A caveolin dominant negative mutant associates with lipid bodies and induces intracellular cholesterol imbalance

J Cell Biol. 2001 Mar 5;152(5):1057-70. doi: 10.1083/jcb.152.5.1057.

Abstract

Recent studies have indicated a role for caveolin in regulating cholesterol-dependent signaling events. In the present study we have analyzed the role of caveolins in intracellular cholesterol cycling using a dominant negative caveolin mutant. The mutant caveolin protein, cav-3(DGV), specifically associates with the membrane surrounding large lipid droplets. These structures contain neutral lipids, and are accessed by caveolin 1-3 upon overexpression. Fluorescence, electron, and video microscopy observations are consistent with formation of the membrane-enclosed lipid rich structures by maturation of subdomains of the ER. The caveolin mutant causes the intracellular accumulation of free cholesterol (FC) in late endosomes, a decrease in surface cholesterol and a decrease in cholesterol efflux and synthesis. The amphiphile U18666A acts synergistically with cav(DGV) to increase intracellular accumulation of FC. Incubation of cells with oleic acid induces a significant accumulation of full-length caveolins in the enlarged lipid droplets. We conclude that caveolin can associate with the membrane surrounding lipid droplets and is a key component involved in intracellular cholesterol balance and lipid transport in fibroblasts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Androstenes / pharmacology
  • Animals
  • Antibodies
  • Biological Transport / drug effects
  • Biomarkers / analysis
  • Brefeldin A / pharmacology
  • Caveolin 1
  • Caveolins / chemistry
  • Caveolins / genetics
  • Caveolins / metabolism*
  • Cell Line
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Cholesterol / metabolism*
  • Cricetinae
  • Cytoplasmic Vesicles / chemistry
  • Cytoplasmic Vesicles / drug effects
  • Cytoplasmic Vesicles / metabolism*
  • Cytoplasmic Vesicles / ultrastructure
  • Endoplasmic Reticulum / chemistry
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / metabolism
  • Endosomes / chemistry
  • Endosomes / metabolism
  • Fibroblasts
  • Fluorescent Antibody Technique
  • Genes, Dominant / genetics
  • Homeostasis
  • Lipid Metabolism*
  • Microscopy, Electron
  • Microscopy, Video
  • Mutation / genetics*
  • Oleic Acid / pharmacology
  • Signal Transduction

Substances

  • Androstenes
  • Antibodies
  • Biomarkers
  • Caveolin 1
  • Caveolins
  • Brefeldin A
  • Oleic Acid
  • 3-beta-(2-(diethylamino)ethoxy)androst-5-en-17-one
  • Cholesterol