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Journal of Lipid Research, Vol 36, 13-24, Copyright © 1995 by Lipid Research, Inc.
Palmitic acid and linoleic acid metabolism in Caco-2 cells: different triglyceride synthesis and lipoprotein secretion
MM van Greevenbroek, WF Voorhout, DW Erkelens, G van Meer and TW de Bruin
Department of Medicine, Faculty of Medicine, Utrecht University, The Netherlands.
Polarized monolayers of intestinal Caco-2 cells were used to study the
effects of saturated palmitic acid (16:0) and polyunsaturated linoleic acid
(18:2) on triglyceride synthesis and lipoprotein secretion. Monolayers were
incubated for 24 h, at the apical or lumenal side, with palmitic acid
(16:0) or linoleic acid (18:2) in physiological concentrations. Incubation
with 1.0 mM 16:0 or 18:2 resulted in differences in the composition and
amount of secreted lipoproteins. Radiolabeled lipids in the lipoproteins
secreted during incubation with 18:2 were found in the chylomicron/VLDL
(very low density lipoprotein) density whereas with 16:0 the secreted
lipoproteins were in the intermediate density/low density lipoprotein
(IDL/LDL) density range. More triglyceride was secreted into the
(basolateral) medium during incubation with 1.0 mM 18:2 (41 +/- 12% of
total triglyceride synthesized) than with 1.0 mM 16:0 (18 +/- 3% of total).
The biochemical findings correlate with conspicuous morphological changes
in the cells in the presence of 16:0, but not 18:2. Increasing
concentrations of 16:0 (0.1-1.0 mM) caused gradual accumulation of
intracellular membrane. Microvilli became strongly reduced in number. With
1.0 mM palmitic acid we found an increased incorporation of [1-
14C]palmitic acid into phosphatidic acid (14.8% of total incorporation into
phospholipid with 16:0 vs. < 0.5% with 18:2) and diacylglycerol (12.5%
with 16:0 vs. < 0.5% with 18:2) and diacylglycerol (12.5% with 16:0 vs.
0.5% with 18:2) and the amount of intracellular phospholipid doubled. The
morphological changes were completely reversed after 24 h with 1.0 mM 18:2.
We conclude from our results that, compared to 18:2, 16:0 is not
efficiently incorporated into triglycerides. 16:0 is incorporated into
cellular phospholipids in a greater proportion than 18:2, causing
accumulation of intracellular phospholipid and the precursors phosphatidic
acid and diacylglycerol. Different processing of 18:2 and 16:0 by Caco-2
cells resulted in profound differences in triglyceride synthesis and
lipoprotein composition and secretion.

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Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
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