Angptl3 regulates lipid metabolism in mice

Nat Genet. 2002 Feb;30(2):151-7. doi: 10.1038/ng814. Epub 2002 Jan 14.

Abstract

The KK obese mouse is moderately obese and has abnormally high levels of plasma insulin (hyperinsulinemia), glucose (hyperglycemia) and lipids (hyperlipidemia). In one strain (KK/San), we observed abnormally low plasma lipid levels (hypolipidemia). This mutant phenotype is inherited recessively as a mendelian trait. Here we report the mapping of the hypolipidemia (hypl) locus to the middle of chromosome 4 and positional cloning of the autosomal recessive mutation responsible for the hypolipidemia. The hypl locus encodes a unique angiopoietin-like lipoprotein modulator, which we named Allm1. It is identical to angiopoietin-like protein 3, encoded by Angptl3, and has a highly conserved counterpart in humans. Overexpression of Angptl3 or intravenous injection of the purified protein in KK/San mice elicited an increase in circulating plasma lipid levels. This increase was also observed in C57BL/6J normal mice. Taken together, these data suggest that Angptl3 regulates lipid metabolism in animals.

MeSH terms

  • Amino Acid Sequence
  • Angiopoietin-Like Protein 3
  • Angiopoietin-like Proteins
  • Angiopoietins
  • Animals
  • Base Sequence
  • Chromosome Mapping
  • DNA, Complementary / genetics
  • Genes, Recessive
  • Growth Substances / genetics*
  • Growth Substances / metabolism*
  • Growth Substances / pharmacology
  • Humans
  • Intercellular Signaling Peptides and Proteins*
  • Lipid Metabolism*
  • Lipids / blood
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Mice, Transgenic
  • Molecular Sequence Data
  • Mutation*
  • Phenotype

Substances

  • Angiopoietin-Like Protein 3
  • Angiopoietin-like Proteins
  • Angiopoietins
  • Angptl3 protein, mouse
  • DNA, Complementary
  • Growth Substances
  • Intercellular Signaling Peptides and Proteins
  • Lipids

Associated data

  • GENBANK/AF162224