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Journal of Lipid Research, Vol 38, 1445-1453, Copyright © 1997 by Lipid Research, Inc.
S Dueland, D France, SL Wang, JD Trawick and RA Davis
C57BL/6 mice are susceptible to diet-induced atherosclerosis, whereas
BALB/c mice are resistant. The susceptibility of C57BL/6 mice has been
linked to decreased plasma HDL cholesterol in response to a diet containing
fat, cholesterol, and cholic acid. Feeding C57BL/6 mice a diet consisting
of fat and cholesterol, but no cholic acid, increased plasma high density
lipoprotein (HDL) cholesterol. The increase in HDL was associated with
increases in both plasma apolipoprotein (apo)A-I and hepatic apoA-I mRNA.
Supplementation of the cholesterol-rich diet with cholic acid inhibited the
stimulatory effect of cholesterol on hepatic apoA-I mRNA expression,
resulting in similar hepatic apoA-I mRNA levels compared to chow-fed mice.
Atherosclerosis-resistant BALB/c mice were also resistant to diet-induced
changes in plasma HDL, apoA-I, and hepatic apoA-I mRNA levels. Previous
studies showed that the diets changed both the activity and mRNA encoding
the liver specific enzyme 7alpha-hydroxylase (1993.J. Lipid Res. 34:
923-931). In both strains of mice, hepatic expression of apoA-I and
7alpha-hydroxylase mRNA varied in parallel. Whereas susceptible C57BL/6
mice also showed a significant correlation between HDL cholesterol and
expression of 7alpha- hydroxylase, no such correlation was observed in
BALB/c mice, suggesting that genetic differences in HDL metabolism, not
hepatic apoA- I synthesis, are responsible for the strain specific
differences in plasma HDL levels. The finding that lecithin: cholesterol
acyltransferase (LCAT) activity was significantly decreased in C57BL/6
mice, but not in BALB/ c mice fed the atherogenic diet, further supports
this conclusion. Additional studies show that McArdle hepatoma cells stably
expressing plasmid-derived rat 7alpha-hydroxylase recapitulated the
parallel linear relationship between 7alpha- hydroxylase and apoA-I mRNA
expression observed in both strains of mice. These data link hepatic apoA-I
mRNA expression to hepatic cholesterol/bile acid metabolism.
ARTICLES
Cholesterol 7alpha-hydroxylase influences the expression of hepatic apoA-I in two inbred mouse strains displaying different susceptibilities to atherosclerosis and in hepatoma cells
Department of Biology, San Diego State University, CA 92182-0057, USA.
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