Key result
Caveolin-1-null fat cells exhibited a modestly enhanced rate of lipolysis and reduced cellular integrity compared with reconstituted cells, suggesting caveolae protect adipocytes from lipotoxicity.
Caveolae appear to protect adipocytes from the lipotoxic effects of elevated fatty acids by forming detergent-resistant membrane domains.
No immediate clinical implications; leaves open caveolae protection against human adipocyte lipotoxicity.
Mice and humans lacking functional caveolae are dyslipidemic and have reduced fat stores and smaller fat cells. To test the role of caveolins/caveolae in maintaining lipid stores and adipocyte integrity, we compared lipolysis in caveolin-1 (Cav1)-null fat cells to that in cells reconstituted for caveolae by caveolin-1 re-expression. We find that the Cav1-null cells have a modestly enhanced rate of lipolysis and reduced cellular integrity compared with reconstituted cells as determined by the release of lipid metabolites and lactic dehydrogenase, respectively, into the media. There are no apparent differences in the levels of lipolytic enzymes or hormonally stimulated phosphorylation events in the two cell lines. In addition, acute fasting, which dramatically raises circulating fatty acid levels in vivo, causes a significant upregulation of caveolar protein constituents. These results are consistent with the hypothesis that caveolae protect fat cells from the lipotoxic effects of elevated levels fatty acids, which are weak detergents at physiological pH, by virtue of the property of caveolae to form detergent-resistant membrane domains.
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Meshulam et al. (2011) studied Lipotoxicity. Caveolin-1 (Cav1)-null fat cells vs. Cells reconstituted for caveolae by caveolin-1 re-expression was evaluated on Rate of lipolysis and cellular integrity (release of lipid metabolites and lactic dehydrogenase). Caveolin-1-null fat cells exhibited a modestly enhanced rate of lipolysis and reduced cellular integrity compared with reconstituted cells, suggesting caveolae protect adipocytes from lipotoxicity.
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