Activation of transcription factors and gene expression by oxidized low-density lipoprotein

Free Radic Biol Med. 2009 Jan 15;46(2):127-37. doi: 10.1016/j.freeradbiomed.2008.10.024. Epub 2008 Nov 1.

Abstract

It is well recognized that oxidized LDL (OxLDL) plays a crucial role in the initiation and progression of atherosclerosis. Many biological effects of OxLDL are mediated through signaling pathways, especially via the activation of transcription factors, which in turn stimulate the expression of genes involved in the inflammatory and oxidative stress response or in cell cycle regulation. In this review, we will discuss the various transcription factors activated by OxLDL, the studied cell types, the active compounds of the OxLDL particle, and the downstream genes when identified. Identification of the transcription factors and some of the downstream genes regulated by OxLDL has helped us understand the molecular mechanism involved in generation of the atherosclerotic plaque.

Publication types

  • Review

MeSH terms

  • Animals
  • Atherosclerosis / genetics
  • Atherosclerosis / immunology*
  • Cell Cycle
  • Feedback, Physiological
  • Humans
  • Hypoxia-Inducible Factor 1 / genetics
  • Hypoxia-Inducible Factor 1 / immunology
  • Hypoxia-Inducible Factor 1 / metabolism
  • Inflammation
  • Lipoproteins, LDL / genetics*
  • Lipoproteins, LDL / immunology
  • Lipoproteins, LDL / metabolism
  • NF-E2-Related Factor 2 / genetics
  • NF-E2-Related Factor 2 / immunology
  • NF-E2-Related Factor 2 / metabolism
  • NF-kappa B / genetics
  • NF-kappa B / immunology
  • NF-kappa B / metabolism
  • NFATC Transcription Factors / genetics
  • NFATC Transcription Factors / immunology
  • NFATC Transcription Factors / metabolism
  • Oxidative Stress
  • Peroxisome Proliferator-Activated Receptors / genetics
  • Peroxisome Proliferator-Activated Receptors / immunology
  • Peroxisome Proliferator-Activated Receptors / metabolism
  • STAT Transcription Factors / immunology
  • Signal Transduction
  • Smad3 Protein / genetics
  • Smad3 Protein / immunology
  • Smad3 Protein / metabolism
  • Transcription Factor AP-1 / genetics
  • Transcription Factor AP-1 / immunology
  • Transcription Factor AP-1 / metabolism
  • Transcriptional Activation / immunology*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / immunology
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Hypoxia-Inducible Factor 1
  • Lipoproteins, LDL
  • NF-E2-Related Factor 2
  • NF-kappa B
  • NFATC Transcription Factors
  • Peroxisome Proliferator-Activated Receptors
  • STAT Transcription Factors
  • Smad3 Protein
  • Transcription Factor AP-1
  • Tumor Suppressor Protein p53
  • oxidized low density lipoprotein