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1Veterans Affairs Palo Alto Health Care System, Palo Alto; 2Department of Medicine, Stanford University, Stanford, California; 3Department of Metabolic Disease, University of Tokyo, Tokyo; and 4Department of Internal Medicine, Jichi Medical School, Tochigi, Japan
Submitted 18 August 2006 ; accepted in final form 16 September 2006
Steroid hormones are synthesized using cholesterol as precursor. To determine the functional importance of the low density lipoprotein (LDL) receptor and hormone-sensitive lipase (HSL) in adrenal steroidogenesis, adrenal cells were isolated from control, HSL/, LDLR/, and double LDLR/HSL/ mice. The endocytic and selective uptake of apolipoprotein E-free human high density lipoprotein (HDL)-derived cholesteryl esters did not differ among the mice, with selective uptake accounting for >97% of uptake. In contrast, endocytic uptake of either human LDL- or rat HDL-derived cholesteryl esters was reduced 8085% in LDLR/ and double-LDLR/HSL/ mice. There were no differences in the selective uptake of either human LDL- or rat HDL-derived cholesteryl esters among the mice. Maximum corticosterone production induced by ACTH or dibutyryl cyclic AMP and lipoproteins was not altered in LDLR/ mice but was reduced 8090% in HSL/ mice. Maximum corticosterone production was identical in HSL/ and double-LDLR/HSL/ mice. These findings suggest that, although the LDL receptor is responsible for endocytic delivery of cholesteryl esters from LDL and rat HDL to mouse adrenal cells, it appears to play a negligible role in the delivery of cholesterol for acute adrenal steroidogenesis in the mouse. In contrast, HSL occupies a vital role in adrenal steroidogenesis because of its link to utilization of selectively delivered cholesteryl esters from lipoproteins.
neutral cholesteryl ester hydrolase; corticosterone; cholesterol; receptor low density lipoprotein; selective pathway; hormone-sensitive lipase
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