Microparticles in cardiovascular diseases

被引:502
作者
VanWijk, MJ
VanBavel, E
Sturk, A
Nieuwland, R
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Clin Chem, NL-1100 DD Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Obstet & Gynaecol, NL-1100 DD Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Med Phys, NL-1100 DD Amsterdam, Netherlands
关键词
coronary disease; endothelial function; hemostasis; platelets; thrombosis;
D O I
10.1016/S0008-6363(03)00367-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Microparticles are membrane vesicles released from many different cell types. There are two mechanisms that can result in their formation, cell activation and apoptosis. In these two mechanisms, different pathways are involved in microparticle generation. Microparticle generation seems to be a well regulated process. Microparticles vary in size, phospholipid and protein composition. They have a potent pro-inflammatory effect, promote coagulation and affect vascular function. Since these processes are all involved in the pathogenesis of cardiovascular disease and circulating microparticle numbers are altered in many cardiovascular diseases, a role for microparticles in the pathogenesis of cardiovascular diseases is likely. Although hard evidence for a role of microparticles in cardiovascular diseases at present is still only limited, new evidence is accumulating rapidly to support this theory. Elucidation of the microparticle composition and the mechanisms involved in exertion of their effects will supply this evidence and enable us to develop additional intervention strategies for prevention and treatment of cardiovascular diseases. (C) 2003 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:277 / 287
页数:11
相关论文
共 92 条
[31]  
HAMILTON KK, 1990, J BIOL CHEM, V265, P3809
[32]   Shear-induced platelet activation and platelet microparticle formation at blood flow conditions as in arteries with a severe stenosis [J].
Holme, PA ;
Orvim, U ;
Hamers, MJAG ;
Solum, NO ;
Brosstad, FR ;
Barstad, RM ;
Sakariassen, KS .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (04) :646-653
[33]   Oxidized membrane vesicles and blebs from apoptotic cells contain biologically active oxidized phospholipids that induce monocyte-endothelial interactions [J].
Huber, J ;
Vales, A ;
Mitulovic, G ;
Blumer, M ;
Schmid, R ;
Witztum, JL ;
Binder, BR ;
Leitinger, N .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (01) :101-107
[34]   Elevated levels of circulating procoagulant microparticles in patients with paroxysmal nocturnal hemoglobinuria and aplastic anemia [J].
Hugel, B ;
Socié, G ;
Vu, T ;
Toti, F ;
Gluckman, E ;
Freyssinet, JM ;
Scrobohaci, ML .
BLOOD, 1999, 93 (10) :3451-3456
[35]   Morphological analysis of microparticle generation in heparin-induced thrombocytopenia [J].
Hughes, M ;
Hayward, CPM ;
Warkentin, TE ;
Horsewood, P ;
Chorneyko, KA ;
Kelton, JG .
BLOOD, 2000, 96 (01) :188-194
[36]  
ISSEKUTZ TB, 1981, AM J PATHOL, V103, P47
[37]  
Joop K, 2001, THROMB HAEMOSTASIS, V85, P810
[38]  
JY W, 1992, J LAB CLIN MED, V119, P334
[39]   Platelet microparticles bind, activate and aggregate neutrophils in vitro [J].
Jy, WC ;
Mao, WW ;
Horstman, LL ;
Tao, JG ;
Ahn, YS .
BLOOD CELLS MOLECULES AND DISEASES, 1995, 21 (22) :217-231
[40]   ELEVATED PLATELET MICROPARTICLES IN TRANSIENT ISCHEMIC ATTACKS, LACUNAR INFARCTS, AND MULTIINFARCT DEMENTIAS [J].
LEE, YJ ;
JY, W ;
HORSTMAN, LL ;
JANANIA, J ;
REYES, Y ;
KELLEY, RE ;
AHN, YS .
THROMBOSIS RESEARCH, 1993, 72 (04) :295-304