A Selective Matrix Metalloproteinase-12 Inhibitor Retards Atherosclerotic Plaque Development in Apolipoprotein E–Knockout Mice
Author(s) -
Jason L. Johnson,
Laurent Devel,
Bertrand Czarny,
Sarah J. George,
Christopher L. Jackson,
Vassilis Rogakos,
Fabrice Beau,
Athanasios Yiotakis,
Andrew C. Newby,
Vincent Dive
Publication year - 2011
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.110.219147
Subject(s) - fibrous cap , knockout mouse , apolipoprotein e , matrix metalloproteinase , macrophage , apolipoprotein b , apoptosis , in vivo , foam cell , vulnerable plaque , endocrinology , cancer research , biology , medicine , chemistry , in vitro , biochemistry , receptor , cholesterol , microbiology and biotechnology , disease
Matrix metalloproteinase (MMP)-12 has been implicated in plaque progression and instability and is also amenable to selective inhibition. In this study, we investigated the influence of a greater than 10-fold selective synthetic MMP-12 inhibitor on plaque progression in the apolipoprotein E knockout mouse model of atherosclerosis.
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