Lipoprotein(a) enhances the expression of intercellular adhesion molecule-1 in cultured human umbilical vein endothelial cells

Circulation. 1998 Mar 3;97(8):721-8. doi: 10.1161/01.cir.97.8.721.

Abstract

Background: We reported an increase in serum lipoprotein(a) [Lp(a)] levels in patients with thromboangiitis obliterans, suggesting that Lp(a) could also contribute to the pathogenesis of cardiovascular diseases by a mechanism different from atherosclerosis. Adhesion molecules were shown to contribute to the development of not only atherosclerotic but also inflammatory vascular diseases.

Methods and results: We evaluated the effect of Lp(a) on the expression of intercellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1, and E-selectin in human umbilical vein endothelial cells by a cell ELISA. Lp(a) dramatically enhanced the levels of ICAM-1 in a dose-dependent manner. A discernible increase in ICAM-1 expression was observed at a physiological concentration of 0.26 mmol cholesterol/L Lp(a) after 48-hour incubation. A 1.8-fold increase in ICAM-1 expression was observed 48 hours after the addition of Lp(a) (1.04 mmol cholesterol/L). Northern blot analysis demonstrated that the amount of ICAM-1 mRNA was increased after treatment with Lp(a). In contrast to ICAM-1, the expression of VCAM-1 and E-selectin was not significantly affected by Lp(a). Lp(a-) [apolipoprotein(a)- removed Lp(a) by reduction with dithiothreitol] and LDL had no significant effect on the expression of ICAM-1. In contrast, recombinant apolipoprotein(a) protein alone significantly enhanced ICAM-1 expression. Lp(a) decreased the level of active transforming growth factor (TGF)-beta in the conditioned medium. Furthermore, recombinant TGF-beta significantly decreased the Lp(a)-induced ICAM-1 expression. These findings suggested that Lp(a) may enhance the ICAM-1 expression by decreasing active TGF-beta level.

Conclusions: Lp(a) could contribute to the development of cardiovascular diseases by enhancing the expression of ICAM-1 in endothelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / immunology
  • Antibodies / pharmacology
  • Apolipoproteins A / pharmacology
  • Blotting, Northern
  • Cell Line
  • Culture Media, Conditioned / chemistry
  • Culture Media, Conditioned / metabolism
  • E-Selectin / drug effects
  • E-Selectin / genetics
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / metabolism
  • Gene Expression / drug effects
  • Gene Expression / genetics
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / genetics
  • Humans
  • Intercellular Adhesion Molecule-1 / drug effects*
  • Intercellular Adhesion Molecule-1 / genetics*
  • Lipoprotein(a) / pharmacology*
  • Lipoproteins / pharmacology
  • Lipoproteins, LDL / pharmacology
  • Neutralization Tests
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism
  • Recombinant Proteins / pharmacology
  • Transforming Growth Factor beta / drug effects
  • Transforming Growth Factor beta / immunology
  • Transforming Growth Factor beta / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology
  • Umbilical Veins / cytology
  • Up-Regulation / immunology

Substances

  • Antibodies
  • Apolipoproteins A
  • Culture Media, Conditioned
  • E-Selectin
  • Lipoprotein(a)
  • Lipoproteins
  • Lipoproteins, LDL
  • RNA, Messenger
  • Recombinant Proteins
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1