Surface exposure of phosphatidylserine in pathological cells

被引:625
作者
Zwaal, RFA [1 ]
Comfurius, P [1 ]
Bevers, EM [1 ]
机构
[1] Maastricht Univ, Cardiovasc Res Inst Maastricht CARIM, Dept Biochem, NL-6200 MD Maastricht, Netherlands
关键词
membrane asymmetry; lipid scramblase; aminophospholipid translocase; apoptosis; blood coagulation; erythrocytes; platelets;
D O I
10.1007/s00018-005-4527-3
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
The asymmetric phospholipid distribution in plasma membranes is normally maintained by energy-dependent lipid transporters that translocate different phospholipids from one monolayer to the other against their respective concentration gradients. When cells are activated, or enter apoptosis, lipid asymmetry can be perturbed by other lipid transporters (scramblases) that shuttle phospholipids non-specifically between the two monolayers. This exposes phosphatidylserine (PS) at the cells' outer surface. Since PS promotes blood coagulation, defective scramblase activity upon platelet stimulation causes a bleeding disorder (Scott syndrome). PS exposure also plays a pivotal role in the recognition and removal of apoptotic cells via a PS-recognizing receptor on phagocytic cells. Furthermore, expression of PS at the cell surface can occur in a wide variety of disorders. This review aims at highlighting how PS expression in different cells may complicate a variety of pathological conditions, including those that promote thromboembolic complications or produce aberrations in apoptotic cell removal.
引用
收藏
页码:971 / 988
页数:18
相关论文
共 214 条
[1]  
Allen JY, 1996, AM J REPROD IMMUNOL, V36, P81
[2]   Circulating platelet-derived microparticles with procoagulant activity may be a potential cause of thrombosis in uremic patients [J].
Ando, M ;
Iwata, A ;
Ozeki, Y ;
Tsuchiya, K ;
Akiba, T ;
Nihei, H .
KIDNEY INTERNATIONAL, 2002, 62 (05) :1757-1763
[3]   Current status and implications of autoimmune antiphospholipid antibodies in relation to thrombotic disease [J].
Arnout, J ;
Vermylen, J .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (05) :931-942
[4]   Masking of phosphatidylserine inhibits apoptotic cell engulfment and induces autoantibody production in mice [J].
Asano, K ;
Miwa, M ;
Miwa, K ;
Hanayama, R ;
Nagase, H ;
Nagata, S ;
Tanaka, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (04) :459-467
[5]   Relationship between hypercoagulable state and erythrocyte phosphatidylserine exposure in splenectomized haemoglobin E/β-thalassaemic patients [J].
Atichartakarn, V ;
Angchaisuksiri, P ;
Aryurachai, K ;
Onpun, S ;
Chuncharunee, S ;
Thakkinstian, A ;
Atamasirikul, K .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 118 (03) :893-898
[6]   Apoptotic-like mitochondrial events associated to phosphatidylserine exposure in blood platelets induced by local anaesthetics [J].
Augereau, O ;
Rossignol, R ;
DeGiorgi, F ;
Mazat, JP ;
Letellier, T ;
Dachary-Prigent, J .
THROMBOSIS AND HAEMOSTASIS, 2004, 92 (01) :104-113
[7]   RECONSTITUTION OF ATP-DEPENDENT AMINOPHOSPHOLIPID TRANSLOCATION IN PROTEOLIPOSOMES [J].
AULAND, ME ;
ROUFOGALIS, BD ;
DEVAUX, PF ;
ZACHOWSKI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) :10938-10942
[8]   Binding of annexin V to membrane products of lipid peroxidation [J].
Balasubramanian, K ;
Bevers, EM ;
Willems, GM ;
Schroit, AJ .
BIOCHEMISTRY, 2001, 40 (30) :8672-8676
[9]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[10]   Reactive oxygen species and phosphatidylserine externalization in murine sickle red cells [J].
Banerjee, T ;
Kuypers, FA .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 124 (03) :391-402