Ammonia drives dendritic cells into dysfunction

J Immunol. 2014 Aug 1;193(3):1080-9. doi: 10.4049/jimmunol.1303218. Epub 2014 Jun 25.

Abstract

Ammonia levels are often elevated in patients with cirrhosis or tumors. Patients with these diseases are immunocompromised. In this study, we investigated the effects of ammonia on a member of the immune cell family, the dendritic cells (DCs). Our results demonstrated that ammonia diminished cell count, phagocytosis, and lymphocyte stimulation of DCs. Ammonia also induced DC swelling, excessive reactive oxygen species production, and mitochondrial damage, which may constitute the underlying mechanism of ammonia-induced DC dysfunction. In ammonium chloride (NH4Cl)-loaded mice, DCs exhibited lowered phagocytosis and a weakened immune response to the chicken OVA vaccine. DCs from patients with cirrhosis or ammonia-treated healthy human blood both exhibited diminished phagocytosis. Moreover, tumor cell conditioned medium drove DCs into dysfunction, which could be reversed by ammonia elimination. In a murine colon carcinoma model, we found that ammonia could regulate tumor growth involving DCs and their related immune response. These findings reveal that ammonia could drive DCs into dysfunction, which contributes to the immunocompromised state of patients with cirrhosis or tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonium Chloride / toxicity*
  • Animals
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / pathology
  • Bone Marrow Cells / ultrastructure
  • Cell Count
  • Cell Line, Tumor
  • Coculture Techniques
  • Dendritic Cells / drug effects*
  • Dendritic Cells / pathology*
  • Dendritic Cells / ultrastructure
  • Humans
  • Liver Cirrhosis / immunology
  • Liver Cirrhosis / pathology
  • Lymphocyte Culture Test, Mixed / methods
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Middle Aged
  • Mitochondrial Membrane Transport Proteins / drug effects
  • Mitochondrial Membrane Transport Proteins / ultrastructure
  • Mitochondrial Permeability Transition Pore
  • Phagocytosis / drug effects
  • Phagocytosis / immunology
  • Primary Cell Culture

Substances

  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Permeability Transition Pore
  • Ammonium Chloride