Cellular FLIP is expressed in cardiomyocytes and down-regulated in TUNEL-positive grafted cardiac tissues

Cardiovasc Res. 2000 Oct;48(1):101-10. doi: 10.1016/s0008-6363(00)00154-1.

Abstract

Objective: c-FLIP is a natural homologue of caspase 8, and may antagonize activation of death pathways mediated by FADD. c-FLIP is highly expressed in the heart, and a recent report suggests that c-FLIP may protect against certain types of myocyte death. The present study was designed to define the expression patterns of c-FLIP in the heart.

Methods: The expression pattern of c-FLIP in end-stage human hearts, and rat cardiomyocyte grafting models was analyzed by in situ hybridization, immunohistochemistry and TUNEL assay. In addition, to determine whether Fas-dependent pathway is active in cardiomyocytes in vitro, we examined whether activated monocytes can kill neonatal cardiomyocytes in a co-culture system.

Results: c-FLIP mRNA and protein were abundantly expressed in normal cardiomyocytes from failing human heart. In animal models, c-FLIP protein was absent in TUNEL-positive grafted cardiomyocytes. Double staining demonstrated that c-FLIP-positive cells rarely had fragmented DNA, while TUNEL-positive cells rarely contained c-FLIP. Finally, activated monocytes induced death of neonatal rat cardiomyocytes via the Fas/FasL system.

Conclusions: Loss of c-FLIP expression correlates with cardiomyocyte cell death. We hypothesize that diminished c-FLIP expression may predispose cardiomyocytes to apoptotic death.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Animals
  • Animals, Newborn
  • Apoptosis
  • Blotting, Western
  • Caspases / metabolism*
  • Cell Transplantation
  • Coculture Techniques
  • DNA Fragmentation
  • Dogs
  • Enzyme Inhibitors / metabolism
  • Fas Ligand Protein
  • Female
  • Gene Expression
  • Heart Failure / metabolism*
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • In Situ Nick-End Labeling
  • Leukocytes, Mononuclear
  • Lymphocyte Activation
  • Male
  • Membrane Glycoproteins / metabolism
  • Middle Aged
  • Models, Animal
  • Myocardium / metabolism*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Inbred F344
  • fas Receptor / metabolism

Substances

  • Enzyme Inhibitors
  • FASLG protein, human
  • Fas Ligand Protein
  • Faslg protein, rat
  • Membrane Glycoproteins
  • RNA, Messenger
  • fas Receptor
  • Caspases