MMP-9 coordinates multiple aspects of post-myocardial infarction left ventricular remodeling through direct molecular effects on extracellular matrix and inflammatory protein turnover.
This review highlights the critical role of MMP-9 in coordinating post-myocardial infarction left ventricular remodeling through extracellular matrix and inflammatory protein turnover.
Following myocardial infarction (MI), the left ventricle (LV) undergoes a series of cardiac wound healing responses that involve both the stimulation of robust inflammation to clear necrotic myocytes and tissue debris and the induction of extracellular matrix (ECM) protein synthesis to generate an infarct scar. The collective changes in myocardial structure and function are termed LV remodeling, and matrix metalloproteinase-9 (MMP-9) is a key instigator of post-MI LV remodeling. Through direct molecular effects on ECM and inflammatory protein turnover as well as indirect effects on major cell types that coordinate cardiac wound healing, namely the infiltrating leukocytes and the cardiac fibroblasts, MMP-9 coordinates multiple aspects of LV remodeling. In this review, we will discuss recent research that has expanded our understanding of post-MI LV remodeling, including recent proteomic advances focused on the ECM compartment to provide novel functional and translational insights. This overview will summarize how our understanding of MMP-9 has evolved over the last decade and will provide insight into future directions that will drive our understanding of MMP-9-directed cardiac ECM turnover in the post-MI LV.
Iyer et al. (Mon,) conducted a review in Myocardial infarction. MMP-9 signaling was evaluated. MMP-9 coordinates multiple aspects of post-myocardial infarction left ventricular remodeling through direct molecular effects on extracellular matrix and inflammatory protein turnover.