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
收藏
页码:1 / 8
页数:8
相关论文
共 65 条
[11]   ISOLATION AND CHARACTERIZATION OF CHINESE HAMSTER OVARY CELL MUTANTS DEFECTIVE IN INTRACELLULAR LOW-DENSITY LIPOPROTEIN CHOLESTEROL TRAFFICKING [J].
CADIGAN, KM ;
SPILLANE, DM ;
CHANG, TY .
JOURNAL OF CELL BIOLOGY, 1990, 110 (02) :295-308
[12]  
CHANG CCY, 1993, J BIOL CHEM, V268, P20747
[13]  
Christian AE, 1997, J LIPID RES, V38, P2264
[14]   Analysis of chimeric receptors shows that multiple distinct functional activities of scavenger receptor, class B, type I (SR-BI), are localized to the extracellular receptor domain [J].
Connelly, MA ;
de la Llera-Moya, M ;
Monzo, P ;
Yancey, PG ;
Drazul, D ;
Stoudt, G ;
Fournier, N ;
Klein, SM ;
Rothblat, GH ;
Williams, DL .
BIOCHEMISTRY, 2001, 40 (17) :5249-5259
[15]   ESSENTIAL DIFFERENCES IN CHOLESTERYL ESTER METABOLISM BETWEEN HUMAN MONOCYTE-DERIVED AND J774 MACROPHAGES - EVIDENCE AGAINST THE PRESENCE OF HORMONE-SENSITIVE LIPASE IN HUMAN MACROPHAGES [J].
CONTRERAS, JA ;
LASUNCION, MA .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (03) :443-452
[16]   Relationship between donor age and the replicative lifespan of human cells in culture: A reevaluation [J].
Cristofalo, VJ ;
Allen, RG ;
Pignolo, RJ ;
Martin, BG ;
Beck, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10614-10619
[17]  
DAVIDSON WS, 1994, J BIOL CHEM, V269, P22975
[18]   EFFECTS OF ACCEPTOR PARTICLE-SIZE ON THE EFFLUX OF CELLULAR FREE-CHOLESTEROL [J].
DAVIDSON, WS ;
RODRIGUEZA, WV ;
LUNDKATZ, S ;
JOHNSON, WJ ;
ROTHBLAT, GH ;
PHILLIPS, MC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (29) :17106-17113
[19]  
de la Llera-Moya M, 1999, J LIPID RES, V40, P575
[20]   A CELL-CULTURE SYSTEM FOR SCREENING HUMAN SERUM FOR ABILITY TO PROMOTE CELLULAR CHOLESTEROL EFFLUX - RELATIONS BETWEEN SERUM COMPONENTS AND EFFLUX, ESTERIFICATION, AND TRANSFER [J].
DELALLERAMOYA, M ;
ATGER, V ;
PAUL, JL ;
FOURNIER, N ;
MOATTI, N ;
GIRAL, P ;
FRIDAY, KE ;
ROTHBLAT, G .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (07) :1056-1065