Phospholipid scramblase: An update

被引:188
作者
Bevers, Edouard M. [1 ]
Williamson, Patrick L. [2 ]
机构
[1] Maastricht Univ, Cardiovasc Res Inst Maastricht, Dept Biochem, NL-6200 MD Maastricht, Netherlands
[2] Amherst Coll, Dept Biol, Amherst, MA 01002 USA
关键词
Lipid asymmetry; Phosphatidylserine; Apoptosis; Scott syndrome; Plasma membrane; PLATELET PROCOAGULANT ACTIVITY; PERMEABILITY TRANSITION PORE; TRANSBILAYER LIPID MOVEMENT; RED-BLOOD-CELLS; PHOSPHATIDYLSERINE EXPOSURE; PLASMA-MEMBRANE; SCOTT-SYNDROME; AMINOPHOSPHOLIPID TRANSLOCASE; APOPTOTIC CELLS; BLEEDING DISORDER;
D O I
10.1016/j.febslet.2010.03.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The best understood consequence of the collapse of lipid asymmetry is exposure of phosphatidylserine (PS) in the external leaflet of the plasma membrane bilayer, where it is known to serve at least two major functions: providing a platform for development of the blood coagulation cascade and presenting the signal that induces phagocytosis of apoptotic cells. Lipid asymmetry is collapsed by activation of phospholipid scramblase(s) that catalyze bidirectional transbilayer movement of the major classes of phospholipid. The protein corresponding to this activity is not yet known. Observations on cells from patients with Scott syndrome, a rare hereditary bleeding disorder resulting from impaired lipid scrambling, have shown that there are multiple activation pathways that converge on scramblase activity. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2724 / 2730
页数:7
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