The mechanism of heparin stimulation of rat adipocyte lipoprotein lipase

Free fat cells and stromal-vascular cells were prepared from rat adipose tissue by incubation with collagenase. NH4OH-NH4Cl extracts of acetone-ether powders prepared from fat cells contained lipoprotein lipase activity but extracts of stromal-vascular cells did not. Intact fat cells released lipopr...

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Main Authors: R.L. Patten, C.H. Hollenberg
Format: Article
Language:English
Published: Elsevier 1969-07-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520430639
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spelling doaj-e434555ae7f345369759eb017465ae672021-04-24T05:55:16ZengElsevierJournal of Lipid Research0022-22751969-07-01104374382The mechanism of heparin stimulation of rat adipocyte lipoprotein lipaseR.L. Patten0C.H. Hollenberg1The McGill University Medical Clinic, The Montreal General Hospital, Montreal, Quebec, CanadaThe McGill University Medical Clinic, The Montreal General Hospital, Montreal, Quebec, CanadaFree fat cells and stromal-vascular cells were prepared from rat adipose tissue by incubation with collagenase. NH4OH-NH4Cl extracts of acetone-ether powders prepared from fat cells contained lipoprotein lipase activity but extracts of stromal-vascular cells did not. Intact fat cells released lipoprotein lipase activity into incubation medium, but intact stromal-vascular cells did not. The lipoprotein lipase activity of the medium was increased when fat cells were incubated with heparin, and this was accompanied by a corresponding decrease in the activity of subsequently prepared fat cell extracts. Heparin did not release lipoprotein lipase activity from stromal-vascular cells.The lipoprotein lipase activity of NH4OH-NH4Cl extracts of fat cell acetone powders is increased by the presence of heparin during the assay. This increase is not due to preservation of enzyme activity, but to increased binding of lipoprotein lipase to chylomicrons. Protamine sulfate and sodium chloride have little effect on the binding of lipoprotein lipase to chylomicrons, but they inhibit enzyme activity after binding to substrate has occurred. These inhibitors do, however, inhibit the stimulatory effect of heparin on enzyme-substrate binding.http://www.sciencedirect.com/science/article/pii/S0022227520430639enzyme-substrate bindingchylomicron-lipoprotein lipase bindingprotamine sulfatesodium chloride
collection DOAJ
language English
format Article
sources DOAJ
author R.L. Patten
C.H. Hollenberg
spellingShingle R.L. Patten
C.H. Hollenberg
The mechanism of heparin stimulation of rat adipocyte lipoprotein lipase
Journal of Lipid Research
enzyme-substrate binding
chylomicron-lipoprotein lipase binding
protamine sulfate
sodium chloride
author_facet R.L. Patten
C.H. Hollenberg
author_sort R.L. Patten
title The mechanism of heparin stimulation of rat adipocyte lipoprotein lipase
title_short The mechanism of heparin stimulation of rat adipocyte lipoprotein lipase
title_full The mechanism of heparin stimulation of rat adipocyte lipoprotein lipase
title_fullStr The mechanism of heparin stimulation of rat adipocyte lipoprotein lipase
title_full_unstemmed The mechanism of heparin stimulation of rat adipocyte lipoprotein lipase
title_sort mechanism of heparin stimulation of rat adipocyte lipoprotein lipase
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1969-07-01
description Free fat cells and stromal-vascular cells were prepared from rat adipose tissue by incubation with collagenase. NH4OH-NH4Cl extracts of acetone-ether powders prepared from fat cells contained lipoprotein lipase activity but extracts of stromal-vascular cells did not. Intact fat cells released lipoprotein lipase activity into incubation medium, but intact stromal-vascular cells did not. The lipoprotein lipase activity of the medium was increased when fat cells were incubated with heparin, and this was accompanied by a corresponding decrease in the activity of subsequently prepared fat cell extracts. Heparin did not release lipoprotein lipase activity from stromal-vascular cells.The lipoprotein lipase activity of NH4OH-NH4Cl extracts of fat cell acetone powders is increased by the presence of heparin during the assay. This increase is not due to preservation of enzyme activity, but to increased binding of lipoprotein lipase to chylomicrons. Protamine sulfate and sodium chloride have little effect on the binding of lipoprotein lipase to chylomicrons, but they inhibit enzyme activity after binding to substrate has occurred. These inhibitors do, however, inhibit the stimulatory effect of heparin on enzyme-substrate binding.
topic enzyme-substrate binding
chylomicron-lipoprotein lipase binding
protamine sulfate
sodium chloride
url http://www.sciencedirect.com/science/article/pii/S0022227520430639
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