MMP-13 binds to platelet receptors αIIbβ3 and GPVI and impairs aggregation and thrombus formation.

Howes, Joanna-Marie and Pugh, Nicholas and Hamaia, Samir W. and Jung, Stephanie M. and Knäuper, Vera and Malcor, Jean-Daniel M. and Farndale, Richard W. (2018) MMP-13 binds to platelet receptors αIIbβ3 and GPVI and impairs aggregation and thrombus formation. Research and Practice in Thrombosis and Haemostasis, 2 (2). pp. 370-379. ISSN 2475-0379

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Official URL: https://doi.org/10.1002/rth2.12088

Abstract

Acute thrombotic syndromes lead to atherosclerotic plaque rupture with subsequent thrombus formation, myocardial infarction and stroke. Following rupture, flowing blood is exposed to plaque components, including collagen, which triggers platelet activation and aggregation. However, plaque rupture releases other components into the surrounding vessel which have the potential to influence platelet function and thrombus formation. OBJECTIVES. Here we sought to elucidate whether matrix metalloproteinase-13 (MMP-13), a collagenolytic metalloproteinase up–regulated in atherothrombotic and inflammatory conditions, affects platelet aggregation and thrombus formation. RESULTS. We demonstrate that MMP-13 is able to bind to platelet receptors alphaIIbbeta3 (αIIbβ3) and platelet glycoprotein (GP)VI. The interactions between MMP-13, GPVI and αIIbβ3 are sufficient to significantly inhibit washed platelet aggregation and decrease thrombus formation on fibrillar collagen. CONCLUSIONS. Our data demonstrate a role for MMP-13 in the inhibition of both platelet aggregation and thrombus formation in whole flowing blood, and may provide new avenues of research into the mechanisms underlying the subtle role of MMP-13 in atherothrombotic pathologies.

Item Type: Journal Article
Keywords: MMP13, Platelet
Faculty: Faculty of Science & Technology
Depositing User: Dr Nicholas Pugh
Date Deposited: 21 Feb 2018 16:48
Last Modified: 24 Apr 2019 11:05
URI: http://arro.anglia.ac.uk/id/eprint/702759

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