TNF-α modulates TLR2-dependent responses during mycobacterial infection

Methods Mol Biol. 2014:1155:133-50. doi: 10.1007/978-1-4939-0669-7_12.

Abstract

Multifunctional roles of tumor necrosis factor-alpha (TNF-α) during the mycobacterial pathogenesis make it an important molecule to understand and to examine the course of infection. Identification and analysis of TNF-α response can largely contribute to determine the potential host mediators for therapeutic intervention against tuberculosis. The current chapter describes several methods to assess the ability of TNF-α signaling to modulate toll-like receptor (TLR)2 signaling, another key player in mycobacterial infection and its responses. Experiments involving neutralizing antibodies, antagonists, pharmacological inhibitors, and siRNA-mediated gene silencing are discussed in this chapter to establish the role of TNF-α signaling. The widely used protein and mRNA analysis readouts like enzyme-linked immunosorbent assay (ELISA), immunoblotting, fluorescence-activated cell sorting (FACS), and quantitative real-time RT-PCR are useful to estimate and confirm the mediators involved in TNF-α and TLR2 signaling.

MeSH terms

  • Animals
  • Apoptosis
  • Blotting, Western
  • Cells, Cultured
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Humans
  • Lipopolysaccharides / pharmacology
  • Macrophages, Peritoneal / cytology*
  • Macrophages, Peritoneal / metabolism
  • Macrophages, Peritoneal / microbiology
  • Mice
  • Mice, Inbred C57BL
  • Mycobacterium / pathogenicity*
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Toll-Like Receptor 2 / metabolism*
  • Tuberculosis / immunology*
  • Tuberculosis / physiopathology
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Lipopolysaccharides
  • NF-kappa B
  • RNA, Messenger
  • Toll-Like Receptor 2
  • Tumor Necrosis Factor-alpha