Differential effect of wall tension on matrix metalloproteinase promoter activation in the thoracic aorta

J Surg Res. 2010 May 15;160(2):333-9. doi: 10.1016/j.jss.2008.12.033. Epub 2009 Jan 24.

Abstract

Background: Vascular remodeling relies upon extracellular matrix restructuring by the matrix metalloproteinases (MMPs). Induction of MMP-2 and MMP-9 by biological signaling molecules has been defined, but whether a mechanical stimulus such as elevated wall tension may generate MMP promoter activation remains unknown. Accordingly, this study examined whether MMP promoter activation would occur as a function of wall tension.

Materials and methods: The MMP-2 or MMP-9 promoter sequences were fused to the reporter gene lacZ and inserted into the mouse genome. Thoracic aortic rings were harvested (6 preparations/construct) and maintained under physiological conditions at predetermined tension values corresponding to 0, 70, 85, and 100 mm Hg for 3 h. Relative gene expression of lacZ, directly reflecting MMP promoter activity, was then quantified by QPCR.

Results: MMP-2 promoter activity decreased to 0.42 +/- 0.11 at 0 mm Hg and increased to 1.57 +/- 0.24-fold at 100 mm Hg (P < 0.05), whereas MMP-9 was unaffected.

Conclusions: Using unique transgenic constructs with homology to human MMP promoters, this study demonstrated that a physiologically relevant mechanical stimulus was sufficient to differentially induce MMP promoter activation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Aorta, Thoracic / physiology*
  • Female
  • Gene Expression Regulation, Enzymologic / physiology*
  • Genes, Reporter / physiology
  • Lac Operon
  • Male
  • Matrix Metalloproteinase 2 / genetics*
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / genetics*
  • Matrix Metalloproteinase 9 / metabolism
  • Mice
  • Mice, Transgenic
  • Promoter Regions, Genetic / physiology
  • RNA, Messenger / metabolism
  • Rabbits
  • Rats
  • Stress, Mechanical
  • Vasoconstriction / physiology*

Substances

  • RNA, Messenger
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9