Function and clinical significance of platelet-derived microparticles

被引:136
作者
Nomura, S [1 ]
机构
[1] Kansai Med Univ, Dept Internal Med 1, Osaka 5708507, Japan
关键词
microparticle; procoagulant activity; high shear stress; flow cytometry; clinical disorder;
D O I
10.1007/BF02982082
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Microparticles released from platelets (PMPs) may play a role in the normal hemostatic response to vascular injury because they demonstrate prothrombinase activity. PMPs were first observed as released vesicles from platelets following adhesion to vessel walls, and flow cytometry is now the most widely used method for studying PMPs. PMPs are thought to play a role in clinical disease because they express phospholipids that function as procoagulants. High shear stress can initiate both platelet aggregation and shedding of procoagulant-containing PMP, suggesting that PMP generation by high shear stress occurs in small diseased arteries and arterioles under various clinical conditions. In addition, the possibility that PMPs evoke cellular responses in their immediate microenvironments has recently been suggested. Despite many interesting findings, the significance of PMPs in various clinical conditions remains controversial. For example, it is not known whether PMPs found in peripheral blood vessels cause thrombosis, or if they are the results of thrombosis. There has been some question about whether the PMPs found in thromboses are consumed locally, meaning that PMPs circulating in the peripheral blood are not functionally important. Currently, the number of clinical disorders associated with elevated PMPs is increasing. Int J Hematol. 2001:74:397-404. (C) 2001 The Japanese Society of Hematology.
引用
收藏
页码:397 / 404
页数:8
相关论文
共 115 条
[71]   PLATELET-DERIVED MICROPARTICLES MAY INFLUENCE THE DEVELOPMENT OF ATHEROSCLEROSIS IN DIABETES-MELLITUS [J].
NOMURA, S ;
SUZUKI, M ;
KATSURA, K ;
XIE, GL ;
MIYAZAKI, Y ;
MIYAKE, T ;
KIDO, H ;
KAGAWA, H ;
FUKUHARA, S .
ATHEROSCLEROSIS, 1995, 116 (02) :235-240
[72]   Significance of chemokines and activated platelets in patients with diabetes [J].
Nomura, S ;
Shouzu, A ;
Omoto, S ;
Nishikawa, M ;
Fukuhara, S .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2000, 121 (03) :437-443
[73]   Platelet-derived microparticles in patients with arteriosclerosis obliterans: Enhancement of high shear-induced microparticle generation by cytokines [J].
Nomura, S ;
Imamura, A ;
Okuno, M ;
Kamiyama, Y ;
Fujimura, Y ;
Ikeda, Y ;
Fukuhara, S .
THROMBOSIS RESEARCH, 2000, 98 (04) :257-268
[74]   Relationship between platelet activation and cytokines in systemic inflammatory response syndrome patients with hematological malignancies [J].
Nomura, S ;
Kagawa, H ;
Ozaki, Y ;
Nagahama, M ;
Yoshimura, C ;
Fukuhara, S .
THROMBOSIS RESEARCH, 1999, 95 (05) :205-213
[75]   High-shear-stress-induced activation of platelets and microparticles enhances expression of cell adhesion molecules in THP-1 and endothelial cells [J].
Nomura, S ;
Tandon, NN ;
Nakamura, T ;
Cone, J ;
Fukuhara, S ;
Kambayashi, J .
ATHEROSCLEROSIS, 2001, 158 (02) :277-287
[76]   ANTIPHOSPHOLIPID ANTIBODIES BIND TO PLATELET MICROPARTICLES IN IDIOPATHIC (AUTOIMMUNE) THROMBOCYTOPENIC PURPURA [J].
NOMURA, S ;
YANABU, M ;
FUKUROI, T ;
KIDO, H ;
KAWAKATSU, T ;
YAMAGUCHI, K ;
SUZUKI, M ;
KOKAWA, T ;
YASUNAGA, K .
ANNALS OF HEMATOLOGY, 1992, 65 (01) :46-49
[77]   EFFECTS OF TICLOPIDINE ON MONOCLONAL ANTI-CD9 ANTIBODY-INDUCED PLATELET-AGGREGATION AND MICROPARTICLE GENERATION [J].
NOMURA, S ;
NAGATA, H ;
SUZUKI, M ;
IWATA, K ;
KAWAKATSU, T ;
KIDO, H ;
FUKUROI, T ;
YAMAGUCHI, K ;
YANABU, M ;
SOGA, T ;
KOKAWA, T ;
YASUNAGA, K .
THROMBOSIS RESEARCH, 1992, 65 (01) :95-104
[78]   ANTIPLATELET AUTOANTIBODY-RELATED MICROPARTICLES IN PATIENTS WITH IDIOPATHIC (AUTOIMMUNE) THROMBOCYTOPENIC PURPURA [J].
NOMURA, S ;
YANABU, M ;
KIDO, H ;
FUKUROI, T ;
YAMAGUCHI, K ;
SOGA, T ;
NAGATA, H ;
KOKAWA, T ;
YASUNAGA, K .
ANNALS OF HEMATOLOGY, 1991, 62 (04) :103-107
[79]   MICROPARTICLE GENERATION DURING INVITRO PLATELET ACTIVATION BY ANTI-CD9 MURINE MONOCLONAL-ANTIBODIES [J].
NOMURA, S ;
NAGATA, H ;
SUZUKI, M ;
KONDO, K ;
OHGA, S ;
KAWAKATSU, T ;
KIDO, H ;
FUKUROI, T ;
YAMAGUCHI, K ;
IWATA, K ;
YANABU, M ;
SOGA, T ;
KOKAWA, T ;
YASUNAGA, K .
THROMBOSIS RESEARCH, 1991, 62 (05) :429-439
[80]  
Nomura S, 1996, HAEMOSTASIS, V26, P31