Corticosteroids are synthesized from cholesterol which may arise from de no
vo synthesis or from the uptake of low or high density lipoproteins (LDL or
HDL). In the present study, we compared the expression and regulation patt
erns of LDL receptor and CLA-1 (CD36 and LIMPII Analogous-1, an HDL recepto
r) genes in adult human adrenocortical tissues to shed more light on the re
lative contribution of LDL and HDL in human adrenal steroidogenesis. By scr
eening 64 normal and pathological adrenal samples by Northern blotting, we
found a positive correlation between LDL receptor and CLA-1 mRNA expression
in the adrenal tissues (r=0.547; spearman rank correlation test P<0.01). A
drenal tissues adjacent to Gushing's adenomas contained consistently less L
DL receptor and CLA-1 mRNA than normal adrenals (Mann-Whitney P < 0.05). In
primary cultures of normal adrenal cells, accumulation of both LDL recepto
r and CLA-1 mRNAs was upregulated by ACTH in a dose- and time-dependent man
ner, with an earlier induction of LDL receptor than CLA-1 mRNA expression.
(Bu)(2)cAMP also increased the levels of these two mRNAs. Addition of LDL,
but not HDL, into the culture medium increased cortisol production in untre
ated adrenocortical cells. Both LDL and HDL enhanced ACTH-induced cortisol
production, with the effect of LDL much stronger than that of HDL. Our data
show that LDL receptor and CLA-1's expression is ACTH-dependent and occurs
in parallel in human adrenal tissues. LDL rather than HDL may be used as t
he preferential source of cholesterol for steroidogenesis in human adult ad
renocortical cells.