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


Autoria(s): Pol, Albert; Luetterforst, Robert; Lindsay, Margaret; Heino, Sanna; Ikonen, Elina; Parton, Robert G.
Data(s)

05/03/2001

Resumo

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.

Identificador

http://espace.library.uq.edu.au/view/UQ:60925/UQ60925_OA.pdf

http://espace.library.uq.edu.au/view/UQ:60925

Idioma(s)

eng

Publicador

The Rockefeller University Press

Palavras-Chave #Cell Biology #Caveolin #Caveolae #Cholesterol #Lipid Droplets #Endoplasmic Reticulum #Trans-golgi-network #Plasma-membrane #Endoplasmic-reticulum #Chaperone Complex #Binding Protein #Mdck Cells #Localization #Pathway #Identification #Compartment
Tipo

Journal Article