Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.

In order to study the effects of very low density (VLDL) and low density (LDL) lipoproteins on the activity and specificity of lecithin:cholesterol acyltransferase (LCAT), we determined the molecular species of cholesteryl esters (CE) synthesized in the plasma from three abetalipoproteinemic (ABL) p...

Full description

Bibliographic Details
Main Authors: PV Subbaiah, B Banerji, RE Gregg, JD Bagdade
Format: Article
Language:English
Published: Elsevier 1990-05-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520427920
_version_ 1818927373447331840
author PV Subbaiah
B Banerji
RE Gregg
JD Bagdade
author_facet PV Subbaiah
B Banerji
RE Gregg
JD Bagdade
author_sort PV Subbaiah
collection DOAJ
description In order to study the effects of very low density (VLDL) and low density (LDL) lipoproteins on the activity and specificity of lecithin:cholesterol acyltransferase (LCAT), we determined the molecular species of cholesteryl esters (CE) synthesized in the plasma from three abetalipoproteinemic (ABL) patients, before and after supplementation with normal VLDL or LDL. The patients' plasma had significantly lower concentration of 18:2 CE and higher concentrations of 16:0 CE and 18:1 CE compared to normal plasma. Incubation of ABL plasma with [4-14C]cholesterol at 37 degrees C and the subsequent analysis of labeled CE formed by high performance liquid chromatography revealed that the major species formed was 16:0 CE (34% of total label), whereas similar incubation of the d greater than 1.063 g/ml fraction of normal plasma resulted in the formation of predominantly 18:2 CE (45% of total label). Addition of normal VLDL or LDL to ABL plasma stimulated the total LCAT activity by 30-80% and normalized the CE species synthesized. The LCAT activity of a normal d greater than 1.063 g/ml fraction also was stimulated by the normal VLDL or LDL, but there was no alteration in the species of CE formed. Most of the CE synthesized was found in the added VLDL or LDL with both ABL and normal plasma, indicating that the CE transfer (CET) activity was not affected in ABL plasma. These results suggest that while the VLDL and LDL are required for the maximal activity of LCAT, the species of CE formed are primarily determined by the molecular species composition of phosphatidylcholine in the plasma.
first_indexed 2024-12-20T03:11:59Z
format Article
id doaj.art-738818db47194605a0c313d066a3a9ab
institution Directory Open Access Journal
issn 0022-2275
language English
last_indexed 2024-12-20T03:11:59Z
publishDate 1990-05-01
publisher Elsevier
record_format Article
series Journal of Lipid Research
spelling doaj.art-738818db47194605a0c313d066a3a9ab2022-12-21T19:55:26ZengElsevierJournal of Lipid Research0022-22751990-05-01315927932Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.PV Subbaiah0B Banerji1RE Gregg2JD Bagdade3Department of Medicine, Rush Medical College, Chicago, IL 60612.Department of Medicine, Rush Medical College, Chicago, IL 60612.Department of Medicine, Rush Medical College, Chicago, IL 60612.Department of Medicine, Rush Medical College, Chicago, IL 60612.In order to study the effects of very low density (VLDL) and low density (LDL) lipoproteins on the activity and specificity of lecithin:cholesterol acyltransferase (LCAT), we determined the molecular species of cholesteryl esters (CE) synthesized in the plasma from three abetalipoproteinemic (ABL) patients, before and after supplementation with normal VLDL or LDL. The patients' plasma had significantly lower concentration of 18:2 CE and higher concentrations of 16:0 CE and 18:1 CE compared to normal plasma. Incubation of ABL plasma with [4-14C]cholesterol at 37 degrees C and the subsequent analysis of labeled CE formed by high performance liquid chromatography revealed that the major species formed was 16:0 CE (34% of total label), whereas similar incubation of the d greater than 1.063 g/ml fraction of normal plasma resulted in the formation of predominantly 18:2 CE (45% of total label). Addition of normal VLDL or LDL to ABL plasma stimulated the total LCAT activity by 30-80% and normalized the CE species synthesized. The LCAT activity of a normal d greater than 1.063 g/ml fraction also was stimulated by the normal VLDL or LDL, but there was no alteration in the species of CE formed. Most of the CE synthesized was found in the added VLDL or LDL with both ABL and normal plasma, indicating that the CE transfer (CET) activity was not affected in ABL plasma. These results suggest that while the VLDL and LDL are required for the maximal activity of LCAT, the species of CE formed are primarily determined by the molecular species composition of phosphatidylcholine in the plasma.http://www.sciencedirect.com/science/article/pii/S0022227520427920
spellingShingle PV Subbaiah
B Banerji
RE Gregg
JD Bagdade
Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.
Journal of Lipid Research
title Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.
title_full Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.
title_fullStr Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.
title_full_unstemmed Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.
title_short Molecular species of cholesteryl esters formed in abetalipoproteinemia: effect of apoprotein B-containing lipoproteins.
title_sort molecular species of cholesteryl esters formed in abetalipoproteinemia effect of apoprotein b containing lipoproteins
url http://www.sciencedirect.com/science/article/pii/S0022227520427920
work_keys_str_mv AT pvsubbaiah molecularspeciesofcholesterylestersformedinabetalipoproteinemiaeffectofapoproteinbcontaininglipoproteins
AT bbanerji molecularspeciesofcholesterylestersformedinabetalipoproteinemiaeffectofapoproteinbcontaininglipoproteins
AT regregg molecularspeciesofcholesterylestersformedinabetalipoproteinemiaeffectofapoproteinbcontaininglipoproteins
AT jdbagdade molecularspeciesofcholesterylestersformedinabetalipoproteinemiaeffectofapoproteinbcontaininglipoproteins