Fas/FADD-mediated activation of a specific program of inflammatory gene expression in vascular smooth muscle cells

Nat Med. 2000 Jul;6(7):790-6. doi: 10.1038/77521.

Abstract

Apoptosis of smooth muscle cells is a common feature of vascular lesions but its pathophysiological significance is not known. We demonstrate that signals initiated by regulated Fas-associated death domain protein overexpression in rat vascular smooth muscle cells in the carotid artery induce expression of monocyte-chemoattractant protein-1 and interleukin-8, and cause massive immigration of macrophages in vivo. These chemokines, and a specific set of other pro-inflammatory genes, are also upregulated in human vascular smooth muscle cells during Fas-induced apoptosis, in part through a process that requires interleukin-1alpha activation. Induction of a pro-inflammatory program by apoptotic vascular smooth muscle cells may thus contribute to the pathogenesis of vascular disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Animals
  • Apoptosis*
  • Carotid Arteries / immunology
  • Carotid Arteries / pathology
  • Carrier Proteins / metabolism*
  • Caspases / metabolism
  • Chemokine CCL2 / biosynthesis
  • Fas-Associated Death Domain Protein
  • Gene Expression Regulation
  • Humans
  • Inflammation / genetics*
  • Interleukin-1 / metabolism
  • Interleukin-8 / biosynthesis
  • Muscle, Smooth, Vascular / immunology*
  • Rats
  • Rats, Inbred F344
  • Up-Regulation
  • fas Receptor / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • Chemokine CCL2
  • FADD protein, human
  • Fadd protein, rat
  • Fas-Associated Death Domain Protein
  • Interleukin-1
  • Interleukin-8
  • fas Receptor
  • Caspases