Effects of shear stress on eicosanoid gene expression and metabolite production in vascular endothelium as studied in a novel biomechanical perfusion model

Biochem Biophys Res Commun. 2000 Mar 5;269(1):257-64. doi: 10.1006/bbrc.2000.2279.

Abstract

This study investigated the effects of shear stress on gene expression of prostacyclin synthesis-related enzymes cyclooxygenases (COX-1 and COX-2), prostacyclin synthase (PGS), and thromboxane synthase (TXS) and their metabolites prostaglandin (PGI(2)) and thromboxane A(2) (TXA(2)) in endothelium of intact conduit vessels. Paired human umbilical veins were perfused at high/low shear stress (25/<4 dyn/cm(2)) at identical intraluminal pressure (20 mmHg) for 1.5, 3, or 6 hours in a computerized vascular model. High shear perfusion induced a significant, monophasic upregulation of PGS and TXS gene expressions after 6 hours. COX-1 and COX-2 mRNA showed a biphasic response with peaks at 1.5 and 6 hours, with a nadir level at 3 hours. Shear-induced gene expression was associated with a significantly greater accumulation of 6-keto prostaglandin F(1alpha) and TXA(2) in the perfusion medium. Thus, shear stress independently of perfusion pressure alters the expression of prostacyclin synthesis-related enzymes and the biosynthesis of their vasoactive metabolites.

MeSH terms

  • 6-Ketoprostaglandin F1 alpha / metabolism
  • Base Sequence
  • Biomechanical Phenomena
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • DNA Primers / genetics
  • Eicosanoids / genetics*
  • Eicosanoids / metabolism*
  • Endothelium, Vascular / metabolism*
  • Epoprostenol / metabolism
  • Female
  • Gene Expression
  • Humans
  • In Vitro Techniques
  • Isoenzymes / genetics
  • Membrane Proteins
  • Models, Cardiovascular
  • Perfusion
  • Pregnancy
  • Prostaglandin-Endoperoxide Synthases / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Stress, Mechanical
  • Thromboxane A2 / metabolism
  • Thromboxane-A Synthase / genetics
  • Umbilical Veins / metabolism

Substances

  • DNA Primers
  • Eicosanoids
  • Isoenzymes
  • Membrane Proteins
  • RNA, Messenger
  • Thromboxane A2
  • 6-Ketoprostaglandin F1 alpha
  • Epoprostenol
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Thromboxane-A Synthase