Rapamycin, but not FK-506, increases endothelial tissue factor expression: implications for drug-eluting stent design

Circulation. 2005 Sep 27;112(13):2002-11. doi: 10.1161/CIRCULATIONAHA.105.569129. Epub 2005 Sep 19.

Abstract

Background: Drugs released from stents affect the biology of vascular cells. We examined the effect of rapamycin and FK-506 on tissue factor (TF) expression in human aortic endothelial cells (HAECs) and vascular smooth muscle cells (HAVSMCs).

Methods and results: Rapamycin enhanced thrombin- and tumor necrosis factor (TNF)-alpha-induced endothelial TF expression in a concentration-dependent manner. The maximal increase was 2.5-fold more pronounced than that by thrombin or TNF-alpha alone and was paralleled by a 1.4-fold higher TF surface activity compared with thrombin alone. Rapamycin by itself increased basal TF levels by 40%. In HAVSMCs, rapamycin did not affect thrombin- or TNF-alpha-induced TF expression. In contrast to rapamycin, FK-506 did not enhance thrombin- or TNF-alpha-induced endothelial TF expression. Thrombin induced a transient dephosphorylation of the mammalian target of rapamycin downstream target p70S6 kinase. Rapamycin completely abrogated p70S6 kinase phosphorylation, but FK-506 did not. FK-506 antagonized the effect of rapamycin on thrombin-induced TF expression. Rapamycin did not alter the pattern of p38, extracellular signal-regulated kinase, or c-Jun NH2-terminal kinase phosphorylation. Real-time polymerase chain reaction analysis revealed that rapamycin had no influence on thrombin-induced TF mRNA levels for up to 2 hours but led to an additional increase after 3 and 5 hours.

Conclusions: Rapamycin, but not FK-506, enhances TF expression in HAECs but not in HAVSMCs. This effect requires binding to FK binding protein-12, is mediated through inhibition of the mammalian target of rapamycin, and partly occurs at the posttranscriptional level. These findings may be clinically relevant for patients receiving drug-eluting stents, particularly when antithrombotic drugs are withdrawn or ineffective, and may open novel perspectives for the design of such stents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aorta
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Drug Delivery Systems
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Endothelium, Vascular / metabolism*
  • Equipment Design
  • Humans
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism
  • Myocytes, Smooth Muscle / cytology
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism
  • Protein Kinases / drug effects
  • RNA, Messenger / metabolism
  • Sirolimus / metabolism
  • Sirolimus / pharmacology*
  • Stents
  • TOR Serine-Threonine Kinases
  • Tacrolimus / pharmacology
  • Tacrolimus Binding Protein 1A / metabolism
  • Thromboplastin / genetics
  • Thromboplastin / metabolism*

Substances

  • RNA, Messenger
  • Thromboplastin
  • Protein Kinases
  • MTOR protein, human
  • TOR Serine-Threonine Kinases
  • Tacrolimus Binding Protein 1A
  • Sirolimus
  • Tacrolimus