c-FLIP protects eosinophils from TNF-α-mediated cell death in vivo

PLoS One. 2014 Oct 21;9(10):e107724. doi: 10.1371/journal.pone.0107724. eCollection 2014.

Abstract

Understanding the signals that regulate eosinophil survival and death is critical to developing new treatments for asthma, atopy, and gastrointestinal disease. Previous studies suggest that TNF-α stimulation protects eosinophils from apoptosis, and this TNF-α-mediated protection is mediated by the upregulation of an unknown protein by NF-κB. Here, we show for the first time that eosinophils express the caspase 8-inhibitory protein c-FLIP, and c-FLIP expression is upregulated upon TNF-α stimulation. Considering that c-FLIP expression is regulated by NF-κB, we hypothesized that c-FLIP might serve as the "molecular switch" that converts TNFRI activation to a pro-survival signal in eosinophils. Indeed, we found that one c-FLIP isoform, c-FLIPL, is required for mouse eosinophil survival in the presence of TNF-α both in vitro and in vivo. Importantly, our results suggest c-FLIP as a potential therapeutic target for the treatment of eosinophil-mediated disease.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Bone Marrow Cells / cytology
  • Bone Marrow Transplantation
  • CASP8 and FADD-Like Apoptosis Regulating Protein / genetics
  • CASP8 and FADD-Like Apoptosis Regulating Protein / metabolism*
  • Cells, Cultured
  • Chromosomes, Artificial, Bacterial / genetics
  • Eosinophils / cytology
  • Eosinophils / drug effects
  • Eosinophils / metabolism*
  • Genotype
  • Mice
  • Mice, Transgenic
  • NF-kappa B / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Up-Regulation / drug effects

Substances

  • CASP8 and FADD-Like Apoptosis Regulating Protein
  • NF-kappa B
  • Tumor Necrosis Factor-alpha