Matrix metalloproteinase-28 deletion exacerbates cardiac dysfunction and rupture after myocardial infarction in mice by inhibiting M2 macrophage activation

Circ Res. 2013 Feb 15;112(4):675-88. doi: 10.1161/CIRCRESAHA.111.300502. Epub 2012 Dec 20.

Abstract

Rationale: Matrix metalloproteinase (MMP)-28 regulates the inflammatory and extracellular matrix responses in cardiac aging, but the roles of MMP-28 after myocardial infarction (MI) have not been explored.

Objective: To determine the impact of MMP-28 deletion on post-MI remodeling of the left ventricle (LV).

Methods and results: Adult C57BL/6J wild-type (n=76) and MMP null (MMP-28((-/-)), n=86) mice of both sexes were subjected to permanent coronary artery ligation to create MI. MMP-28 expression decreased post-MI, and its cell source shifted from myocytes to macrophages. MMP-28 deletion increased day 7 mortality because of increased cardiac rupture post-MI. MMP-28(-/-) mice exhibited larger LV volumes, worse LV dysfunction, a worse LV remodeling index, and increased lung edema. Plasma MMP-9 levels were unchanged in the MMP-28((-/-)) mice but increased in wild-type mice at day 7 post-MI. The mRNA levels of inflammatory and extracellular matrix proteins were attenuated in the infarct regions of MMP-28(-/-) mice, indicating reduced inflammatory and extracellular matrix responses. M2 macrophage activation was impaired when MMP-28 was absent. MMP-28 deletion also led to decreased collagen deposition and fewer myofibroblasts. Collagen cross-linking was impaired as a result of decreased expression and activation of lysyl oxidase in the infarcts of MMP-28(-/-) mice. The LV tensile strength at day 3 post-MI, however, was similar between the 2 genotypes.

Conclusions: MMP-28 deletion aggravated MI-induced LV dysfunction and rupture as a result of defective inflammatory response and scar formation by suppressing M2 macrophage activation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Adhesion Molecules / biosynthesis
  • Cell Adhesion Molecules / genetics
  • Cicatrix / enzymology
  • Cicatrix / etiology
  • Collagen / metabolism
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Extracellular Matrix Proteins / biosynthesis
  • Extracellular Matrix Proteins / genetics
  • Female
  • Gene Expression Regulation
  • Heart Rupture / enzymology*
  • Heart Rupture / etiology
  • Inflammation
  • Macrophage Activation / physiology*
  • Macrophages / classification
  • Macrophages / enzymology
  • Male
  • Matrix Metalloproteinase 9 / blood
  • Matrix Metalloproteinases, Secreted / deficiency*
  • Matrix Metalloproteinases, Secreted / genetics
  • Matrix Metalloproteinases, Secreted / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myocardial Infarction / blood
  • Myocardial Infarction / complications
  • Myocardial Infarction / enzymology*
  • Myocardial Infarction / physiopathology
  • Myocytes, Cardiac / enzymology
  • Myofibroblasts / metabolism
  • Protein-Lysine 6-Oxidase / metabolism
  • Pulmonary Edema / enzymology
  • Pulmonary Edema / etiology
  • Receptors, Cytokine / biosynthesis
  • Receptors, Cytokine / genetics
  • Transcription, Genetic
  • Ventricular Dysfunction, Left / enzymology*
  • Ventricular Dysfunction, Left / etiology
  • Ventricular Remodeling / genetics
  • Ventricular Remodeling / physiology

Substances

  • Cell Adhesion Molecules
  • Cytokines
  • Extracellular Matrix Proteins
  • Receptors, Cytokine
  • Collagen
  • Protein-Lysine 6-Oxidase
  • Matrix Metalloproteinases, Secreted
  • Mmp28 protein, mouse
  • Matrix Metalloproteinase 9