Corticosteroid effect on Caco-2 cell lipids depends on cell differentiation

Š Jindřichová, O Novakova, J Bryndova… - The Journal of Steroid …, 2003 - Elsevier
Š Jindřichová, O Novakova, J Bryndova, E Tvrzicka, V Lisa, F Novak, J Pacha
The Journal of Steroid Biochemistry and Molecular Biology, 2003Elsevier
Previous studies from our laboratory have indicated that secondary hyperaldosteronism
affects phospholipids of rat colonic enterocytes. To assess whether this represents a direct
effect of mineralocorticoids on enterocytes, the role of aldosterone and dexamethasone in
the regulation of lipid metabolism was examined in Caco-2 cells during development of their
enterocyte phenotype. Differentiation of Caco-2 cells was associated with increased levels
of triglycerides (TG) and cholesteryl esters (CE), a decreased content of cholesterol and …
Previous studies from our laboratory have indicated that secondary hyperaldosteronism affects phospholipids of rat colonic enterocytes. To assess whether this represents a direct effect of mineralocorticoids on enterocytes, the role of aldosterone and dexamethasone in the regulation of lipid metabolism was examined in Caco-2 cells during development of their enterocyte phenotype. Differentiation of Caco-2 cells was associated with increased levels of triglycerides (TG) and cholesteryl esters (CE), a decreased content of cholesterol and phospholipids and changes in individual phospholipid classes. The phospholipids of differentiated cells had a higher content of n-6 polyunsaturated fatty acids (PUFA) and lower amounts of monounsaturated (MUFA) and saturated fatty acids than subconfluent undifferentiated cells. Differentiated cells exhibited a higher ability to incorporate [3H ]arachidonic acid (AA) into cellular phospholipids and a lower ability for incorporation into TG and CE. Incubation of subconfluent undifferentiated cells with aldosterone or dexamethasone was without effect on the content of lipids, their fatty acids and [3H ]AA incorporation. In contrast, aldosterone treatment of differentiated cells diminished the content of TG, increased the content of phospholipids and modulated their fatty acid composition. The percentage of n-6 and n-3 PUFA in phospholipids was increased and that of MUFA decreased, whereas no changes in TG were observed. The incorporation of [3H ]AA into phospholipids was increased and into TG decreased and these changes were blocked by spironolactone. Treatment of differentiated cells with dexamethasone increased their CE content but no effect was identified upon other lipids, their fatty acid composition and on the incorporation of [3H ]AA. As expected for the involvement of corticosteroid hormones the mineralocorticoid and glucocorticoid receptors were identified in Caco-2 cells by RT-PCR. The results suggest that aldosterone had a profound influence on lipid metabolism in enterocytes and that its effect depends on the stage of differentiation. The aldosterone-dependent changes occurring in phospholipids and their fatty acid composition may reflect a physiologically important phenomenon with long-term consequences for membrane structure and function.
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