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pyroptosis
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pyroptosis

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Also known as GO:0070269

Pyroptosis is a highly inflammatory form of lytic programmed cell death that occurs most frequently upon infection with intracellular pathogens and forms part of the antimicrobial response. This process promotes the rapid clearance of various bacterial, viral, fungal and protozoan infections by removing intracellular replication niches and enhancing the host's defensive responses. Pyroptosis can take place in immune cells and is also reporte d to occur in keratinocytes and some epithelial cells.

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Article

14 sections
Contents
  • Discovery
  • Morphological characteristics
  • Mechanism
  • The canonical inflammasome pathway
  • The noncanonical inflammasome pathway
  • Caspase-3-dependent cell death pathway
  • Clinical relevance
  • Infection
  • Cerebrovascular disease
  • Cancer
  • Metabolic disorder
  • Cryopyrinopathies
  • HIV and AIDS
  • References

Pyroptosis is a highly inflammatory form of lytic programmed cell death that occurs most frequently upon infection with intracellular pathogens and forms part of the antimicrobial response. This process promotes the rapid clearance of various bacterial, viral, fungal and protozoan infections by removing intracellular replication niches and enhancing the host's defensive responses. Pyroptosis can take place in immune cells and is also reporte d to occur in keratinocytes and some epithelial cells.

The process is initiated by formation of a large supramolecular complex termed the inflammasome (also known as a pyroptosome) upon intracellular danger signals. The inflammasome activates a different set of caspases as compared to apoptosis, for example, caspase-1/4/5 in humans and caspase-11 in mice. These caspases contribute to the maturation and activation of the pro-inflammatory cytokines IL-1β and IL-18, as well as the pore-forming protein gasdermin D. Formation of pores causes cell membrane rupture and release of cytokines, as well as various damage-associated molecular pattern (DAMP) molecules such as HMGB-1, ATP and DNA, out of the cell. These molecules recruit more immune cells and further perpetuate the inflammatory cascade in the tissue.

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