Flotillin-1 stabilizes caveolin-1 in intestinal epithelial cells
Flotillin-1 stabilizes caveolin-1 in intestinal epithelial cells
Flotillins and caveolins represent two types of resident proteins associated with lipid rafts in mammalian cells, however, their possible cross-talk in regulating lipid raft functions remains poorly understood. In this report, we observed that siRNA-mediated down-regulation of flotillin-1 expression which disrupted lipid raft-mediated endocytosis of BODIPY FL C(5)-lactosylceramide also substantially decreased caveolin-1 level in SK-CO15 human intestinal epithelial cells. The decrease in caveolin-1 expression appeared to be specific for flotillin-1 knock-down and was not observed after down-regulation of flotillin-2. The decrease in caveolin-1 level in flotillin-1-depleted cells was not due to suppression of its mRNA synthesis and was not mimicked by cholesterol depletion of SK-CO15 cells. Furthermore, flotillin-1 dependent down-regulation of caveolin-1 was reversed after cell exposure to lysosomal inhibitor, chloroquine but not proteosomal inhibitor, MG262. Our data suggest that flotillin-1 regulates caveolin-1 level by preventing its lysosomal degradation in intestinal epithelial cells.
- Emory University United States
- University of Rochester United States
Boron Compounds, Caveolin 1, Lactosylceramides, Humans, Membrane Proteins, Intestinal Mucosa, Lysosomes, Endocytosis, Cell Line
Boron Compounds, Caveolin 1, Lactosylceramides, Humans, Membrane Proteins, Intestinal Mucosa, Lysosomes, Endocytosis, Cell Line
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