ABC1 promotes engulfment of apoptotic cells and transbilayer redistribution of phosphatidylserine.

被引:445
作者
Hamon, Y
Broccardo, C
Chambenoit, O
Luciani, MF
Toti, F
Chaslin, S
Freyssinet, JM
Devaux, PF
McNeish, J
Marguet, D
Chimini, G [1 ]
机构
[1] CNRS Marseille Luminy, INSERM, Ctr Immunol, F-13288 Marseille, France
[2] Univ Strasbourg 1, INSERM, U143, F-67085 Strasbourg, France
[3] Univ Strasbourg 1, Inst Hematol & Immunol, F-67085 Strasbourg, France
[4] Inst Biol Physicochim, F-75005 Paris, France
[5] Pfizer Inc, Cent Res, Groton, CT 06340 USA
关键词
D O I
10.1038/35017029
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
ATP-binding-cassette transporter 1 (ABC1) has been implicated in processes related to membrane-lipid turnover. Here, using in vivo Toss-of-function and in vitro gain-of-function models, we show that ABC1 promotes Ca2+-induced exposure of phosphatidylserine at the membrane, as determined by a prothrombinase assay, membrane microvesiculation and measurement of transbilayer redistribution of spin-labelled phospholipids. That ABC1 promotes engulfment of dead cells is shown by the impaired ability of ABC1-deficient macrophages to engulf apoptotic preys and by the acquisition of phagocytic behaviour by ABC1 transfectants. Release of membrane phospholipids and cholesterol to apo-AI, the protein core of the cholesterol-shuttling high-density lipoprotein (HDL) particle, is also ABC1-dependent. We propose that both the efficiency of apoptotic-cell engulfment and the efflux of cellular lipids depend on ABC1-induced perturbation of membrane phosphatidylserine turnover. Transient local exposure of anionic phospholipids in the outer membrane leaflet may be sufficient to alter the general properties of the membrane and thus influence discrete physiological functions.
引用
收藏
页码:399 / 406
页数:8
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