Tat-biliverdin reductase A inhibits inflammatory response by regulation of MAPK and NF-κB pathways in Raw 264.7 cells and edema mouse model

Mol Immunol. 2015 Feb;63(2):355-66. doi: 10.1016/j.molimm.2014.09.003. Epub 2014 Sep 17.

Abstract

Reactive oxygen species (ROS) accumulation induces oxidative stress and cell damage, which then activates several signaling pathways and triggers inflammatory response. Biliverdin is a natural product of heme metabolism which is converted to bilirubin by the enzyme biliverdin reductase A (BLVRA) which also plays a role in antioxidant activity via the ROS scavenging activity of bilirubin. In this study, we examined the anti-inflammatory and anti-apoptotic effects of Tat-BLVRA protein on lipopolysaccharide (LPS)-induced inflammation in Raw 264.7 macrophage cells. Transduction of Tat-BLVRA protein into Raw 264.7 cells and mice ear tissue was tested by Western blot analysis and immunohistochemical analysis. Tat-BLVRA protein was effective in inhibiting mitogen activated protein kinases (MAPKs), Akt and NF-κB activation, intracellular ROS production and DNA fragmentation. Also, Tat-BLVRA protein significantly inhibited the expression of cytokines, COX-2, and iNOS. In a 12-O-tetradecanoylphobol 13-acetate (TPA)-induced mouse model, mice ears treated with Tat-BLVRA protein showed decreased ear thickness and weight, as well as inhibited MAPKs activation and cytokine expression. Thus we suggested that Tat-BLVRA protein may provide an effective therapeutic agent for inflammatory skin diseases.

Keywords: Cytokine; Inflammation; MAPK; Protein therapy; ROS; Tat-BLVRA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Survival / drug effects
  • Disease Models, Animal
  • Edema / pathology
  • Edema / therapy*
  • Humans
  • Inflammation / enzymology
  • Inflammation / pathology*
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects
  • Macrophages / enzymology
  • Macrophages / pathology*
  • Male
  • Mice, Inbred ICR
  • Mitogen-Activated Protein Kinases / metabolism*
  • NF-kappa B / metabolism*
  • Oxidative Stress / drug effects
  • Oxidoreductases Acting on CH-CH Group Donors / genetics*
  • Oxidoreductases Acting on CH-CH Group Donors / therapeutic use*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Reactive Oxygen Species / metabolism
  • Recombinant Fusion Proteins / isolation & purification
  • Signal Transduction
  • Tetradecanoylphorbol Acetate
  • Transduction, Genetic
  • tat Gene Products, Human Immunodeficiency Virus / metabolism
  • tat Gene Products, Human Immunodeficiency Virus / therapeutic use*

Substances

  • Lipopolysaccharides
  • NF-kappa B
  • Reactive Oxygen Species
  • Recombinant Fusion Proteins
  • tat Gene Products, Human Immunodeficiency Virus
  • Oxidoreductases Acting on CH-CH Group Donors
  • biliverdin reductase
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases
  • Tetradecanoylphorbol Acetate