Combination of tumor necrosis factor-alpha ablation and matrix metalloproteinase inhibition prevents heart failure after pressure overload in tissue inhibitor of metalloproteinase-3 knock-out mice

Circ Res. 2005 Aug 19;97(4):380-90. doi: 10.1161/01.RES.0000178789.16929.cf. Epub 2005 Jul 21.

Abstract

Cytokine and extracellular matrix (ECM) homeostasis are distinct systems that are each dysregulated in heart failure. Here we show that tissue inhibitor of metalloproteinase (TIMP)-3 is a critical regulator of both systems in a mouse model of left ventricular (LV) dilation and dysfunction. Timp-3(-/-) mice develop precipitous LV dilation and dysfunction reminiscent of dilated cardiomyopathy (DCM), culminating in early onset of heart failure by 6 weeks, compared with wild-type aortic-banding (AB). Timp-3 deficiency resulted in increased TNFalpha converting enzyme (TACE) activity within 6 hours after AB leading to enhanced tumor necrosis factor-alpha (TNFalpha) processing. In addition, TNFalpha production increased in timp-3(-/-)-AB myocardium. A significant elevation in gelatinase and collagenase activities was observed 1 week after AB, with localized ECM degradation in timp-3(-/-)-AB myocardium. Timp-3(-/-)/tnfalpha(-/-) mice were generated and subjected to AB for comparative analyses with timp-3(-/-)-AB mice. This revealed the critical role of TNFalpha in the early phase of LV remodeling, de novo expression of Matrix metalloproteinases (MMP)-8 in the absence of TNFalpha, and highlighted the importance of interstitial collagenases (MMP-2, MMP-13, and MT1-MMP) for cardiac ECM degradation. Ablation of TNFalpha, or limiting MMP activity with a synthetic MMP inhibitor (PD166793), each partially attenuated LV dilation and cardiac dysfunction in timp-3(-/-)-AB mice. Notably, combining TNFalpha ablation with MMP inhibition completely rescued heart disease in timp-3(-/-)-AB mice. This study provides a basis for anti-TNFalpha and MMP inhibitor combination therapy in heart disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins
  • ADAM17 Protein
  • Animals
  • Apoptosis
  • Cardiomegaly / etiology
  • Heart Failure / etiology
  • Heart Failure / mortality
  • Heart Failure / prevention & control*
  • Matrix Metalloproteinase 8 / genetics
  • Matrix Metalloproteinase Inhibitors*
  • Matrix Metalloproteinases / physiology
  • Metalloendopeptidases / metabolism
  • Mice
  • Mice, Knockout
  • Protease Inhibitors / therapeutic use*
  • Tissue Inhibitor of Metalloproteinase-3 / physiology*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors*
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / physiology
  • Ventricular Dysfunction, Left / prevention & control

Substances

  • Matrix Metalloproteinase Inhibitors
  • Protease Inhibitors
  • Tissue Inhibitor of Metalloproteinase-3
  • Tumor Necrosis Factor-alpha
  • ADAM Proteins
  • Matrix Metalloproteinases
  • Metalloendopeptidases
  • Matrix Metalloproteinase 8
  • ADAM17 Protein
  • Adam17 protein, mouse