Mitochondrial biosynthesis of cholesterol in Leydig cells from rat testis |
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Authors: | O P Pignataro J P Radicella J C Calvo E H Charreau |
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Affiliation: | 1. Department of Zoology and Entomology, Colorado State University, Fort Collins, CO 80523 U.S.A.;2. Department of Biology. Queen''s University, Kingston, Ontario K7L 3N6 Canada |
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Abstract: | The subcellular location of some enzymes responsible for cholesterol biosynthesis was studied in metrizamide-purified rat Leydig cells. The highest activity of 3-hydroxy-3-methyl glutaryl coenzyme A reductase (HMG-CoA reductase), a key regulatory enzyme in the cholesterol pathway, was associated with highly enriched mitochondrial fractions with recovery of 62% of the total activity and was located on the inner membrane. A significant part of the activity (35%) was also present in the cytoplasm. The activity of this enzyme in the other subcellular fractions was negligible. The HMG-CoA synthase activity was also found almost entirely in the mitochondria (90%). Otherwise no detectable activity of HMG-CoA lyase was present in the subcellular fractions studied. Furthermore, cholesterol may be synthesized from acetyl-CoA inside the mitochondrion, since a significant incorporation (90%) of [14C]acetyl-CoA into digitonin-precipitable sterols was observed in this organelle and only 10% in the cytoplasmic fraction. The evidence strongly suggests that much of the cholesterol biosynthesis that takes place in Leydig cells is carried out within the mitochondria. |
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Keywords: | locust fat body juvenile hormone binding cytosol receptors hydroxyapatite BP binding protein DCC dextran-coated charcoal DFP diisopropyl phosphofluoridate DMSO dimethyl sulfoxide HAP hydroxyapatite JH-I JH-III LS low salt buffer PEG polyethylene glycol TTg Tris-thioglycerol buffer TTgM Tris-thioglycerol-magnesium buffer |
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