TNF dually mediates resistance and susceptibility to mycobacteria via mitochondrial reactive oxygen species

Cell. 2013 Apr 25;153(3):521-34. doi: 10.1016/j.cell.2013.03.022. Epub 2013 Apr 11.

Abstract

Tumor necrosis factor (TNF) constitutes a critical host defense against tuberculosis, but its excess is also implicated in tuberculosis pathogenesis in zebrafish and humans. Using the zebrafish, we elucidate the pathways by which TNF mediates tuberculosis pathogenesis. TNF excess induces mitochondrial reactive oxygen species (ROS) in infected macrophages through RIP1-RIP3-dependent pathways. While initially increasing macrophage microbicidal activity, ROS rapidly induce programmed necrosis (necroptosis) and release mycobacteria into the growth-permissive extracellular milieu. TNF-induced necroptosis occurs through two pathways: modulation of mitochondrial cyclophilin D, implicated in mitochondrial permeability transition pore formation, and acid sphingomyelinase-mediated ceramide production. Combined genetic blockade of cyclophilin D and acid sphingomyelinase renders the high TNF state hyperresistant by preventing macrophage necrosis while preserving increased microbicidal activity. Similarly, the cyclophilin D-inhibiting drug alisporivir and the acid sphingomyelinase-inactivating drug, desipramine, synergize to reverse susceptibility, suggesting the therapeutic potential of these orally active drugs against tuberculosis and possibly other TNF-mediated diseases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cyclophilin D
  • Cyclophilins / metabolism
  • Disease Models, Animal
  • Disease Susceptibility
  • Humans
  • Macrophages / immunology
  • Metabolic Networks and Pathways
  • Mitochondria / metabolism*
  • Mycobacterium / physiology*
  • Necrosis*
  • Reactive Oxygen Species / metabolism*
  • Receptor-Interacting Protein Serine-Threonine Kinases / metabolism
  • Tuberculosis / drug therapy
  • Tuberculosis / genetics*
  • Tuberculosis / immunology
  • Tumor Necrosis Factors / genetics*
  • Tumor Necrosis Factors / immunology
  • Tumor Necrosis Factors / metabolism
  • Zebrafish

Substances

  • Cyclophilin D
  • Reactive Oxygen Species
  • Tumor Necrosis Factors
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Cyclophilins