Inhibition of neddylation regulates dendritic cell functions via Deptor accumulation driven mTOR inactivation

Oncotarget. 2016 Jun 14;7(24):35643-35654. doi: 10.18632/oncotarget.9543.

Abstract

Neddylation, a newly identified post-translational modification, is significant for the activity and stability of target proteins. The exact role of neddylation in the pathogenesis of inflammatory bowel disease, specifically those mediated by dendritic cells (DCs), was still rarely reported. Here, we showed that inhibition of neddylation protected mice from mucosal inflammation. Targeting neddylation also inhibited DC maturation characterized by reduced cytokine production, down-regulated costimulatory molecules and suppressed capacity in allogeneic T cell stimulation. Additionally, inactivation of neddylation promotes caspase dependent apoptosis of DCs. These phenomena were attributed to the inactivation of mTOR, which was caused by Cullin-1 deneddylation induced Deptor accumulation. Together, our findings revealed that neddylation inhibition suppressed DC functions through mTOR signaling pathway and provided a potential therapeutic opportunity in inflammatory bowel diseases.

Keywords: Deptor; Immune response; Immunity; Immunology and Microbiology Section; dendritic cell; inflammatory bowel disease; mTOR; neddylation.

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Caspase 3 / metabolism
  • Caspase 7 / metabolism
  • Cell Differentiation
  • Cells, Cultured
  • Cullin Proteins / metabolism*
  • Cyclopentanes / pharmacology
  • Cyclopentanes / therapeutic use
  • Cytokines / metabolism
  • Dendritic Cells / physiology*
  • Disease Models, Animal
  • Down-Regulation
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use
  • Humans
  • Inflammatory Bowel Diseases / drug therapy
  • Inflammatory Bowel Diseases / immunology*
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Protein Processing, Post-Translational / drug effects
  • Protein Processing, Post-Translational / physiology*
  • Pyrimidines / pharmacology
  • Pyrimidines / therapeutic use
  • Signal Transduction / drug effects
  • TOR Serine-Threonine Kinases / metabolism*

Substances

  • Cullin 1
  • Cullin Proteins
  • Cyclopentanes
  • Cytokines
  • Enzyme Inhibitors
  • Intracellular Signaling Peptides and Proteins
  • Pyrimidines
  • deptor protein, mouse
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • Casp3 protein, mouse
  • Casp7 protein, mouse
  • Caspase 3
  • Caspase 7
  • pevonedistat