Platelets release active matrix metalloproteinase-2 in vivo in humans at a site of vascular injury:: lack of inhibition by aspirin

被引:44
作者
Falcinelli, Emanuela [1 ]
Giannini, Silvia [1 ]
Boschetti, Enrico [1 ]
Gresele, Paolo [1 ]
机构
[1] Univ Perugia, Div Int & Cardiovasc Med, Dept Internal Med, I-06126 Perugia, Italy
关键词
aspirin; bleeding time; matrix metalloproteinase-2; platelets;
D O I
10.1111/j.1365-2141.2007.06632.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
When stimulated in vitro, human platelets release matrix metalloproteinase-2 (MMP-2) that, in turn, potentiates platelet activation. The present study investigated if MMP-2 is released from activated platelets in vivo in humans and whether aspirin inhibits this release. MMP-2 levels were measured by zymography, immunoblotting, flow-cytometry and an activity assay system, in plasma prepared from blood emerging from a skin wound inflicted for the measurement of the bleeding time (shed blood) and simultaneously from venous blood in 27 healthy human volunteers. In a subgroup, the same measurements were carried out before and 1 h after aspirin intake. MMP-2 was significantly higher in shed blood than in venous blood and increased progressively, consistent with ongoing platelet activation. A significant correlation was evident between platelet number and MMP-2 in shed blood; platelet MMP-2 content in shed blood was lower than that of platelets in venous blood. The level of active MMP-2 released by activated platelets in vivo was within the range of concentrations that potentiate platelet activation. Aspirin did not reduce MMP-2 release in vivo. In conclusion, MMP-2 is released from platelets in vivo in humans at a localised site of vessel wall damage in amounts sufficient to potentiate platelet aggregation; aspirin does not reduce this release.
引用
收藏
页码:221 / 230
页数:10
相关论文
共 37 条
[1]  
ABRAMS CS, 1990, BLOOD, V75, P128
[2]   Determination of gelatinase-A (MMP-2) activity using a novel immunocapture assay [J].
Capper, SJ ;
Verheijen, J ;
Smith, L ;
Sully, M ;
Visser, H ;
Hanemaaijer, R .
INHIBITION OF MATRIX METALLOPROTEINASES: THERAPEUTIC APPLICATIONS, 1999, 878 :487-490
[3]  
Ciferri S, 2000, THROMB HAEMOSTASIS, V83, P157
[4]   Defective platelet β-N-acetyl hexosaminidase content and release in chronic myeloproliferative disorders [J].
Emiliani, C ;
Ciferri, S ;
Mencarelli, S ;
Mezzasoma, AM ;
Momi, S ;
Orlacchio, A ;
Gresele, P .
PLATELETS, 2006, 17 (01) :20-29
[5]   Intraplatelet signaling mechanisms of the priming effect of matrix metal loproteinase-2 on platelet aggregation [J].
Falcinelli, E ;
Guglielmini, G ;
Torti, M ;
Gresele, P .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2005, 3 (11) :2526-2535
[6]   The role of collagen in thrombosis and hemostasis [J].
Farndale, RW ;
Sixma, JJ ;
Barnes, MJ ;
De Groot, PG .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (04) :561-573
[7]   Differential regulation of platelet aggregation by matrix metalloproteinases-9 and-2 [J].
Fernandez-Patron, C ;
Martinez-Cuesta, MA ;
Salas, E ;
Sawicki, G ;
Wozniak, M ;
Radomski, MW ;
Davidge, ST .
THROMBOSIS AND HAEMOSTASIS, 1999, 82 (06) :1730-1735
[8]   Matrix metalloproteinases in vascular remodeling and atherogenesis - The good, the bad, and the ugly [J].
Galis, ZS ;
Khatri, JJ .
CIRCULATION RESEARCH, 2002, 90 (03) :251-262
[9]   Outside-in signals delivered by matrix metalloproteinase-1 regulate platelet function [J].
Galt, SW ;
Lindemann, S ;
Allen, L ;
Medd, DJ ;
Falk, JM ;
McIntyre, TM ;
Prescott, SM ;
Kraiss, LW ;
Zimmerman, GA ;
Weyrich, AS .
CIRCULATION RESEARCH, 2002, 90 (10) :1093-1099
[10]   ROLE OF PROAGGREGATORY AND ANTIAGGREGATORY PROSTAGLANDINS IN HEMOSTASIS - STUDIES WITH COMBINED THROMBOXANE SYNTHASE INHIBITION AND THROMBOXANE RECEPTOR ANTAGONISM [J].
GRESELE, P ;
ARNOUT, J ;
DECKMYN, H ;
HUYBRECHTS, E ;
PIETERS, G ;
VERMYLEN, J .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (05) :1435-1445