A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro

A synthetic LDL (sLDL) has been prepared by combining a lipid microemulsion with amphipathic peptides containing the apoprotein B receptor domain. The biological properties of sLDL have been investigated using the U937 in vitro cell proliferation assay. sLDL exhibits a concentration dependent and sa...

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Main Authors: G. Baillie, M.D. Owens, G.W. Halbert
Format: Article
Language:English
Published: Elsevier 2002-01-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520301887
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spelling doaj-faca6f8e58fd462bb4007f1a17ef5ee92021-04-27T04:38:25ZengElsevierJournal of Lipid Research0022-22752002-01-014316973A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitroG. Baillie0M.D. Owens1G.W. Halbert2Department of Pharmaceutical Sciences, Strathclyde Institute for Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, G4 0NR, United KingdomDepartment of Pharmaceutical Sciences, Strathclyde Institute for Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, G4 0NR, United KingdomDepartment of Pharmaceutical Sciences, Strathclyde Institute for Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, G4 0NR, United KingdomA synthetic LDL (sLDL) has been prepared by combining a lipid microemulsion with amphipathic peptides containing the apoprotein B receptor domain. The biological properties of sLDL have been investigated using the U937 in vitro cell proliferation assay. sLDL exhibits a concentration dependent and saturable stimulation of U937 proliferation. By utilizing different amphipathic peptides, variable proliferation is achieved, indicating a specific interaction between sLDL and the U937 LDL receptor are possible. U937 proliferation is reduced by the addition of an anti-LDL receptor antibody, indicating that sLDL is assimilated via the LDL receptor pathway. The behavior of sLDL mimics that of native LDL, and this approach represents a viable technique for the production of an sLDL particle on a large scale for research and general application. —Baillie, G., M. D. Owens, and G. W. Halbert. A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro. J. Lipid Res. 2002. 43: 69–73.http://www.sciencedirect.com/science/article/pii/S0022227520301887U937low density lipoproteinamphipathic peptideapoBsynthetic LDLphosphate-buffered saline
collection DOAJ
language English
format Article
sources DOAJ
author G. Baillie
M.D. Owens
G.W. Halbert
spellingShingle G. Baillie
M.D. Owens
G.W. Halbert
A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro
Journal of Lipid Research
U937
low density lipoprotein
amphipathic peptide
apoB
synthetic LDL
phosphate-buffered saline
author_facet G. Baillie
M.D. Owens
G.W. Halbert
author_sort G. Baillie
title A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro
title_short A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro
title_full A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro
title_fullStr A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro
title_full_unstemmed A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro
title_sort synthetic low density lipoprotein particle capable of supporting u937 proliferation in vitro
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 2002-01-01
description A synthetic LDL (sLDL) has been prepared by combining a lipid microemulsion with amphipathic peptides containing the apoprotein B receptor domain. The biological properties of sLDL have been investigated using the U937 in vitro cell proliferation assay. sLDL exhibits a concentration dependent and saturable stimulation of U937 proliferation. By utilizing different amphipathic peptides, variable proliferation is achieved, indicating a specific interaction between sLDL and the U937 LDL receptor are possible. U937 proliferation is reduced by the addition of an anti-LDL receptor antibody, indicating that sLDL is assimilated via the LDL receptor pathway. The behavior of sLDL mimics that of native LDL, and this approach represents a viable technique for the production of an sLDL particle on a large scale for research and general application. —Baillie, G., M. D. Owens, and G. W. Halbert. A synthetic low density lipoprotein particle capable of supporting U937 proliferation in vitro. J. Lipid Res. 2002. 43: 69–73.
topic U937
low density lipoprotein
amphipathic peptide
apoB
synthetic LDL
phosphate-buffered saline
url http://www.sciencedirect.com/science/article/pii/S0022227520301887
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