Atherogenic diet leads to posttranslational down-regulation of murine hepatocyte SR-BI expression.
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Atherogenic diet leads to posttranslational down-regulation of murine hepatocyte SR-BI expression. / Niemeier, Andreas; Kovacs, Werner J; Strobl, Wolfgang; Stangl, Herbert.
In: ATHEROSCLEROSIS, Vol. 202, No. 1, 1, 2009, p. 169-175.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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T1 - Atherogenic diet leads to posttranslational down-regulation of murine hepatocyte SR-BI expression.
AU - Niemeier, Andreas
AU - Kovacs, Werner J
AU - Strobl, Wolfgang
AU - Stangl, Herbert
PY - 2009
Y1 - 2009
N2 - The scavenger receptor class B, type I (SR-BI) mediates selective cholesteryl ester uptake by the liver and thereby exerts a systemic anti-atherogenic effect. It is unknown, however, whether exogenous cholesterol contributes to the regulation of hepatic SR-BI expression. Atherosclerosis resistant SJL and susceptible C57Bl/6 mice were challenged with atherogenic diets that lead to an increase of both plasma and liver cholesterol. The increase of cholesterol was accompanied by a marked posttranslational down-regulation of liver SR-BI expression. On average, we observed a threefold decrease of SR-BI protein while mRNA levels were slightly increased in both strains. Mice with transgenic over-expression of the sterol regulatory element binding proteins (SREBPs) were used as a model that displays endogenously increased liver cholesterol concentrations. In SREBP-1a and -1c transgenic mice on normal chow, SR-BI was transcriptionally down-regulated. When fed the atherogenic diet, the posttranslational SR-BI regulation was still functional on this background. Down-regulation of SR-BI did not alter the hepatocyte surface expression pattern, but was accompanied by a decrease of PDZK1, an adaptor protein recently identified to control SR-BI protein expression levels in the liver and intestine. Taken together, a diet-induced increase of plasma and hepatic cholesterol levels leads to a posttranscriptional down-regulation of SR-BI in mouse liver via a mechanism likely involving PDZK1.
AB - The scavenger receptor class B, type I (SR-BI) mediates selective cholesteryl ester uptake by the liver and thereby exerts a systemic anti-atherogenic effect. It is unknown, however, whether exogenous cholesterol contributes to the regulation of hepatic SR-BI expression. Atherosclerosis resistant SJL and susceptible C57Bl/6 mice were challenged with atherogenic diets that lead to an increase of both plasma and liver cholesterol. The increase of cholesterol was accompanied by a marked posttranslational down-regulation of liver SR-BI expression. On average, we observed a threefold decrease of SR-BI protein while mRNA levels were slightly increased in both strains. Mice with transgenic over-expression of the sterol regulatory element binding proteins (SREBPs) were used as a model that displays endogenously increased liver cholesterol concentrations. In SREBP-1a and -1c transgenic mice on normal chow, SR-BI was transcriptionally down-regulated. When fed the atherogenic diet, the posttranslational SR-BI regulation was still functional on this background. Down-regulation of SR-BI did not alter the hepatocyte surface expression pattern, but was accompanied by a decrease of PDZK1, an adaptor protein recently identified to control SR-BI protein expression levels in the liver and intestine. Taken together, a diet-induced increase of plasma and hepatic cholesterol levels leads to a posttranscriptional down-regulation of SR-BI in mouse liver via a mechanism likely involving PDZK1.
M3 - SCORING: Zeitschriftenaufsatz
VL - 202
SP - 169
EP - 175
JO - ATHEROSCLEROSIS
JF - ATHEROSCLEROSIS
SN - 0021-9150
IS - 1
M1 - 1
ER -