Endothelial cells modulate smooth muscle cell morphology by inhibition of transforming growth factor-beta 1 activation

Surgery. 1996 Aug;120(2):418-25; discussion 425-6. doi: 10.1016/s0039-6060(96)80318-7.

Abstract

Background: We have previously demonstrated in a coculture model that endothelial cells (ECs) exert regulatory control over smooth muscle cell (SMC) morphology. This study was performed to test the hypothesis that ECs inhibit transforming growth factor-beta 2 (TGF-beta 1) activation through the release of plasminogen activator inhibitor (PAI-1).

Methods: Bovine SMCs were cultured on a thin, semipermeable membrane, either alone or opposite ECs in coculture (SMC/EC). Conditioned media and cell lysates at 1, 5, and 21 days were assayed for TGF-beta 1 and PAI-1 by enzyme-linked immunoabsorbent assay. Cell proliferation rates, protein, and DNA content were measured and compared with SMC morphology.

Results: Activation of TGF-beta 1 was significantly decreased (1.2% versus 18.9% active TGF-beta 1 p < 0.05) and PAI-1 was increased (659 pg/ml versus 343 pg/ml p < 0.05) in SMC/EC medium on day 1, compared with the medium of SMC alone. Significantly higher levels of PAI-1 were measured in cell lysates of cocultured ECs (128 pg/micrograms DNA) than in cocultured SMCs (5.8 pg/micrograms DNA, p < 0.05). SMC/EC coculture prevented the SMC hill-and-valley growth morphology seen in SMCs cultured alone.

Conclusions: In a model designed to study SMC/EC interactions, it was seen that ECs can alter growth characteristics of SMCs by producing PAI-1, which interferes with the plasminogen pathway of TGF-beta 1 activation. This suggests that reduced EC PAI-1 production could play a role in alteration of SMC phenotype in vivo.

MeSH terms

  • Animals
  • Aorta / cytology
  • Cattle
  • Cell Division / drug effects
  • Cell Size / physiology
  • Cells, Cultured / physiology
  • DNA / analysis
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / physiology*
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / physiology*
  • Plasminogen Activator Inhibitor 1 / metabolism
  • Proteins / analysis
  • Serine Proteinase Inhibitors / metabolism
  • Thymidine / metabolism
  • Transforming Growth Factor beta / antagonists & inhibitors*
  • Transforming Growth Factor beta / metabolism
  • Tritium / metabolism

Substances

  • Plasminogen Activator Inhibitor 1
  • Proteins
  • Serine Proteinase Inhibitors
  • Transforming Growth Factor beta
  • Tritium
  • DNA
  • Thymidine