Comparative studies with surface plasmon resonance and free oscillation rheometry on the inhibition of platelets with cytochalasin E and monoclonal antibodies towards GPIIb/IIIa

被引:7
作者
Hansson, KM [1 ]
Tengvall, P
Lundström, I
Råndy, M
Lindahl, TL
机构
[1] Linkoping Univ Hosp, Dept Biomed & Surg, Div Clin Chem, SE-58185 Linkoping, Sweden
[2] Linkoping Univ, Div Appl Chem, Dept Phys & Measurement Technol, SE-58183 Linkoping, Sweden
[3] Linkoping Univ, Forum Scientum Grad Sch, SE-58183 Linkoping, Sweden
关键词
surface plasmon resonancc; free oscillation rheometry; whole blood coagulation; platelets;
D O I
10.1016/S0956-5663(02)00049-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In the haemostatic system a multitude of processes are intertwined in fine-tuned interactions that arrest bleeding, keep the circulatory system open, and the blood flowing. The occurrence of both surface and bulk interactions adds an additional dimension of complexity. These insights have led to the belief that global overall procedures can inform on the likely behaviour of the system in health and disease. Two sensing procedures: surface plasmon resonance (SPR), which senses surface interactions, and free oscillation rheometry (FOR), which senses interactions within the bulk, have been combined and evaluated. The contribution of blood cells, mainly platelets, to the SPR and FOR signals was explored by simultaneous SPR and FOR measurement during native whole blood coagulation, accelerated via the platelets through addition of SFLLRN peptide and inhibition of platelet aggregation with abciximab (ReoPro((R))) and of shape change with cytochalasin E. The SPR technique was found to be sensitive to inhibition of blood cell functions such as adhesion to and spreading on surfaces, as well as platelet aggregation. SPR seemed not to be directly sensitive to fibrin polymerisation in coagulating whole blood. The FOR technique detected the coagulation as a bulk phenomenon, i.e. the gelation of the blood due to Fibrin formation was detected. The combination of SPR and FOR may therefore be suitable for studies on blood cell functions during coagulation. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:761 / 771
页数:11
相关论文
共 22 条
[1]   SURFACE RECRUITMENT BUT NOT ACTIVATION OF INTEGRIN ALPHA(IIB)BETA(3) (GPIIB-IIIA) REQUIRES A FUNCTIONAL ACTIN CYTOSKELETON [J].
ADDO, JB ;
BRAY, PF ;
GRIGORYEV, D ;
FARADAY, N ;
GOLDSCHMIDTCLERMONT, PJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (09) :1466-1473
[2]  
BOHLIN L, 1998, Patent No. 9854475
[3]  
BOHLIN L, 1994, Patent No. 9408222
[4]   Networking in the hemostatic system - Integrin alpha(IIIb)beta(3) binds prothrombin and influences its activation [J].
Byzova, TV ;
Plow, EF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :27183-27188
[5]   The platelet cytoskeleton stabilizes the interaction between alpha(IIb)beta(3) and its ligand and induces selective movements of ligand-occupied integrin [J].
Fox, JEB ;
Shattil, SJ ;
KinloughRathbone, RL ;
Richardson, M ;
Packham, MA ;
Sanan, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (12) :7004-7011
[6]   INHIBITION OF ACTIN POLYMERIZATION IN BLOOD-PLATELETS BY CYTOCHALASINS [J].
FOX, JEB ;
PHILLIPS, DR .
NATURE, 1981, 292 (5824) :650-652
[7]  
FUKADA E, 1984, Biorheology, P9
[8]   Surface plasmon resonance (SPR) analysis of coagulation in whole blood with application in prothrombin time assay [J].
Hansson, KM ;
Vikinge, TP ;
Rånby, M ;
Tengvall, P ;
Lundström, I ;
Johansen, K ;
Lindahl, TL .
BIOSENSORS & BIOELECTRONICS, 1999, 14 (8-9) :671-682
[9]  
HANSSON KM, 2002, IN PRESS BIOSENS BIO
[10]   MINIMAL SEQUENCE REQUIREMENT OF THROMBIN RECEPTOR AGONIST PEPTIDE [J].
HUI, KY ;
JAKUBOWSKI, JA ;
WYSS, VL ;
ANGLETON, EL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 184 (02) :790-796