Double-stranded RNA induces chicken T-cell lymphoma apoptosis by TRIF and NF-κB

Sci Rep. 2017 Aug 8;7(1):7547. doi: 10.1038/s41598-017-07919-w.

Abstract

Toll-like receptor-3 (TLR3), a member of the pathogen recognition receptor family, has been reported to activate immune response and to exhibit pro-apoptotic activity against some tumor cells. However it is unclear whether TLR3 has same function against chicken lymphoma. In this paper we investigated the effect of TLR3 activation on a Marek's disease lymphoma-derived chicken cell line, MDCC-MSB1. The TLR3 agonist poly (I:C) activated TLR3 pathway and inhibited tumor cells proliferation through caspase-dependent apoptosis. Using pharmacological approaches, we found that an interferon-independent mechanism involving Toll-IL-1-receptor domain-containing adapter-inducing IFN-α (TRIF) and nuclear factor κB (NF-κB) causes the apoptosis of MDCC-MSB1 cells. This is the first report about the function of TLR3 in chicken T-cell lymphoma, especially in signal pathway. The mechanisms underlying TLR3-mediated apoptosis may contribute to the development of new drug to treat lymphomas and oncovirus infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics*
  • Adaptor Proteins, Vesicular Transport / metabolism
  • Animals
  • Apoptosis / drug effects
  • Apoptosis / genetics*
  • Avian Proteins / genetics
  • Avian Proteins / metabolism
  • Cell Line, Tumor
  • Chickens
  • Lymphoma, T-Cell / genetics
  • Lymphoma, T-Cell / metabolism
  • Lymphoma, T-Cell / pathology
  • NF-kappa B / genetics*
  • NF-kappa B / metabolism
  • Poly I-C / pharmacology
  • RNA, Double-Stranded / genetics*
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Toll-Like Receptor 3 / agonists
  • Toll-Like Receptor 3 / metabolism

Substances

  • Adaptor Proteins, Vesicular Transport
  • Avian Proteins
  • NF-kappa B
  • RNA, Double-Stranded
  • Toll-Like Receptor 3
  • Poly I-C