Increased plasma HDL cholesterol levels and biliary cholesterol excretion in hamster by LCAT overexpression

被引:22
作者
Zhang, AH
Gao, S
Fan, JL
Huang, W
Zhao, TQ
Liu, G
机构
[1] Peking Univ, Minist Educ, Inst Cardiovasc Sci, Beijing 100083, Peoples R China
[2] Peking Univ, Minist Educ, Key Lab Mol Chem, Beijing 100083, Peoples R China
[3] Univ Tsukuba, Inst Basic Med Sci, Dept Pathol, Cardiovasc Dis Lab, Tsukuba, Ibaraki 3058575, Japan
关键词
lecithin cholesterol acyltransferase; high density; lipoprotein; bile acid; adenovirils; gene; hamster;
D O I
10.1016/j.febslet.2004.06.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lecithin cholesterol acyltransferase (LCAT) is a key enzyme in the metabolism of high density lipoprotein (HDL), which has been found inversely correlated with atherosclerosis. Adenovirus mediated overexpression of human LCAT (hLCAT) in hamsters resulted in increased levels of plasma total cholesterol, HDL cholesterol, phospholipids and enlarged particle size of HDL. It also increased cholesterol and total bile acid concentrations in bile. Hepatic mRNA level of cholesterol 7alpha hydroxylase increased 2.7-fold in hamsters. However, such effects were not observed in mice in a parallel experiment. This study suggests that overexpression of hLCAT in hamsters facilitated reverse cholesterol transport. Similar metabolic changes in humans might modify atherogenic risk. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 29
页数:5
相关论文
共 27 条
[1]   Long-term stable expression of human apolipoprotein A-I mediated by helper-dependent adenovirus gene transfer inhibits atherosclerosis progression and remodels atherosclerotic plaques in a mouse model of familial hypercholesterolemia [J].
Belalcazar, LM ;
Merched, A ;
Carr, B ;
Oka, K ;
Chen, KH ;
Pastore, L ;
Beaudet, A ;
Chan, L .
CIRCULATION, 2003, 107 (21) :2726-2732
[2]   High plasma HDL concentrations associated with enhanced atherosclerosis in transgenic mice overexpressing lecithin-cholesteryl acyltransferase [J].
Berard, AM ;
Foger, B ;
Remaley, A ;
Shamburek, R ;
Vaisman, BL ;
Talley, G ;
Paigen, B ;
Hoyt, RF ;
Marcovina, S ;
Brewer, HB ;
SantamarinaFojo, S .
NATURE MEDICINE, 1997, 3 (07) :744-749
[3]  
Boden WE, 2000, AM J CARDIOL, V86, p19L
[4]  
Brousseau ME, 1999, J LIPID RES, V40, P365
[5]  
Brousseau ME, 1997, J LIPID RES, V38, P2537
[6]  
CHEN CH, 1982, J LIPID RES, V23, P680
[7]   Transgenic rabbit models for biomedical research: Current status, basic methods and future perspectives [J].
Fan, JL ;
Challah, M ;
Watanabe, T .
PATHOLOGY INTERNATIONAL, 1999, 49 (07) :583-594
[8]   Real-time PCR quantification of full-length and exon 11 spliced BRCA1 transcripts in human breast cancer cell lines [J].
Favy, DA ;
Lafarge, S ;
Rio, P ;
Vissac, C ;
Bignon, YJ ;
Bernard-Gallon, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 274 (01) :73-78
[9]   Cholesteryl ester transfer protein corrects dysfunctional high density lipoproteins and reduces aortic atherosclerosis in lecithin cholesterol acyltransferase transgenic mice [J].
Föger, B ;
Chase, M ;
Amar, MJ ;
Vaisman, BL ;
Shamburek, RD ;
Paigen, B ;
Furchart-Najib, J ;
Paiz, JA ;
Koch, CA ;
Hoyt, RF ;
Brewer, HB ;
Santamarina-Fojo, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) :36912-36920
[10]  
FOLCH J, 1957, J BIOL CHEM, V226, P497