Basic Research in Cardiology

, Volume 94, Issue 5, pp 322–332

Effect of HMG-CoA reductase inhibitors on extracellular matrix expression in human vascular smooth muscle cells

  • R. Riessen
  • D. I. Axel
  • M. Fenchel
  • U. U. Herzog
  • H. Roßmann
  • K. R. Karsch
Original Contribution

DOI: 10.1007/s003950050158

Cite this article as:
Riessen, R., Axel, D., Fenchel, M. et al. Basic Res Cardiol (1999) 94: 322. doi:10.1007/s003950050158

Abstract

Clinical studies have shown that treatment with 3-hydroxy-3-methyl-glutaryl-coenzyme A (HMG-CoA) reductase inhibitors can stabilize atherosclerotic plaques and slow their progression. One determinant of plaque stability and size is the composition of the vascular extracellular matrix. The aim of this study was to evaluate the effects of different HMG-CoA reductase inhibitors on the expression of major components of the vascular extracellular matrix in smooth muscle cells.

Cultured human vascular smooth muscle cells were incubated for 24–72 h with the HMG-CoA reductase inhibitors lovastatin (1–50 μmol/L), simvastatin (0.05–20 μmol/L), and pravastatin ( 1–100 μmol/L). RNA expression of the extracellular matrix proteins thrombospondin-1, fibronectin, collagen type I, and biglycan as well as expression of the cytokine TGF-β1 was determined by Northern blotting. Extracellular matrix protein secretion was visualized by immunofluorescence. In addition, cell proliferation and viability were measured using BrDU-ELISAs, MTT-tests, and direct cell counting.

Expression of thrombospondin-1 was significantly decreased after 24 h incubations with lovastatin in concentrations as low as 1 μmol/L. Coincubation with the cholesterol precursor mevalonate completely reversed this effect. The downregulation of thrombospondin-1 expression occured in the same concentration range that also inhibited cell proliferation. In contrast, lovatatin did not affect expression of fibronectin, whereas collagen type I and biglycan expression decreased only after long incubations with high, toxic lovastatin concentrations. Simvastatin, but not the very hydrophilic compound pravastatin, had a similar effect on extracellular matrix expression as lovastatin.

In summary, lovastatin and simvastatin predominantly decrease the expression of the glycoprotein thrombospondin-1, which is functionally associated with smooth muscle cell migration and proliferation. In contrast, expression of plaque-stabilizing extracellular proteins such as collagen type I and biglycan are much less affected.

Key words Atherosclerosis – extracellular matrix – HMG-CoA reductase inhibitors – smooth muscle – thrombospondin 

Copyright information

© Steinkopff Verlag 1999

Authors and Affiliations

  • R. Riessen
    • 1
  • D. I. Axel
    • 1
  • M. Fenchel
    • 1
  • U. U. Herzog
    • 1
  • H. Roßmann
    • 2
  • K. R. Karsch
    • 1
  1. 1.Department of Medicin III (Cardiology), University of Tübingen, Otfried-Müller-Str. 10, D-72076 Tübingen, E-mail: reimer.riessen@uni-tuebingen.deDE
  2. 2.Department of Medicine I, University of Tübingen, Otfried-Müller-Str. 10, D-72076 TübingenDE