Inflammation modulates human HDL composition and function in vivo

Atherosclerosis. 2012 Jun;222(2):390-4. doi: 10.1016/j.atherosclerosis.2012.02.032. Epub 2012 Feb 28.

Abstract

Objectives: Inflammation may directly impair HDL functions, in particular reverse cholesterol transport (RCT), but limited data support this concept in humans.

Methods and results: We employed low-dose human endotoxemia to assess the effects of inflammation on HDL and RCT-related parameters in vivo. Endotoxemia induced remodelling of HDL with depletion of pre-β1a HDL particles determined by 2-D gel electrophoresis (-32.2±9.3% at 24 h, p<0.05) as well as small (-23.0±5.1%, p<0.01, at 24 h) and medium (-57.6±8.0% at 16 h, p<0.001) HDL estimated by nuclear magnetic resonance (NMR). This was associated with induction of class II secretory phospholipase A2 (~36 fold increase) and suppression of lecithin:cholesterol acyltransferase activity (-20.8±3.4% at 24 h, p<0.01) and cholesterol ester transfer protein mass (-22.2±6.8% at 24 h, p<0.001). The HDL fraction, isolated following endotoxemia, had reduced capacity to efflux cholesterol in vitro from SR-BI and ABCA1, but not ABCG1 transporter cell models.

Conclusions: These data support the concept that "atherogenic-HDL dysfunction" and impaired RCT occur in human inflammatory syndromes, largely independent of changes in plasma HDL-C and ApoA-I levels.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter 1
  • ATP Binding Cassette Transporter, Subfamily G, Member 1
  • ATP-Binding Cassette Transporters / metabolism
  • Adult
  • Animals
  • Apolipoprotein A-I / blood
  • Cell Line
  • Cholesterol Ester Transfer Proteins / metabolism
  • Cholesterol, HDL / blood*
  • Electrophoresis, Gel, Two-Dimensional
  • Endotoxemia / blood
  • Endotoxemia / complications
  • Female
  • Group II Phospholipases A2 / metabolism
  • High-Density Lipoproteins, Pre-beta / blood*
  • Humans
  • Inflammation / blood*
  • Inflammation / etiology
  • Magnetic Resonance Spectroscopy
  • Male
  • Mice
  • Particle Size
  • Phosphatidylcholine-Sterol O-Acyltransferase / metabolism
  • Rats
  • Scavenger Receptors, Class B / metabolism
  • Time Factors
  • Young Adult

Substances

  • ABCA1 protein, human
  • ABCG1 protein, human
  • APOA1 protein, human
  • ATP Binding Cassette Transporter 1
  • ATP Binding Cassette Transporter, Subfamily G, Member 1
  • ATP-Binding Cassette Transporters
  • Apolipoprotein A-I
  • CETP protein, human
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • High-Density Lipoproteins, Pre-beta
  • Scavenger Receptors, Class B
  • Phosphatidylcholine-Sterol O-Acyltransferase
  • Group II Phospholipases A2