Cholesterol regulates high-density lipoprotein interaction with isolated epithelial cells of human small intestine

Abstract

The effect of cholesterol on the interaction of high-density lipoprotein (HDL) with isolated human small intestine epithelial cells (enterocytes) was studied. 125I-labeled HDL 3 binding by these cells was enhanced in response to cholesterol loading of the cells in a time- and dose- dependent manner. Preincubation of the cells with cholesterol led to the enhancement both of the number of binding sites and the binding affinity. The enhancement of binding correlated with the cellular cholesterol content. Cycloheximide (0.5 mM) inhibited uptake of cholesterol by enterocytes and blocked its effect on 125I-labeled HDL 3 binding. The effect of cholesterol on 125I-labeled HDL 3 degradation had a double-phase character. At concentrations 10–20 μg/ml, the degradation rate was rapidly elevated, but further increase in cholesterol concentration led to a fall in the degradation rate. Incubation of enterocytes with HDL 3 resulted in the efflux of cholesterol from cells and its incorporation into HDL 3. The results obtained make it possible to assume that binding and degradation of 125I-labeled HDL 3 by human enterocytes are independently regulated by the cell total cholesterol content. Binding of HDL by enterocytes may result both in the degradation of HDL and cholesterol efflux from cells.