences of this stress on patient health.
Journal ArticleDOI

Role of Oxidative Stress in the Genesis of Ventricular Arrhythmias

TL;DR: It is concluded that pharmacological approaches targeting multiple mechanisms besides oxidative stress might be more effective in the treatment of ventricular arrhythmias than current antiarrhythmic therapy.
Journal ArticleDOI

c-Src Inhibition Improves Cardiovascular Function but not Remodeling or Fibrosis in Angiotensin II-Induced Hypertension

TL;DR: The data indicate that although c-Src downregulation attenuates development of hypertension, improves endothelial and cardiac function, reduces oxidative stress, and normalizes vascular signaling, it has little beneficial effect on fibrosis.
References
More filters
Journal ArticleDOI

Angiotensin II stimulates NADH and NADPH oxidase activity in cultured vascular smooth muscle cells.

TL;DR: The ability of Ang II to stimulate superoxide anion formation is examined and the identity of the oxidases responsible for its production is investigated to suggest that Ang II specifically activates enzyme systems that promote superoxide generation and raise the possibility that these pathways function as second messengers for long-term responses, such as hypertrophy or hyperplasia.
Journal ArticleDOI

Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NADH/NADPH oxidase activation. Contribution to alterations of vasomotor tone.

TL;DR: Forms of hypertension associated with elevated circulating levels of angiotensin II may have unique vascular effects not shared by other forms of hypertension because they increase vascular smooth muscle .O2- production via NADH/NADPH oxidase activation.
Journal ArticleDOI

Angiotensin II cell signaling: physiological and pathological effects in the cardiovascular system

TL;DR: This review focuses on the structure and function of AT(1) receptors and the major signaling mechanisms by which angiotensin influences cardiovascular physiology and pathology.
Journal ArticleDOI

Superoxide anion radical (O2-.), superoxide dismutases, and related matters.

TL;DR: This review will describe only aspects of the biology of oxygen radicals that currently engage the interest of the writer and Hopefully they will also be of interest to the reader.
Journal ArticleDOI

Vascular NAD(P)H oxidases: specific features, expression, and regulation

TL;DR: Members of this enzyme family appear to be important in vascular biology and disease and constitute promising targets for future therapeutic interventions.
Related Papers (5)