P-glycoprotein and 'lipid rafts': some ambiguous mutual relationships (floating on them, building them or meeting them by chance?)

被引:102
作者
Orlowski, S. [1 ]
Martin, S.
Escargueil, A.
机构
[1] CEA Saclay, CNRS, Dept Biol Joliot Curie, Serv Biophys Fonct Membranaires, F-91191 Gif Sur Yvette, France
[2] CEA Saclay, CNRS, URA 2096, F-91191 Gif Sur Yvette, France
关键词
P-glycoprotein; multidrug resistance; drug transport; lipid translocase; cholesterol; sphingolipids; lipid rafts; lipid traffic;
D O I
10.1007/s00018-005-5554-9
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
P-glycoprotein (P-gp) is an active membrane transporter responsible for cell detoxification against numerous amphiphilic compounds, leading to multidrug resistance in tumor cells. It displays entangled connections with its membrane environment since it recognizes its substrates within the cytosolic leaflet and it also translocates some endogenous lipids to the exoplasmic leaflet. Regarding its relationships with membrane microdomains, 'Cylipid rafts', a literature analysis concludes that (i) P-gp also exists in rafts and non-raft membrane domains, depending on the cell considered, the experimental conditions and the method used to test it; (ii) cholesterol has a positive influence on P-gp function, and this may be a direct effect of the free cholesterol present in membrane or an indirect effect mediated by the cholesterol-enriched microdomains; (iii) when present in rafts, P-gp interacts with protein partners regulating its activity; (iv) P-gp is a lipid translocase that handles the raft-constituting lipids with particular efficiency, and it also influences membrane trafficking in the cell.
引用
收藏
页码:1038 / 1059
页数:22
相关论文
共 210 条
[61]  
Gouazé V, 2004, MOL CANCER THER, V3, P633
[62]   Cytoprotective effect of glucosylceramide synthase inhibition against daunorubicin-induced apoptosis in human leukemic cell lines [J].
Grazide, S ;
Terrisse, AD ;
Lerouge, S ;
Laurent, G ;
Jaffrézou, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (18) :18256-18261
[63]   Methyl-beta-cyclodextrin in HL-60 parental and multidrug-resistant cancer cell lines: effect on the cytotoxic activity and intracellular accumulation of doxorubicin [J].
Grosse, PY ;
Bressolle, F ;
Pinguet, F .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1997, 40 (06) :489-494
[64]   Ceramide and cell death receptor clustering [J].
Gulbins, E ;
Grassmé, H .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1585 (2-3) :139-145
[65]   ABC1 promotes engulfment of apoptotic cells and transbilayer redistribution of phosphatidylserine. [J].
Hamon, Y ;
Broccardo, C ;
Chambenoit, O ;
Luciani, MF ;
Toti, F ;
Chaslin, S ;
Freyssinet, JM ;
Devaux, PF ;
McNeish, J ;
Marguet, D ;
Chimini, G .
NATURE CELL BIOLOGY, 2000, 2 (07) :399-406
[66]   Cholesterol depletion induces large scale domain segregation in living cell membranes [J].
Hao, MM ;
Mukherjee, S ;
Maxfield, FR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (23) :13072-13077
[67]   IS THE MULTIDRUG TRANSPORTER A FLIPPASE [J].
HIGGINS, CF ;
GOTTESMAN, MM .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (01) :18-21
[68]   Rafts as missing link between multidrug resistance and sphingolipid metabolism [J].
Hinrichs, JWJ ;
Klappe, K ;
Kok, JW .
JOURNAL OF MEMBRANE BIOLOGY, 2005, 203 (02) :57-64
[69]   ATP-binding cassette transporters are enriched in non-caveolar detergent-insoluble glycosphingolipid-enriched membrane domains (DIGs) in human multidrug-resistant cancer cells [J].
Hinrichs, JWJ ;
Klappe, K ;
Hummel, I ;
Kok, JW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (07) :5734-5738
[70]   CHARACTERIZATION OF CELLULAR LIPIDS IN DOXORUBICIN-SENSITIVE AND DOXORUBICIN-RESISTANT P388 MOUSE LEUKEMIA-CELLS [J].
HOLLERAN, WM ;
DEGREGORIO, MW ;
GANAPATHI, R ;
WILBUR, JR ;
MACHER, BA .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1986, 17 (01) :11-15