AT2 receptor stimulation inhibits phosphate-induced vascular calcification

Masayoshi Kukida1, Masaki Mogi2, Harumi Kan-No2

  • 1Department of Molecular Cardiovascular Biology and Pharmacology, Ehime University, Graduate School of Medicine, Tohon, Japan; Department of Cardiology, Pulmonology, Hypertension and Nephrology, Ehime University, Graduate School of Medicine, Tohon, Japan.

Kidney International
|November 17, 2018
PubMed

Insights

Angiotensin II type 2 receptor (AT2) stimulation inhibits phosphate-induced vascular calcification. This protective effect, mediated partly by PPAR-γ, may reduce cardiovascular events in chronic kidney disease patients.

Area of Science:

  • Cardiovascular Biology
  • Renal Medicine
  • Molecular Pharmacology

Background:

  • Vascular calcification is prevalent in atherosclerosis and chronic kidney disease.
  • The renin-angiotensin system influences cardiovascular remodeling.
  • The role of angiotensin II type 2 receptor (AT2) in vascular calcification is unclear.

Purpose of the Study:

  • To investigate the hypothesis that AT2 receptor stimulation inhibits phosphate-induced vascular calcification.
  • To explore the underlying molecular mechanisms, including the role of PPAR-γ.

Main Methods:

  • In vivo studies using adenine and high-phosphate diet in smooth muscle cell-specific AT2-overexpressing (smAT2-Tg) mice, wild-type, and AT2-knockout (AT2KO) mice.
  • Ex vivo culture of thoracic aorta rings.
  • In vitro studies using primary vascular smooth muscle cells.
  • Assessment of osteogenic and vascular smooth muscle cell marker gene expression.
  • Investigation of PPAR-γ involvement using a specific antagonist.

Main Results:

  • smAT2-Tg mice exhibited significantly attenuated thoracic aorta calcification compared to wild-type and AT2KO mice.
  • Gene expression of osteogenic and vascular smooth muscle cell markers remained unchanged in smAT2-Tg mice but altered in wild-type mice.
  • Ex vivo and in vitro studies confirmed reduced calcification in smAT2-Tg derived tissues and cells.
  • PPAR-γ antagonism diminished the protective effect of AT2 stimulation against vascular calcification.

Conclusions:

  • AT2 receptor activation is an endogenous protective pathway against vascular calcification.
  • AT2 stimulation, potentially via PPAR-γ, can inhibit phosphate-induced vascular calcification.
  • Targeting AT2 activation may offer a therapeutic strategy to reduce cardiovascular events in chronic kidney disease.

Related Concept Videos

Feedback Inhibition00:46

Feedback Inhibition

Biochemical reactions are occurring constantly in cells, converting starting substances to different products, usually with the help of enzymes that speed the reactions. Without enzymes, it would take far too long for most reactions to occur to be useful to the cell!
57.1K
Receptor-mediated Endocytosis01:39

Receptor-mediated Endocytosis

Overview
110.9K
Phosphate Buffer01:22

Phosphate Buffer

The phosphate buffer system is a critical biological mechanism for maintaining pH stability in the body. This system operates primarily through two components: sodium dihydrogen phosphate (NaH2PO4), which acts as a weak acid, and sodium hydrogen phosphate (Na2HPO4), which serves as a weak base.
Sodium dihydrogen phosphate does not fully dissociate in neutral or acidic solutions. When a strong base, such as sodium hydroxide (NaOH), is introduced into the solution, sodium dihydrogen phosphate...
5.2K
Enzyme-linked Receptors01:00

Enzyme-linked Receptors

Enzyme-linked receptors are proteins that act as both receptor and enzyme, activating multiple intracellular signals. This is a large group of receptors that include the receptor tyrosine kinase (RTK) family. Many growth factors and hormones bind to and activate the RTKs.
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
86.6K
Internal Receptors01:31

Internal Receptors

Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
74.7K
Seedless Vascular Plants03:24

Seedless Vascular Plants

Seedless Vascular Plants Were the First Tall Plants on Earth
66.9K