Electronegative low-density lipoprotein. A link between apolipoprotein B misfolding, lipoprotein aggregation and proteoglycan binding

Curr Opin Lipidol. 2012 Oct;23(5):479-86. doi: 10.1097/MOL.0b013e328357c933.

Abstract

Purpose of review: Subendothelial retention of lipoproteins is considered the first step in the development of atherosclerosis, but the molecular mechanisms involved are poorly understood. Recent findings on the atherogenic properties of a minor electronegative fraction of LDL (LDL(-)) could contribute to a better understanding of this process.

Recent findings: Circular dichroism, Trp-fluorescence and two-dimensional nuclear magnetic resonance have shown that apolipoprotein B (apoB) in LDL(-) has an abnormal, misfolded conformation. Immunochemical analysis revealed a different conformation, mainly in the N-terminal and C-terminal extremes. These alterations contribute to the high susceptibility to aggregation of LDL(-). Moreover, LDL(-) can seed the aggregation of native LDL, suggesting an amyloidogenic character that has been attributed to the amphipathic helix cluster in the α2-domain. A phospholipase C (PLC)-like activity associated to LDL(-) seems to play a major role in the LDL(-)-induced aggregation. The aggregation of LDL(-) increases its binding to proteoglycans because of the abnormal conformation of the N-terminal extreme of apoB.

Summary: LDL(-) could play a relevant role in atherogenesis by acting as a priming factor that stimulates lipoprotein aggregation. This process, which appears to be mediated by a PLC-like activity intrinsic to LDL(-), increases the binding of LDL to proteoglycans and could promote subendothelial retention of these lipoproteins.

Publication types

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

MeSH terms

  • Apolipoproteins B / chemistry*
  • Atherosclerosis / blood
  • Atherosclerosis / pathology*
  • Circular Dichroism
  • Endothelial Cells / chemistry
  • Enzyme Activation
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Lipoproteins / chemistry*
  • Lipoproteins, LDL / chemistry*
  • Magnetic Resonance Spectroscopy
  • Protein Binding
  • Protein Conformation
  • Protein Folding
  • Proteoglycans / chemistry*
  • Type C Phospholipases / metabolism

Substances

  • Apolipoproteins B
  • Lipoproteins
  • Lipoproteins, LDL
  • Proteoglycans
  • oxidized low density lipoprotein
  • Type C Phospholipases