Vol. 282, Issue 5, G817-G824, May 2002
Regulation of triacylglycerol and phospholipid trafficking by
fatty acids in newborn swine enterocytes
Ying
Yao1,
John K.
Eshun1,
Song
Lu1,
Helen M.
Berschneider2, and
Dennis D.
Black1
1 Children's Foundation Research Center at Le Bonheur
Children's Medical Center, University of Tennessee Health Science
Center, Memphis, Tennessee 38103; and 2 College of
Veterinary Medicine, North Carolina State University, Raleigh, North
Carolina 27606
We (Wang H, Berschneider HM, Du J, and
Black DD. Am J Physiol Gastrointest Liver Physiol 272:
G935-G942, 1997; Wang H, Lu S, Du J, Yao Y, Berschneider HM, and
Black DD. Am J Physiol Gastrointest Liver Physiol 280:
G1137-G1144, 2001) previously showed that different fatty acids
influence synthesis and secretion of triacylglycerol (TG) and
phospholipid (PL) in a newborn swine enterocyte cell line (IPEC-1). The
most striking effects were produced by stearic acid (SA; 18:0), which
modestly affected TG and PL synthesis but reduced TG and PL secretion,
and by eicosapentaenoic acid (EPA; 20:5), which reduced TG and PL
synthesis and TG secretion relative to oleic acid (OA; 18:1). To define
the mechanism of these effects, differentiated IPEC-1 cells were
incubated for 24 h with OA, SA, or EPA and
[3H]glycerol. Endoplasmic reticulum (ER) and Golgi (G)
content of labeled lipids and apolipoprotein (apo) B and apoAI protein
were measured. Relative to OA, SA did not impair ER TG synthesis, but reduced movement of labeled TG from ER to G. EPA impaired both ER TG
synthesis and movement of labeled TG from ER to G. PL followed the same
pattern, except ER synthesis of PL was relatively unaffected by EPA.
Carbonate treatment demonstrated decreased partitioning of labeled
lipid from ER membrane to lumen in EPA-treated cells. Organelle apoB
and apoAI content demonstrated opposite patterns after SA and EPA
incubation. We conclude that SA and EPA adversely influence immature
enterocyte ER to G lipid trafficking, compared with OA. Furthermore,
EPA inhibits ER lipid synthesis and transfer of membrane lipid to
luminal particles. Regulation of apoAI ER to G trafficking is
independent of that of apoB.
oleic acid; stearic acid; eicosapentaenoic acid; apolipoprotein