Sh. Quarfordt et al., THE INFLUENCE OF CHOLESTERYL ESTER CONTENT ON HEPATOCYTE TRIOLEIN EMULSION UPTAKE, Biochimica et biophysica acta, L. Lipids and lipid metabolism, 1255(1), 1995, pp. 82-86
When triolein emulsions are enriched with cholesteryl oleate they are
more readily removed by primary rat hepatocytes and HepG2 cells via an
apolipoprotein E-responsive pathway. The increment in the cholesteryl
ester does not appreciably change the size of the emulsion or its aff
inity for the apo E protein. The cholesteryl ester enriched-emulsion d
emonstrates increased apo E-mediated HepG2-binding as well as endocyto
sis. The higher the content of cholesteryl ester of the particle, the
greater was both the binding and the endocytosis. The increased endocy
tosis was associated with increased degradation of the apo E. Choleste
ryl linoleate and palmitate produced the same effects as the oleate. L
ecithin-cholesterol acyltransferase additions were also able to increa
se the HepG2 uptake of the emulsion. The data indicates that the incre
ment in cholesterol ester occurring during maturation of plasma triacy
lglycerol-rich particles facilitates hepatic remnant assimilation by a
n apo E-dependent pathway.