Hydraulic conductance of pulmonary microvascular and macrovascular endothelial cell monolayers

Am J Physiol Lung Cell Mol Physiol. 2006 Jul;291(1):L30-7. doi: 10.1152/ajplung.00317.2005.

Abstract

Endothelial cells isolated from pulmonary arteries (RPAEC) and microcirculation (RPMVEC) of rat lungs were grown to confluence on porous filters and mounted on an Ussing-type chamber. Transmembrane pressure (deltaP) was controlled by the reservoir height, and the filtration rate corrected for surface area (J(v)/A) was measured by timing fluid movement in a calibrated micropipette. These parameters were used to calculate hydraulic conductance (Lp) by using linear regression of J(v)/A on deltaP. Mean Lp values for newly confluent RPAEC monolayers were 22 times higher than those for RPMVEC monolayers (28.6 +/- 5.6 vs. 1.30 +/- 0.50 x 10(-7) cm x s(-1) x cmH2O(-1); P < or = 0.01). After confluence was reached, electrical resistance and Lp remained stable in RPAEC but continued to change in RPMVEC with days in culture. Both phenotypes exhibited an initial time-dependent sealing response, but Lp also had an inverse relationship to deltaP in RPMVEC monolayers > or = 4 days postconfluence that was attributed to cell overgrowth rather than junctional length. In a comparison of the cadherin contents, E-cadherin was predominant in RPMVEC, but VE-cadherin was predominant in RPAEC. At a constant deltaP of 40-45 cmH2O for 2 h, J(v)/A increased 225% in RPAEC monolayers but did not change significantly in RPMVEC monolayers. Significant decreases in Lp were obtained after treatment with 5% albumin, GdCl3, or isoproterenol plus rolipram in both phenotypes. Thus lung microvascular endothelial cells exhibited a significantly lower Lp than conduit vessel endothelium, which would limit alveolar flooding relative to perivascular edema cuff formation during increased pulmonary vascular pressures.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Albumins / pharmacology
  • Animals
  • Antigens, CD
  • Cadherins / metabolism
  • Capillary Permeability / drug effects
  • Capillary Permeability / physiology*
  • Cells, Cultured
  • Endothelial Cells / metabolism*
  • Endothelial Cells / ultrastructure
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism*
  • Filtration
  • Gadolinium / pharmacology
  • Gap Junctions / metabolism
  • Gap Junctions / ultrastructure
  • Isoproterenol / pharmacology
  • Lung / blood supply*
  • Microscopy, Electron
  • Phosphodiesterase Inhibitors / pharmacology
  • Pressure
  • Pulmonary Edema / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Rolipram / pharmacology

Substances

  • Adrenergic beta-Agonists
  • Albumins
  • Antigens, CD
  • Cadherins
  • Phosphodiesterase Inhibitors
  • cadherin 5
  • Gadolinium
  • Rolipram
  • Isoproterenol