Chylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defects

Circ Cardiovasc Genet. 2010 Apr;3(2):169-78. doi: 10.1161/CIRCGENETICS.109.908905. Epub 2010 Feb 2.

Abstract

Background: Recent studies in mice have established that an endothelial cell protein, glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPIHBP1), is essential for the lipolytic processing of triglyceride-rich lipoproteins.

Methods and results: We report the discovery of a homozygous missense mutation in GPIHBP1 in a young boy with severe chylomicronemia. The mutation, p.C65Y, replaces a conserved cysteine in the GPIHBP1 lymphocyte antigen 6 domain with a tyrosine and is predicted to perturb protein structure by interfering with the formation of a disulfide bond. Studies with transfected Chinese hamster ovary cells showed that GPIHBP1-C65Y reaches the cell surface but has lost the ability to bind lipoprotein lipase (LPL). When the GPIHBP1-C65Y homozygote was given an intravenous bolus of heparin, only trace amounts of LPL entered the plasma. We also observed very low levels of LPL in the postheparin plasma of a subject with chylomicronemia who was homozygous for a different GPIHBP1 mutation (p.Q115P). When the GPIHBP1-Q115P homozygote was given a 6-hour infusion of heparin, a significant amount of LPL appeared in the plasma, resulting in a fall in the plasma triglyceride levels from 1780 to 120 mg/dL.

Conclusions: We identified a novel GPIHBP1 missense mutation (p.C65Y) associated with defective LPL binding in a young boy with severe chylomicronemia. We also show that homozygosity for the C65Y or Q115P mutations is associated with low levels of LPL in the postheparin plasma, demonstrating that GPIHBP1 is important for plasma triglyceride metabolism in humans.

Publication types

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

MeSH terms

  • Amino Acid Substitution
  • Animals
  • CHO Cells
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics*
  • Child, Preschool
  • Chylomicrons / blood*
  • Cricetinae
  • Cricetulus
  • Exons
  • Heparin / pharmacology
  • Homozygote
  • Humans
  • Lipoprotein Lipase / blood*
  • Lipoprotein Lipase / metabolism
  • Male
  • Mutation, Missense
  • Receptors, Lipoprotein
  • Triglycerides / blood

Substances

  • Carrier Proteins
  • Chylomicrons
  • GPIHBP1 protein, human
  • Receptors, Lipoprotein
  • Triglycerides
  • Heparin
  • Lipoprotein Lipase