2008
DOI: 10.1016/j.plipres.2008.04.002
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Sterol regulators of cholesterol homeostasis and beyond: The oxysterol hypothesis revisited and revised

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Cited by 189 publications
(175 citation statements)
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“…Lanosterol, the first sterol intermediate in cholesterol biosynthesis, is synthesized via condensation of isoprene to squalene and subsequent oxidation of squalene to MOS, followed by cyclization of MOS. 24,25-EC is generated de novo by a shunt of the cholesterol biosynthetic pathway through synthesis of 2,3;22,23-diepoxysqualene (DOS) from MOS (29). When CHO-K1 cells were metabolically labeled with [ 14 C]acetate, synthesis of MOS, cholesterol, and 24,25-EC was apparently reduced upon elevation of plasmalogens (Fig.…”
Section: Cell Line Treatmentmentioning
confidence: 99%
“…Lanosterol, the first sterol intermediate in cholesterol biosynthesis, is synthesized via condensation of isoprene to squalene and subsequent oxidation of squalene to MOS, followed by cyclization of MOS. 24,25-EC is generated de novo by a shunt of the cholesterol biosynthetic pathway through synthesis of 2,3;22,23-diepoxysqualene (DOS) from MOS (29). When CHO-K1 cells were metabolically labeled with [ 14 C]acetate, synthesis of MOS, cholesterol, and 24,25-EC was apparently reduced upon elevation of plasmalogens (Fig.…”
Section: Cell Line Treatmentmentioning
confidence: 99%
“…Cholesterol Esterification-Cells were labeled with 1 Ci of [1][2][3][4][5][6][7][8][9][10][11][12][13][14] C]palmitate (specific activity 56.0 mCi/mmol; American Radiolabeled Chemicals) for 4 h during treatment. Lipid extracts were analyzed for cholesteryl [ 14 C]esters by thin layer chromatography (TLC) followed by phosphorimaging, as described previously (29).…”
Section: Methodsmentioning
confidence: 99%
“…In addition, certain oxysterols and intermediates in cholesterol synthesis also participate in cholesterol homeostasis (12), for example, by inhibiting SREBP activation (13) and by accelerating the Insigdependent proteasomal degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR), another key cholesterol biosynthetic enzyme (14,15).…”
mentioning
confidence: 99%
“…Oxysterols reportedly diminished the rate of cholesterol biosynthesis being a potent inhibitor even at 10-9 M, though cholesterol itself was weakly inhibitory at 10-5 M [6]. It is believed that the presence of a large excess of cholesterol (100 fold) in vivo reduced oxysterol binding affinity to nuclear receptors, whereas high affinity binding to receptors were noted in vitro [7]. .…”
Section: Introductionmentioning
confidence: 99%