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Updated: Jan 26, 2026

Receptor Autoradiography Protocol for the Localized Visualization of Angiotensin II Receptors
Published on: June 7, 2016
Mitochondrial angiotensin receptors and cardioprotective pathways
Nelson Escobales1, Rebeca E Nuñez1, Sabzali Javadov1
1Department of Physiology, University of Puerto Rico School of Medicine , San Juan, Puerto Rico.
Abstract:
A growing body of data provides strong evidence that intracellular angiotensin II (ANG II) plays an important role in mammalian cell function and is involved in the pathogenesis of human diseases such as hypertension, diabetes, inflammation, fibrosis, arrhythmias, and kidney disease, among others. Recent studies also suggest that intracellular ANG II exerts protective effects in cells during high extracellular levels of the hormone or during chronic stimulation of the local tissue renin-angiotensin system (RAS). Notably, the intracellular RAS (iRAS) described in neurons, fibroblasts, renal cells, and cardiomyocytes provided new insights into regulatory mechanisms mediated by intracellular ANG II type 1 (AT1Rs) and 2 (AT2Rs) receptors, particularly, in mitochondria and nucleus. For instance, ANG II through nuclear AT1Rs promotes protective mechanisms by stimulating the AT2R signaling cascade, which involves mitochondrial AT2Rs and Mas receptors. The stimulation of nuclear ANG II receptors enhances mitochondrial biogenesis through peroxisome proliferator-activated receptor-γ coactivator-1α and increases sirtuins activity, thus protecting the cell against oxidative stress. Recent studies in ANG II-induced preconditioning suggest that plasma membrane AT2R stimulation exerts protective effects against cardiac ischemia-reperfusion by modulating mitochondrial AT1R and AT2R signaling. These studies indicate that iRAS promotes the protection of cells through nuclear AT1R signaling, which, in turn, promotes AT2R-dependent processes in mitochondria. Thus, despite abundant data on the deleterious effects of intracellular ANG II, a growing body of studies also supports a protective role for iRAS that could be of relevance to developing new therapeutic strategies. This review summarizes and discusses previous studies on the role of iRAS, particularly emphasizing the protective and counterbalancing actions of iRAS, mitochondrial ANG II receptors, and their implications for organ protection.
Insights
Intracellular angiotensin II (ANG II) has dual roles, contributing to diseases and offering cellular protection via the intracellular renin-angiotensin system (iRAS). The iRAS, particularly nuclear and mitochondrial receptors, promotes organ protection against oxidative stress.
Area of Science:
- Cellular biology
- Cardiovascular research
- Renal physiology
Background:
- Intracellular angiotensin II (ANG II) is implicated in various human diseases, including hypertension and kidney disease.
- Emerging evidence highlights protective roles of intracellular ANG II, especially under stress conditions.
Purpose of the Study:
- To review the dual role of intracellular ANG II, focusing on its protective functions.
- To elucidate the mechanisms of the intracellular renin-angiotensin system (iRAS), particularly involving nuclear and mitochondrial receptors.
Main Methods:
- Review of existing literature on intracellular ANG II and iRAS.
- Analysis of studies investigating ANG II type 1 (AT1R) and type 2 (AT2R) receptors in cellular compartments.
- Examination of signaling pathways involving Mas receptors, PGC-1α, and sirtuins.
Main Results:
- Intracellular ANG II, via nuclear AT1Rs, can activate protective AT2R signaling cascades.
- Nuclear and mitochondrial AT2R stimulation enhances mitochondrial biogenesis and sirtuin activity, combating oxidative stress.
- Plasma membrane AT2R stimulation shows protective effects against cardiac ischemia-reperfusion injury.
Conclusions:
- The intracellular renin-angiotensin system (iRAS) plays a significant protective role in cells, counterbalancing deleterious effects of ANG II.
- Targeting iRAS, particularly mitochondrial and nuclear receptors, offers potential therapeutic strategies for organ protection.
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