Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptor

LPL mediates the uptake of lipoproteins into different cell types independent of its catalytic activity. The mechanism of this process and its physiological relevance are not clear. Taking into account the importance of the endothelial barrier for lipoprotein uptake, in vitro studies with primary ao...

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Main Authors: Britta Loeffler, Joerg Heeren, Mareike Blaeser, Herbert Radner, Daniel Kayser, Birol Aydin, Martin Merkel
Format: Article
Language:English
Published: Elsevier 2007-02-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520436648
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author Britta Loeffler
Joerg Heeren
Mareike Blaeser
Herbert Radner
Daniel Kayser
Birol Aydin
Martin Merkel
author_facet Britta Loeffler
Joerg Heeren
Mareike Blaeser
Herbert Radner
Daniel Kayser
Birol Aydin
Martin Merkel
author_sort Britta Loeffler
collection DOAJ
description LPL mediates the uptake of lipoproteins into different cell types independent of its catalytic activity. The mechanism of this process and its physiological relevance are not clear. Taking into account the importance of the endothelial barrier for lipoprotein uptake, in vitro studies with primary aortic endothelial cells from wild-type and low density lipoprotein receptor (LDLR)-deficient (LDLR−/−) mice were performed. Addition of LPL almost doubled the uptake of LDL into wild-type cells. However, there was virtually no LPL-mediated change of LDL uptake into LDLR−/− cells. Upregulation of LDLR by lipoprotein-deficient serum/lovastatin in wild-type cells resulted in a 7-fold increase of LPL-mediated LDL uptake. Uptake of chylomicron remnants was not affected by LDLR expression. In proteoglycan-deficient cells, LPL did not increase the uptake of lipoproteins. The physiological relevance of this pathway was studied in mice that were both LDLR−/− and transgenic for catalytically inactive LPL in muscle. In the presence of LDLR, inactive LPL reduced LDL cholesterol significantly (13–24%). In the absence of LDLR, LDL cholesterol was not affected by transgenic LPL. Metabolic studies showed that in the presence of LDLR, LPL increased the muscular uptake of LDL by 77%. In the absence of LDLR, transgenic LPL did not augment LDL uptake. Chylomicron uptake was not affected by the LDLR genotype. We conclude that LPL-mediated cellular uptake of LDL, but not of chylomicrons, is dependent on the presence of both LDLR and proteoglycans.
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spelling doaj.art-fb96e7f1b7f040c4ae20b598f420ce542022-12-21T22:07:44ZengElsevierJournal of Lipid Research0022-22752007-02-01482288298Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptorBritta Loeffler0Joerg Heeren1Mareike Blaeser2Herbert Radner3Daniel Kayser4Birol Aydin5Martin Merkel6Third Department of Internal Medicine, University Hospital Hamburg-Eppendorf, Hamburg, GermanyDepartment of Biochemistry and Molecular Cell Biology II, University Hospital Hamburg-Eppendorf, Hamburg, GermanyThird Department of Internal Medicine, University Hospital Hamburg-Eppendorf, Hamburg, GermanyInstitute of Pathology, Johannes-Gutenberg-University, Mainz, GermanyThird Department of Internal Medicine, University Hospital Hamburg-Eppendorf, Hamburg, GermanyThird Department of Internal Medicine, University Hospital Hamburg-Eppendorf, Hamburg, GermanyThird Department of Internal Medicine, University Hospital Hamburg-Eppendorf, Hamburg, GermanyLPL mediates the uptake of lipoproteins into different cell types independent of its catalytic activity. The mechanism of this process and its physiological relevance are not clear. Taking into account the importance of the endothelial barrier for lipoprotein uptake, in vitro studies with primary aortic endothelial cells from wild-type and low density lipoprotein receptor (LDLR)-deficient (LDLR−/−) mice were performed. Addition of LPL almost doubled the uptake of LDL into wild-type cells. However, there was virtually no LPL-mediated change of LDL uptake into LDLR−/− cells. Upregulation of LDLR by lipoprotein-deficient serum/lovastatin in wild-type cells resulted in a 7-fold increase of LPL-mediated LDL uptake. Uptake of chylomicron remnants was not affected by LDLR expression. In proteoglycan-deficient cells, LPL did not increase the uptake of lipoproteins. The physiological relevance of this pathway was studied in mice that were both LDLR−/− and transgenic for catalytically inactive LPL in muscle. In the presence of LDLR, inactive LPL reduced LDL cholesterol significantly (13–24%). In the absence of LDLR, LDL cholesterol was not affected by transgenic LPL. Metabolic studies showed that in the presence of LDLR, LPL increased the muscular uptake of LDL by 77%. In the absence of LDLR, transgenic LPL did not augment LDL uptake. Chylomicron uptake was not affected by the LDLR genotype. We conclude that LPL-mediated cellular uptake of LDL, but not of chylomicrons, is dependent on the presence of both LDLR and proteoglycans.http://www.sciencedirect.com/science/article/pii/S0022227520436648lipidscholesterolatherosclerosisendotheliumtransportlow density lipoprotein
spellingShingle Britta Loeffler
Joerg Heeren
Mareike Blaeser
Herbert Radner
Daniel Kayser
Birol Aydin
Martin Merkel
Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptor
Journal of Lipid Research
lipids
cholesterol
atherosclerosis
endothelium
transport
low density lipoprotein
title Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptor
title_full Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptor
title_fullStr Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptor
title_full_unstemmed Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptor
title_short Lipoprotein lipase-facilitated uptake of LDL is mediated by the LDL receptor
title_sort lipoprotein lipase facilitated uptake of ldl is mediated by the ldl receptor
topic lipids
cholesterol
atherosclerosis
endothelium
transport
low density lipoprotein
url http://www.sciencedirect.com/science/article/pii/S0022227520436648
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