Matrix Metalloproteinase-9: Many Shades of Function in Cardiovascular Disease
Author(s) -
Andriy Yabluchanskiy,
Yonggang Ma,
Rugmani Padmanabhan Iyer,
Michael E. Hall,
Merry L. Lindsey
Publication year - 2013
Publication title -
physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.14
H-Index - 125
eISSN - 1548-9213
pISSN - 1548-9221
DOI - 10.1152/physiol.00029.2013
Subject(s) - matrix metalloproteinase , extracellular matrix , fibrosis , inflammation , disease , function (biology) , chemokine , pathological , microbiology and biotechnology , metalloproteinase , tissue inhibitor of metalloproteinase , medicine , biology , bioinformatics , immunology , pathology
Matrix metalloproteinase (MMP)-9, one of the most widely investigated MMPs, regulates pathological remodeling processes that involve inflammation and fibrosis in cardiovascular disease. MMP-9 directly degrades extracellular matrix (ECM) proteins and activates cytokines and chemokines to regulate tissue remodeling. MMP-9 deletion or inhibition has proven overall beneficial in multiple animal models of cardiovascular disease. As such, MMP-9 expression and activity is a common end point measured. MMP-9 cell-specific overexpression, however, has also proven beneficial and highlights the fact that little information is available on the underlying mechanisms of MMP-9 function. In this review, we summarize our current understanding of MMP-9 physiology, including structure, regulation, activation, and downstream effects of increased MMP-9. We discuss MMP-9 roles during inflammation and fibrosis in cardiovascular disease. By concentrating on the substrates of MMP-9 and their roles in cardiovascular disease, we explore the overall function and discuss future directions on the translational potential of MMP-9 based therapies.
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