Abstract
Squalene synthetase (farnesyltransferase; farnesyl diphosphate:farnesyl-diphosphate farnesyltransferase, EC 2.5.1.21), the enzyme in the cholesterol biosynthetic pathway that converts farnesyl pyrophosphate into squalene, is subject to regulation in cultured human fibroblasts. When cholesterol-carrying low density lipoprotein (LDL) was removed from the serum of the culture medium, squalene synthetase activity increased 8-fold over 24 hr. When LDL was added back to the medium, squalene synthetase was slowly suppressed, 50% and 90% reduction occurring in 15 and 48 hr, respectively. Suppression of squalene synthetase required uptake of LDL via the LDL receptor; hence, it did not occur in mutant fibroblasts from a patient with homozygous familial hypercholesterolemia that lack receptors. The addition of a mixture of 25-hydroxycholesterol and cholesterol suppressed squalene synthetase equally well in normal and mutant fibroblasts. Coupled with previous data, the current findings indicate that cholesterol derived from LDL regulates at least two enzymes in the cholesterol synthetic pathway in fibroblasts: (i) its primary action is to rapidly suppress 3-hydroxy-3-methylglutaryl coenzyme A reductase [mevalonate:NADP(+), oxidoreductase (CoA-acylating), EC 1.1.1.34], which reduces mevalonate production by 95% within 8 hr, and (ii) its secondary action is to slowly suppress squalene synthetase. The LDL-mediated suppression of squalene synthetase does not regulate de novo cholesterol synthesis; it occurs after 3-hydroxy-3-methylglutaryl coenzyme A reductase is already suppressed. Rather, we hypothesize that it may function to allow the pool size of farnesyl pyrophosphate to be maintained in the presence of LDL so that low levels of mevalonate can be shunted preferentially into nonsterol products, such as ubiquinone-10 and dolichol. This mechanism may explain the earlier observation that the synthesis of ubiquinone-10 in fibroblasts proceeds at a normal rate in the presence of LDL despite a 95% decrease in mevalonate production.
MeSH Terms
Cells, Cultured
Cholesterol/pharmacology
Farnesyl-Diphosphate Farnesyltransferase/metabolism
Fibroblasts/enzymology
Humans
Hydroxycholesterols/pharmacology
Hydroxymethylglutaryl CoA Reductases/metabolism
Kinetics
Lipoproteins, HDL/pharmacology
Lipoproteins, LDL/metabolism,pharmacology
Oxidoreductases/metabolism
Receptors, Drug/physiology
Skin/enzymology
Chemicals
Hydroxycholesterols
Lipoproteins, HDL
Lipoproteins, LDL
Receptors, Drug
Cholesterol
Oxidoreductases
Hydroxymethylglutaryl CoA Reductases
Farnesyl-Diphosphate Farnesyltransferase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Faust J R
Goldstein J L
Brown M S
References (19)
19 references, click to expand
-
Studies on the site of the feedback control of cholesterol synthesis.
J Clin Invest. 1960 Apr;39:642-52
PMID: 14447167
-
Studies on the biosynthesis of cholesterol. XII. Synthesis of allyl pyrophosphates from mevalonate and their conversion into squalene with liver enzymes.
J Lipid Res. 1960 Jul;1:286-300
PMID: 13851061
-
Studies on the biosynthesis of cholesterol. XV. Mechanism of squalene biosynthesis from farnesyl pyrophosphate and from mevalonate.
J Biol Chem. 1961 Jul;236:1934-47
PMID: 13737104
-
Protein measurement with the Folin phenol reagent.
J Biol Chem. 1951 Nov;193(1):265-75
PMID: 14907713
-
The low-density lipoprotein pathway and its relation to atherosclerosis.
Annu Rev Biochem. 1977;46:897-930
PMID: 197883
-
Synthesis of ubiquinone and cholesterol in human fibroblasts: regulation of a branched pathway.
Arch Biochem Biophys. 1979 Jan;192(1):86-99
PMID: 219777
-
Nonparticipation of 105,000 x g liver supernatant or sterol carrier protein in the enzymatic conversion of farnesyl pyrophosphate to squalene by rat liver microsomes.
J Biol Chem. 1978 Aug 10;253(15):5470-5
PMID: 209043
-
Squalene synthetase. Solubilization from yeast microsomes of a phospholipid-requiring enzyme.
J Biol Chem. 1978 Jul 10;253(13):4574-83
PMID: 350878
-
Induction of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in human fibroblasts incubated with compactin (ML-236B), a competitive inhibitor of the reductase.
J Biol Chem. 1978 Feb 25;253(4):1121-8
PMID: 624722
-
Solubilization and purification of trans-farnesyl pyrophosphate-squalene synthetase.
J Biol Chem. 1971 Dec 25;246(24):7690-6
PMID: 4400077
-
The effect of sterol carrier protein on squalene synthesis.
Biochem Biophys Res Commun. 1972 Jan 31;46(2):470-5
PMID: 4400440
-
Hog liver squalene synthetase: the partial purification of the particulate enzyme and kinetic analysis of the reaction.
Arch Biochem Biophys. 1972 Sep;152(1):28-35
PMID: 4403691
-
Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured human fibroblasts. Comparison of cells from a normal subject and from a patient with homozygous familial hypercholesterolemia.
J Biol Chem. 1974 Feb 10;249(3):789-96
PMID: 4359767
-
The effects of fasting, refeeding, and time of day on the levels of enzymes effecting the conversion of -hydroxy- -methylglutaryl-coenzyme A to squalene.
J Biol Chem. 1972 May 25;247(10):3014-22
PMID: 4337504
-
A new intermediate in the biosynthesis of squalene.
J Biol Chem. 1966 Jul 10;241(13):3233-6
PMID: 4287912
-
Biochemistry of polyisoprenoid biosynthesis.
Annu Rev Biochem. 1976;45:113-42
PMID: 9026
-
Receptor-mediated control of cholesterol metabolism.
Science. 1976 Jan 16;191(4223):150-4
PMID: 174194
-
Suppression of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity and inhibition of growth of human fibroblasts by 7-ketocholesterol.
J Biol Chem. 1974 Nov 25;249(22):7306-14
PMID: 4436312
-
Sites of control of hepatic cholesterol biosynthesis.
J Lipid Res. 1966 Sep;7(5):698-707
PMID: 5971049