Identification of a gamma-interferon-responsive element in the promoter of the human macrophage scavenger receptor A gene

Arterioscler Thromb Vasc Biol. 2001 May;21(5):825-31. doi: 10.1161/01.atv.21.5.825.

Abstract

In the present study, we demonstrate gamma-interferon (gamma-IFN)-inducible scavenger receptor A (SR-A) mRNA expression during the early stages of THP-1 and blood monocyte differentiation. Predominant induction of SR-A type II mRNA parallels the increased accumulation of cholesteryl esters under these conditions. A potential signal transducer and activator of transcription (STAT1) binding site (gamma-interferon activation site) in the SR-A promoter demonstrates gamma-IFN-inducible DNA binding activity and is most likely responsible for the gamma-IFN-dependent expression of an SR-A promoter-luciferase fusion construct. In contrast, gamma-IFN inhibits SR-A expression in mature macrophages as well as after prolonged gamma-IFN incubation of THP-1 monocytes. Taken together, these results demonstrate opposite effects of gamma-IFN on SR-A expression and activity during the early versus late stages of monocyte maturation. gamma-IFN-induced STAT1 activation, leading to increased SR-A expression, could therefore play an important role in the initial steps of foam cell formation and xanthomatosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell Differentiation
  • Cell Line
  • DNA-Binding Proteins / metabolism
  • Female
  • Genes
  • Humans
  • Interferon-gamma / pharmacology*
  • Macrophages / metabolism
  • Male
  • Middle Aged
  • Monocytes / drug effects
  • Monocytes / metabolism*
  • Promoter Regions, Genetic*
  • Protein Isoforms / biosynthesis
  • Protein Isoforms / genetics
  • RNA, Messenger / biosynthesis
  • Receptors, Immunologic / biosynthesis
  • Receptors, Immunologic / genetics*
  • Receptors, Immunologic / metabolism
  • Receptors, Scavenger
  • Response Elements
  • STAT1 Transcription Factor
  • Scavenger Receptors, Class A
  • Trans-Activators / metabolism

Substances

  • DNA-Binding Proteins
  • Protein Isoforms
  • RNA, Messenger
  • Receptors, Immunologic
  • Receptors, Scavenger
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Scavenger Receptors, Class A
  • Trans-Activators
  • Interferon-gamma