Left ventricular remodeling in transgenic mice with cardiac restricted overexpression of tumor necrosis factor

Natarajan Sivasubramanian, Mytsi L. Coker, Karla M. Kurrelmeyer, William R. MacLellan, Francesco J. DeMayo, Francis G. Spinale, Douglas L. Mann

Research output: Contribution to journalArticle

291 Scopus citations

Abstract

Background - The mechanisms responsible for tumor necrosis factor (TNF) - induced LV structural remodeling in the adult heart are not known. Methods and Results - We generated a line of transgenic mice (MHCsTNF) with cardiac restricted overexpression of TNF that develop progressive LV dilation/remodeling from 4 to 12 weeks of age. During the early phases of LV structural remodeling, there was a significant increase in total matrix metalloproteinase (MMP) activity that corresponded to a decrease in total myocardial fibrillar collagen content. As the MHCsTNF mice aged, there was a significant decrease in total MMP zymographic activity that was accompanied by an increase in total fibrillar collagen content. The changes in total MMP activity and myocardial fibrillar collagen content were related to a time- dependent increase in myocardial tissue inhibitor of metalloproteinases (TIMP)-1 levels, resulting in a significant time-dependent decrease in the MMP activity/TIMP level ratio in the MHCsTNF mice. To determine a possible mechanism for the increase in myocardial fibrosis, we also measured levels of TGF-β1 and TGF-β2 protein levels, which were shown to be significantly elevated in the hearts of the MHCsTNF mice. Conclusions - Our results suggest that progressive time-dependent changes in the balance between MMP activity and TIMP activity are responsible, at least in part, for the spectrum of TNF-induced changes in the myofibrillar collagen content that occur during LV structural remodeling in the MHCsTNF mice.

Original languageEnglish (US)
Pages (from-to)826-831
Number of pages6
JournalCirculation
Volume104
Issue number7
DOIs
StatePublished - Aug 14 2001

Keywords

  • Collagen
  • Genes
  • Growth substances
  • Heart failure
  • Tumor necrosis factor

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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