Cellular cholesterol flux studies: methodological considerations

被引:80
作者
Rothblat, GH [1 ]
de la Llera-Moya, M [1 ]
Favari, E [1 ]
Yancey, PG [1 ]
Kellner-Weibel, G [1 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Sch Med,Abramson Res Ctr, Dept Pediat,Div Gastroenterol & Nutr, Philadelphia, PA 19104 USA
关键词
cholesterol flux; tissue culture; methods; SR-B1; ABCA1; lipoproteins; reverse cholesterol transport;
D O I
10.1016/S0021-9150(01)00713-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reverse cholesterol transport (RCT) is the process in which peripheral cells release cholesterol to an extracellular acceptor Such as high-density lipoprotein (HDL) which then mediates cholesterol delivery to the liver for excretion. RCT represents a physiological mechanism by which peripheral tissues Lire protected against excessive accumulation of cholesterol. The first step in RCT is the interaction of the cell with lipoprotein particles, a process that results in both the cellular uptake and release of cholesterol. The various components of this cholesterol flux call be viewed as efflux, influx and net flux. Experimental protocols for measuring each of these components of cholesterol flux are very different, and a number of considerations are required to design experimental approaches for the quantitation of flux parameters. Although many flux studies have been conducted ill the past, the recent discoveries of the scavenger receptor B1 (SR-B1) and ATP binding cassette 1 (ABCA1), which mediate the movement of cholesterol between cells and extracellular acceptors, has led to increased interest in studies Of Cellular cholesterol flux. The aim of this review is to present a discussion of the methodological considerations that should be evaluated during the design and analysis of cellular cholesterol flux experiments. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
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页码:1 / 8
页数:8
相关论文
共 65 条
[1]   Characterization of apolipoprotein-mediated HDL generation induced by cAMP in a murine macrophage cell line [J].
Abe-Dohmae, S ;
Suzuki, S ;
Wada, Y ;
Aburatani, H ;
Vance, DE ;
Yokoyama, S .
BIOCHEMISTRY, 2000, 39 (36) :11092-11099
[2]   Identification of scavenger receptor SR-BI as a high density lipoprotein receptor [J].
Acton, S ;
Rigotti, A ;
Landschulz, KT ;
Xu, SZ ;
Hobbs, HH ;
Krieger, M .
SCIENCE, 1996, 271 (5248) :518-520
[3]   MUTATIONS AT THE LYSOSOMAL ACID CHOLESTERYL ESTER HYDROLASE GENE LOCUS IN WOLMAN-DISEASE [J].
ANDERSON, RA ;
BYRUM, RS ;
COATES, PM ;
SANDO, GN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (07) :2718-2722
[4]   Effects of different dietary cholesterol concentrations on lipoprotein plasma concentrations and on cholesterol efflux from Fu5AH cells [J].
Blanco-Molina, A ;
Castro, G ;
Martín-Escalante, D ;
Bravo, D ;
López-Miranda, J ;
Castro, P ;
López-Segura, F ;
Fruchart, JC ;
Ordovás, JM ;
Pérez-Jiménez, F .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1998, 68 (05) :1028-1033
[5]   The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease [J].
Bodzioch, M ;
Orsó, E ;
Klucken, T ;
Langmann, T ;
Böttcher, L ;
Diederich, W ;
Drobnik, W ;
Barlage, S ;
Büchler, C ;
Porsch-Özcürümez, M ;
Kaminski, WE ;
Hahmann, HW ;
Oette, K ;
Rothe, G ;
Aslanidis, C ;
Lackner, KJ ;
Schmitz, G .
NATURE GENETICS, 1999, 22 (04) :347-351
[6]   The correlation of ATP-binding cassette 1 mRNA levels with cholesterol efflux from various cell lines [J].
Bortnick, AE ;
Rothblat, GH ;
Stoudt, G ;
Hoppe, KL ;
Royer, LJ ;
McNeish, J ;
Francone, OL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (37) :28634-28640
[7]   REGULATION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE-ACTIVITY IN HUMAN FIBROBLASTS BY LIPOPROTEINS [J].
BROWN, MS ;
DANA, SE ;
GOLDSTEIN, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (07) :2162-2166
[8]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[9]   REGULATION OF ACTIVITY OF LOW-DENSITY LIPOPROTEIN RECEPTOR IN HUMAN FIBROBLASTS [J].
BROWN, MS ;
GOLDSTEIN, JL .
CELL, 1975, 6 (03) :307-316
[10]   Mammalian acyl-CoA: cholesterol acyltransferases [J].
Buhman, KF ;
Accad, M ;
Farese, RV .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2000, 1529 (1-3) :142-154