Levels of Circulating MMCN-151, a Degradation Product of Mimecan, Reflect Pathological Extracellular Matrix Remodeling in Apolipoprotein E Knockout Mice
Author(s) -
Natasha Barascuk,
Efstathios Vassiliadis,
Q. Zheng,
Yong Wang,
W. Wang,
Lise Larsen,
Lars Melholt Rasmussen,
M.A. Karsdal
Publication year - 2011
Publication title -
biomarker insights
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.075
H-Index - 31
ISSN - 1177-2719
DOI - 10.4137/bmi.s7777
Subject(s) - apolipoprotein e , extracellular matrix , knockout mouse , matrix metalloproteinase , medicine , apolipoprotein b , endocrinology , disease , biology , microbiology and biotechnology , receptor , cholesterol
Arterial extracellular matrix (ECM) remodeling by matrix metalloproteinases (MMPs) is one of the major hallmarks of atherosclerosis. Mimecan, also known as osteoglycin has been implicated in the integrity of the ECM. This study assessed the validity of an enzyme-linked immunosorbent assay (ELISA) developed to measure a specific MMP12-derived fragment of mimecan, MMCN-151, in apolipoprotein-E knockout (ApoE-KO) mice.
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