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At least 1,027 records · Page 57Linked to original sources
PubMed1982

Increased cholesterol esterification in rat liver microsomes in purified non-specific phospholipid transfer protein.

The effect of the non-specific phospholipid transfer protein purified from rat liver on the activity of acyl-CoA:cholesterol acyltransferase (EC 2.3.1.26) in rat liver microsomes was studied. The activity of cholesterol acyltransferase was measured from the rate of incorporation of [1-14C] oleoyl-CoA into cholesteryl oleate. Activity was stimulated by preincubation by the microsomes with the non-specific phospholipid transfer protein alone, but most effectively when vesicles consisting of phosphatidylcholine/cholesterol (molar ratio 1:1) also were present in the preincubation mixture. Preincubation with vesicles consisting of only phosphatidylcholine or phosphatidylcholine/phosphatidylethanolamine (molar ratio 1:1) had no effect. The stimulating effect is dependent on transfer protein and vesicle concentration and on the length of preincubation. Treatment of the transfer protein with N-ethylmaleimide abolished its effect on cholesterol ester formation. Preincubation of the microsomes with transfer protein and phosphatidylcholine/cholesterol vesicles containing radioactively labeled cholesterol shows that exogenous cholesterol is converted readily to cholesterol ester. The data are explained by the ability of non-specific phospholipid transfer protein to effect net transfer of cholesterol to those microsomes that contain cholesterol acyltransferase. Enlargement of the cholesterol substrate pool would then give rise to stimulation of the cholesterol acyltransferase activity. This study suggests a role for the transfer protein in modulating cholesterol metabolism by its ability to transport cholesterol between membranes.

Acyl Coenzyme A↗
PubMed1984

Effect of K+ depolarization on the synthesis of prostaglandins and hydroxyeicosatetra(5,8,11,14)enoic acids (HETE) in the rat retina. Evidence for esterification of 12-HETE in lipids.

[14C]Arachidonic acid is metabolized to prostaglandins and hydroxyeicosatetraenoic acids in the rat retina. After intravitreal injection of [14C]arachidonic acid, 25% of the injected radiolabel was recovered in the retinal lipids. Phosphatidylcholine and phosphatidylinositol were most actively labeled; however, all glycerolipids incorporated arachidonic acid. The synthesis of prostaglandins E2, F2 alpha, D2, 6-keto-F1 alpha, thromboxane B2 and hydroxyeicosatetraenoic acids was measured by high-performance liquid chromatography. The identity of 12-HETE was confirmed by gas chromatography-mass spectrometry. Incubation of prelabeled retinas in vitro promoted the release of [14C]arachidonic acid from glycerolipids. A 12-fold increase in the synthesis of hydroxyeicosatetraenoic acids occurred with no change in the synthesis of prostaglandins. Incubation in a depolarizing medium (45 mM K+) resulted in a selective increase in hydroxyeicosatetraenoic acids, an effect that was blocked by nordihydroguaiaretic acid (1 microM) and eicosatetraynoic acid (10 microM). 12-[3H8]Hydroxyeicosatetraenoic acid, intravitreally injected, was incorporated into retinal lipids with a distribution similar to arachidonic acid. When retinas labeled with 12-[3H8]hydroxyeicosatetraenoic acid were incubated, there was a large release of the incorporated radioactivity, and metabolism to other products with the chromatographic properties of dihydroxyeicosatetraenoic acids. The release of 12-hydroxyeicosatetraenoic acid was not affected by depolarizing conditions (45 mM K+); however, the conversion of 12-hydroxyeicosatetraenoic acid to dihydroxy isomers was stimulated by K+. These experiments demonstrate active pathways for the generation of eicosanoids in the rat retina that are sensitive to membrane depolarization and lipoxygenase inhibitors.

Animals↗
PubMed1984

Regulation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase and cholesterol synthesis and esterification during the first cell cycle of liver regeneration.

The regenerating rat liver provides a unique in vivo synchronized system for study of the interrelationships between mevalonate and sterol metabolism during the cell cycle. The regulation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, cholesterol synthesis and acyl coenzyme A: cholesterol acyltransferase during the first cell cycle was investigated. At 8 h postoperative and prior to onset of DNA synthesis or S phase, cholesterol synthesis was depressed in the regenerating liver relative to that in sham-operated controls. This suppression was observed whether assayed in vitro with liver homogenates utilizing radiolabeled acetate, mevalonate or water or in vivo with tritium water. In contrast, at this time point, 3-hydroxy-3-methylglutaryl-CoA reductase activity was increased in microsomes prepared both in the presence and absence of NaF. By 24 h, well into S phase and approaching mitosis, reductase activity and cholesterol synthesis both approached levels observed in the sham-operated control animals. There were no detectable changes in acyl-CoA: cholesterol acyltransferase activity at any time point. Thus, at the 8 h time point, the regulation of the three processes appeared uncoupled. The increased levels of in vitro expressed 3-hydroxy-3-methylglutaryl-CoA reductase activity compared with the decrease in the rate of both cholesterol and squalene biosynthesis suggested diversion of mevalonate into products other than squalene or sterols. We propose that this may reflect the needs of the cell for a nonsterol metabolite of mevalonate necessary for entry of cells into S phase.

Animals↗
PubMed1994

The esterification of cholesterol in the liver of the chick embryo.

The development of the chick embryo was characterised by the accumulation of large droplets of lipid in the cytoplasm of the embryonic liver, as revealed by electron microscopy. Analysis of the lipid composition of the livers indicated that this accumulation resulted from a dramatic increase in the cholesteryl ester content of the tissue during the the latter part of the embryonic period. This lipid is apparently derived from yolk cholesterol and may be taken up by the liver in the form of lipoprotein remnants. Significant levels of acyl-CoA: cholesterol acyltransferase (ACAT) activity were expressed in the liver throughout the second half of the developmental period, and this activity was maximal at the time when lipid transfer from the yolk was most intensive. The activity of microsomal cholesterol ester hydrolase (CEH) was very low throughout development, and no CEH activity was detected in the cytosolic fraction. In addition, substantial amounts of a cytosolic protein which inhibits CEH activity were present. Thus the relative activities of these enzymic systems are consistent with the net accumulation of cholesteryl ester which occurs in the liver during development.

Animals↗
PubMed1996

Disparate effects of oxidation on plasma acyltransferase activities: inhibition of cholesterol esterification but stimulation of transesterification of oxidized phospholipids.

Oxidation of lipoproteins results in the formation of several polar phospholipids with pro-inflammatory and pro-atherogenic properties. To examine the possible role of lecithin/cholesterol acyltransferase (LCAT) in the metabolism of these oxidized phospholipids, we oxidized whole plasma with either Cu(2+) or a free-radical generator, and determined the various activities of LCAT. Oxidation caused a reduction in plasma phosphatidylcholine (PC), an increase in a short-chain polar PC (SCP-PC), and an inhibition of the transfer of long-chain acyl groups to cholesterol (LCAT activity) or to lyso PC (lysolecithin acyltransferase (LAT) I activity). However, the transfer of short-chain acyl groups from SCP-PC to lyso PCLAT II activity) was stimulated several fold, in direct correlation with the degree of oxidation. LAT II activity was not stimulated by oxidation in LCAT-deficient plasma, showing that it is carried out by LCAT. Oxidized normal plasma exhibited low LCAT activity even in the presence of exogenous proteoliposome substrate, indicating that the depletion of substrate PC was not responsible for the loss of activity. Oxidation of isolated LDL or HDL abolished their ability to support LCAT and LAT I activities of exogenous enzyme, but promoted the LAT II activity. Purified LCAT lost its LCAT and LAT I functions, but not its LAT II function, when oxidized in vitro. These results show that while oxidation of plasma causes a loss of LCAT's ability to transfer long-chain acyl groups, its ability to transfer short-chain acyl groups, from SCP-PC is retained, and even stimulated, suggesting that LCAT may have a physiological role in the metabolism of oxidized PC in plasma.

Adult↗
PubMed1976

Esterification of J chain and its effect on electrophoretic mobility in sodium dodecyl sulfate polyacrylamide gels.

Sodium dodecyl sulfate polyacrylamide gel electrophoresis yields mobilities indicative of molecular weights of approximately 27 000 for human J chain and approximately 14 000 for nurse shark J chain, in contrast to values of approximately 15 500 and approximately 12 200, respectively, obtained by other methods. The relatively high content of acidic amino acids of human J chain as compared to nurse shark J chain suggested that the greater error in the sodium dodecyl sulfate determined molecular weight for human J chain may be due to a charge anomaly. The overall net negative charge on human J chain was decreased by forming methyl esters of the carboxyl groups, resulting in a sodium dodecyl sulfate determined molecular weight of approximately 17 700. Methylated nurse shark J chain did not show a significant difference in sodium dodecyl sulfate electrophoretic mobility from the non-methylated form. These results form the basis for a possible explanation of an occasional artifact in a widely used analytical method.

Animals↗
PubMed1987

Dibutyryl-cyclic AMP inhibits cholesterol esterification in J 774 monocyte-like cells.

The effect of dibutyryl-cyclic AMP (dbcAMP) and theophylline was investigated on oleic acid incorporation into cholesteryl esters and triacylglycerols in the mouse monocyte-macrophage cell line J 774. 24h pretreatment of macrophages with dbcAMP decreased cholesteryl ester formation in a dose-dependent manner (about 4 fold reduction for dbcAMP 10(-4)M + theophylline 10(-3)M), while oleic acid incorporation into triacylglycerols was markedly (2 to 3 fold) enhanced. The catabolism of acetylated LDL was only slightly affected (about 15-20% reduction with dbcAMP 5 X 10(-4)M + theophylline 10(-3)M). Acyl Coenzyme A: cholesterol-O-acyl-transferase activity, measured in vitro on cell homogenates, was reduced in dbcAMP-treated cells, whereas diacylglycerol acyltransferase activity was increased. These results suggest that cyclic AMP can modulate cholesteryl ester and triacylglycerol formation in macrophages, and that these metabolisms are inversely regulated. Agents which increase cyclic AMP intracellular level could be of interest for reducing cholesteryl ester accumulation in macrophages.

Acyltransferases↗