Cholesterol efflux potential of sera from mice expressing human cholesteryl ester transfer protein and/or human apolipoprotein Al

被引:41
作者
Atger, V
delaLleraMoya, M
Bamberger, M
Francone, O
Cosgrove, P
Tall, A
Walsh, A
Moatti, N
Rothblat, G
机构
[1] MED COLL PENN,DEPT BIOCHEM,PHILADELPHIA,PA 19129
[2] HOP BROUSSAIS,PARIS,FRANCE
[3] HAHNEMANN UNIV,PHILADELPHIA,PA 19129
[4] PFIZER INC,GROTON,CT 06340
[5] COLUMBIA UNIV,NEW YORK,NY 10027
[6] ROCKEFELLER UNIV,NEW YORK,NY 10021
关键词
transgenic mice; lipoprotein; tissue culture cells; lipids; sterols;
D O I
10.1172/JCI118326
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The ability of whole serum to promote cell cholesterol efflux and the relationships between apoprotein and lipoprotein components of human serum and efflux have been investigated previously (de la Llera Moya, M., V. Atger. J. L. Paul, N. Fournier, N. Moatti, P. Giral, K. E. Friday, and G. H. Rothblat, 1994. Arterioscler, Thromb. 14:1056-1065), We have now used this experimental system to study the selective effects of two human lipoprotein-related proteins, apoprotein AI (ape AI) and cholesteryl ester transfer protein (CETP) on cell cholesterol efflux, when these proteins are expressed in transgenic mice, The percent efflux values for cholesterol released in 4 h from Fu5AH donor cells to 5% sera from the different groups of mice were in the order: background = human ape AI transgenic (HuAITg) > human CETP transgenic (HuCETPTg) > human ape AI and CETP transgenic (HuAICETPTg) much greater than apo AI knockout mice, In each group of mice a strong, positive correlation (r(2) ranging from 0.64 to 0.76) was found between efflux and HDL cholesterol concentrations, The slopes of these regression lines differed between groups of mice, indicating that the cholesterol acceptor efficiencies of the sera differed among groups, These differences in relative efficiencies can explain why cholesterol efflux was not proportional to the different HDL levels in the various groups of mice, We can conclude that: (a) HDL particles from HuAITg mice are less efficient as cholesterol accepters than HDL from the background mice; (b) despite a lower average efflux due to lower HDL cholesterol concentrations, HDL particles are more efficient in the HuCETPTg mice than in the background mice; and (c) the coexpression of both human ape AI and CETP improves the efficiency of HDL particles in the HuAICETPTg mice when compared with the HuAITg mice, We also demonstrated that the esterification of the free cholesterol released from the cells by lecithin cholesterol acyltransferase in the serum was reduced in the HuAITg and AI knockout mice, whereas it was not different from background values in the two groups of mice expressing human CETP.
引用
收藏
页码:2613 / 2622
页数:10
相关论文
共 55 条
  • [1] AGELLON LB, 1991, J BIOL CHEM, V266, P10796
  • [2] CELLULAR CHOLESTEROL ESTER ACCUMULATION INDUCED BY FREE CHOLESTEROL-RICH LIPID DISPERSIONS
    ARBOGAST, LY
    ROTHBLAT, GH
    LESLIE, MH
    COOPER, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (10) : 3680 - 3684
  • [3] 2-DIMENSIONAL ELECTROPHORESIS OF PLASMA-LIPOPROTEINS - RECOGNITION OF NEW APO-A-I-CONTAINING SUBPOPULATIONS
    ASZTALOS, BF
    SLOOP, CH
    WONG, L
    ROHEIM, PS
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1169 (03) : 291 - 300
  • [4] ATGER V, 1991, CLIN CHEM, V37, P1149
  • [5] BIELICKI JK, 1992, J LIPID RES, V33, P1699
  • [6] BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
  • [7] LIPOPROTEIN METABOLISM IN THE MACROPHAGE - IMPLICATIONS FOR CHOLESTEROL DEPOSITION IN ATHEROSCLEROSIS
    BROWN, MS
    GOLDSTEIN, JL
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1983, 52 : 223 - 261
  • [8] BURKEY BF, 1995, J LIPID RES, V36, P1463
  • [9] CHOLESTEROL EXCRETION BY TISSUE CULTURE CELLS - EFFECT OF SERUM LIPIDS
    BURNS, CH
    ROTHBLAT, GH
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 176 (03) : 616 - &
  • [10] EARLY INCORPORATION OF CELL-DERIVED CHOLESTEROL INTO PRE-BETA-MIGRATING HIGH-DENSITY LIPOPROTEIN
    CASTRO, GR
    FIELDING, CJ
    [J]. BIOCHEMISTRY, 1988, 27 (01) : 25 - 29