3-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileum
The localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase, E.C. 1.1.1.34) in the villous and crypt cells of the small intestine was accomplished after separating these cells from the mucosal layer by sequential dissociation in a “dual-buffer“ system. Consistent separatio...
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Elsevier
1977-11-01
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Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520415901 |
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doaj-3f7ba813485d4683a0403e4dfc2ad3c72021-04-24T05:53:44ZengElsevierJournal of Lipid Research0022-22751977-11-011867227333-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileumJ L Merchant0R A Heller1Department of Biological Sciences and the Department of Medicine, School of Medicine, Stanford University, Stanford, CA 94305Department of Biological Sciences and the Department of Medicine, School of Medicine, Stanford University, Stanford, CA 94305The localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase, E.C. 1.1.1.34) in the villous and crypt cells of the small intestine was accomplished after separating these cells from the mucosal layer by sequential dissociation in a “dual-buffer“ system. Consistent separation was demonstrated by using the marker enzymes alkaline phosphatase, specific to the villous cell, and thymidine kinase, specific to the crypt cell. Cells obtained were 95–100% viable, and no relative difference in lability was observed, as evidenced by the equal distribution of acid phosphatase. This method of cell separation was an improvement over the “scraping” technique which damaged cells severely and produced villous preparations that contained little or no reductase activity. The HMG-CoA reductase specific activity in whole cell homogenates of the ileal villi was 0.47 and of the crypts was 0.27 nmol/min per mg of protein, considerably higher values than have been reported earlier. Also in comparison to the crypts, the villi incorporated 1.5-fold more [14C]-acetate into sterols, a ratio similar to that describing the distribution of HMG-CoA reductase in the two cell populations. These results unequivocally establish that the villi have higher HMG-CoA reductase activity than the crypts and confirm an earlier report from this laboratory that the villi are a major site of sterol synthesis. The sterol bio-synthetic capacity of the small intestine was highest in the ileum and decreased towards the jejunum. The HMG-CoA reductase specific activity of the ileum averaged 0.30 and that of the jejunum 0.10 nmol/min per mg of protein; however, the cholesterol content of the ileum was slightly lower than the jejunum. These results are discussed to suggest the possibility that the sterol content of the ileum may largely be due to in situ synthesis.http://www.sciencedirect.com/science/article/pii/S0022227520415901HMG-CoA reductasesterol synthesisjejunum |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
J L Merchant R A Heller |
spellingShingle |
J L Merchant R A Heller 3-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileum Journal of Lipid Research HMG-CoA reductase sterol synthesis jejunum |
author_facet |
J L Merchant R A Heller |
author_sort |
J L Merchant |
title |
3-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileum |
title_short |
3-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileum |
title_full |
3-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileum |
title_fullStr |
3-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileum |
title_full_unstemmed |
3-Hydroxy-3-methylglutaryl coenzyme A reductase in isolated villous and crypt cells of the rat ileum |
title_sort |
3-hydroxy-3-methylglutaryl coenzyme a reductase in isolated villous and crypt cells of the rat ileum |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
1977-11-01 |
description |
The localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase, E.C. 1.1.1.34) in the villous and crypt cells of the small intestine was accomplished after separating these cells from the mucosal layer by sequential dissociation in a “dual-buffer“ system. Consistent separation was demonstrated by using the marker enzymes alkaline phosphatase, specific to the villous cell, and thymidine kinase, specific to the crypt cell. Cells obtained were 95–100% viable, and no relative difference in lability was observed, as evidenced by the equal distribution of acid phosphatase. This method of cell separation was an improvement over the “scraping” technique which damaged cells severely and produced villous preparations that contained little or no reductase activity. The HMG-CoA reductase specific activity in whole cell homogenates of the ileal villi was 0.47 and of the crypts was 0.27 nmol/min per mg of protein, considerably higher values than have been reported earlier. Also in comparison to the crypts, the villi incorporated 1.5-fold more [14C]-acetate into sterols, a ratio similar to that describing the distribution of HMG-CoA reductase in the two cell populations. These results unequivocally establish that the villi have higher HMG-CoA reductase activity than the crypts and confirm an earlier report from this laboratory that the villi are a major site of sterol synthesis. The sterol bio-synthetic capacity of the small intestine was highest in the ileum and decreased towards the jejunum. The HMG-CoA reductase specific activity of the ileum averaged 0.30 and that of the jejunum 0.10 nmol/min per mg of protein; however, the cholesterol content of the ileum was slightly lower than the jejunum. These results are discussed to suggest the possibility that the sterol content of the ileum may largely be due to in situ synthesis. |
topic |
HMG-CoA reductase sterol synthesis jejunum |
url |
http://www.sciencedirect.com/science/article/pii/S0022227520415901 |
work_keys_str_mv |
AT jlmerchant 3hydroxy3methylglutarylcoenzymeareductaseinisolatedvillousandcryptcellsoftheratileum AT raheller 3hydroxy3methylglutarylcoenzymeareductaseinisolatedvillousandcryptcellsoftheratileum |
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