Identification of a danger-associated peptide from apolipoprotein B100 (ApoBDS-1) that triggers innate proatherogenic responses

Circulation. 2011 Nov 29;124(22):2433-43, 1-7. doi: 10.1161/CIRCULATIONAHA.111.051599. Epub 2011 Nov 7.

Abstract

Background: Subendothelial deposited low-density lipoprotein particles are a known inflammatory factor in atherosclerosis. However, the causal components derived from low-density lipoprotein are still poorly defined. Apolipoprotein B100 (ApoB100) is the unexchangeable protein component of low-density lipoprotein, and the progression of atherosclerosis is associated with immune responses to ApoB100-derived peptides. In this study, we analyzed the proinflammatory activity of ApoB100 peptides in atherosclerosis.

Methods and results: By screening a peptide library of ApoB100, we identified a distinct native peptide referred to as ApoB100 danger-associated signal 1 (ApoBDS-1), which shows sequence-specific bioactivity in stimulation of interleukin-8, CCL2, and interleukin-6. ApoBDS-1 activates mitogen-activated protein kinase and calcium signaling, thereby effecting the expression of interleukin-8 in innate immune cells. Ex vivo stimulation of carotid plaques with ApoBDS-1 enhances interleukin-8 and prostaglandin E₂ release. Furthermore, we demonstrated that ApoBDS-1-positive peptide fragments are present in atherosclerotic lesions using immunoassays and that low-molecular-weight fractions isolated from plaque show ApoBDS-1 activity inducing interleukin-8 production.

Conclusions: Our data show that ApoBDS-1 is a previously unrecognized peptide with robust proinflammatory activity, contributing to the disease-promoting effects of low-density lipoprotein in the pathogenesis of atherosclerosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoprotein B-100 / physiology*
  • Atherosclerosis / pathology
  • Atherosclerosis / physiopathology*
  • Calcium / physiology
  • Carotid Artery Diseases / pathology
  • Carotid Artery Diseases / physiopathology
  • Chemokine CCL2 / physiology
  • Humans
  • Immunity, Innate / physiology*
  • Interleukin-6 / physiology
  • Interleukin-8 / physiology
  • Mitogen-Activated Protein Kinase Kinases / physiology
  • Peptides / physiology*
  • Plaque, Atherosclerotic / pathology
  • Plaque, Atherosclerotic / physiopathology*
  • Signal Transduction / physiology

Substances

  • APOB protein, human
  • Apolipoprotein B-100
  • Chemokine CCL2
  • Interleukin-6
  • Interleukin-8
  • Peptides
  • Mitogen-Activated Protein Kinase Kinases
  • Calcium