Phosphorylation of caveolin-1 regulates oxidant-induced pulmonary vascular permeability via paracellular and transcellular pathways

Circ Res. 2009 Sep 25;105(7):676-85, 15 p following 685. doi: 10.1161/CIRCRESAHA.109.201673. Epub 2009 Aug 27.

Abstract

Rationale: Oxidants are important signaling molecules known to increase endothelial permeability, although the mechanisms underlying permeability regulation are not clear.

Objective: To define the role of caveolin-1 in the mechanism of oxidant-induced pulmonary vascular hyperpermeability and edema formation.

Methods and results: Using genetic approaches, we show that phosphorylation of caveolin-1 Tyr14 is required for increased pulmonary microvessel permeability induced by hydrogen peroxide (H(2)O(2)). Caveolin-1-deficient mice (cav-1(-/-)) were resistant to H(2)O(2)-induced pulmonary vascular albumin hyperpermeability and edema formation. Furthermore, the vascular hyperpermeability response to H(2)O(2) was completely rescued by expression of caveolin-1 in cav-1(-/-) mouse lung microvessels but was not restored by the phosphorylation-defective caveolin-1 mutant. The increase in caveolin-1 phosphorylation induced by H(2)O(2) was dose-dependently coupled to both increased (125)I-albumin transcytosis and decreased transendothelial electric resistance in pulmonary endothelial cells. Phosphorylation of caveolin-1 following H(2)O(2) exposure resulted in the dissociation of vascular endothelial cadherin/beta-catenin complexes and resultant endothelial barrier disruption.

Conclusions: Caveolin-1 phosphorylation-dependent signaling plays a crucial role in oxidative stress-induced pulmonary vascular hyperpermeability via transcellular and paracellular pathways. Thus, caveolin-1 phosphorylation may be an important therapeutic target for limiting oxidant-mediated vascular hyperpermeability, protein-rich edema formation, and acute lung injury.

Publication types

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

MeSH terms

  • Albumins / metabolism
  • Animals
  • Antigens, CD / metabolism
  • Cadherins / metabolism
  • Capillary Permeability / drug effects*
  • Caveolin 1 / deficiency
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Endocytosis
  • Endothelial Cells / drug effects*
  • Endothelial Cells / metabolism
  • Hydrogen Peroxide / toxicity*
  • Intercellular Junctions / metabolism
  • Lung / blood supply*
  • Mice
  • Mice, Knockout
  • Microvessels / drug effects
  • Microvessels / metabolism
  • Oxidants / toxicity*
  • Oxidative Stress / drug effects*
  • Phosphorylation
  • Proto-Oncogene Proteins c-abl / metabolism
  • Pulmonary Edema / metabolism
  • Pulmonary Edema / prevention & control
  • Rats
  • Signal Transduction / drug effects
  • Time Factors
  • Tyrosine
  • beta Catenin / metabolism
  • src-Family Kinases / metabolism

Substances

  • Albumins
  • Antigens, CD
  • Cadherins
  • Cav1 protein, mouse
  • Cav1 protein, rat
  • Caveolin 1
  • Ctnnb1 protein, rat
  • Oxidants
  • beta Catenin
  • cadherin 5
  • Tyrosine
  • Hydrogen Peroxide
  • Proto-Oncogene Proteins c-abl
  • src-Family Kinases