Uncoupling Caveolae From Intracellular Signaling In Vivo

Circ Res. 2016 Jan 8;118(1):48-55. doi: 10.1161/CIRCRESAHA.115.307767. Epub 2015 Nov 24.

Abstract

Rationale: Caveolin-1 (Cav-1) negatively regulates endothelial nitric oxide (NO) synthase-derived NO production, and this has been mapped to several residues on Cav-1, including F92. Herein, we reasoned that endothelial expression of an F92ACav-1 transgene would let us decipher the mechanisms and relationships between caveolae structure and intracellular signaling.

Objective: This study was designed to separate caveolae formation from its downstream signaling effects.

Methods and results: An endothelial-specific doxycycline-regulated mouse model for the expression of Cav-1-F92A was developed. Blood pressure by telemetry and nitric oxide bioavailability by electron paramagnetic resonance and phosphorylation of vasodilator-stimulated phosphoprotein were determined. Caveolae integrity in the presence of Cav-1-F92A was measured by stabilization of caveolin-2, sucrose gradient, and electron microscopy. Histological analysis of heart and lung, echocardiography, and signaling were performed.

Conclusions: This study shows that mutant Cav-1-F92A forms caveolae structures similar to WT but leads to increases in NO bioavailability in vivo, thereby demonstrating that caveolae formation and downstream signaling events occur through independent mechanisms.

Keywords: caveolin-1; cell endothelial cell; eNOS; mice; nitric oxide; vascular function.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure / drug effects
  • Blood Pressure / physiology
  • Caveolae / drug effects
  • Caveolae / metabolism*
  • Caveolin 1 / biosynthesis*
  • Caveolin 1 / genetics*
  • Doxycycline / pharmacology
  • Humans
  • Intracellular Fluid / drug effects
  • Intracellular Fluid / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Nitric Oxide / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Uncoupling Agents / pharmacology

Substances

  • Cav1 protein, mouse
  • Caveolin 1
  • Uncoupling Agents
  • Nitric Oxide
  • Doxycycline