Hirsutella sinensis mycelium suppresses interleukin-1β and interleukin-18 secretion by inhibiting both canonical and non-canonical inflammasomes

Sci Rep. 2013:3:1374. doi: 10.1038/srep01374.

Abstract

Cordyceps sinensis is a medicinal mushroom used for centuries in Asian countries as a health supplement and tonic. Hirsutella sinensis-the anamorphic, mycelial form of C. sinensis-possesses similar properties, and is increasingly used as a health supplement. Recently, C. sinensis extracts were shown to inhibit the production of the pro-inflammatory cytokine IL-1β in lipopolysaccharide-treated macrophages. However, the molecular mechanism underlying this process has remained unclear. In addition, whether H. sinensis mycelium (HSM) extracts also inhibit the production of IL-1β has not been investigated. In the present study, the HSM extract suppresses IL-1β and IL-18 secretion, and ATP-induced activation of caspase-1. Notably, we observed that HSM not only reduced expression of the inflammasome component NLRP1 and the P2X7R but also reduced the activation of caspase-4, and ATP-induced ROS production. These findings reveal that the HSM extract has anti-inflammatory properties attributed to its ability to inhibit both canonical and non-canonical inflammasomes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Adenosine Triphosphate / pharmacology
  • Apoptosis Regulatory Proteins / metabolism
  • Ascomycota / metabolism*
  • Caspases / metabolism
  • Down-Regulation / drug effects
  • Enzyme Activation / drug effects
  • Ethanol
  • Humans
  • Inflammasomes / antagonists & inhibitors*
  • Inflammasomes / metabolism
  • Interleukin-18 / genetics
  • Interleukin-18 / metabolism*
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism*
  • Lipopolysaccharides / pharmacology
  • Macrophage Activation / drug effects
  • Macrophages / drug effects
  • Macrophages / enzymology
  • Macrophages / metabolism
  • Macrophages / microbiology
  • Models, Biological
  • Mycelium / metabolism*
  • NLR Proteins
  • Reactive Oxygen Species / metabolism
  • Receptors, Purinergic P2X4 / metabolism
  • Receptors, Purinergic P2X7 / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Apoptosis Regulatory Proteins
  • Inflammasomes
  • Interleukin-18
  • Interleukin-1beta
  • Lipopolysaccharides
  • NLR Proteins
  • NLRP1 protein, human
  • Reactive Oxygen Species
  • Receptors, Purinergic P2X4
  • Receptors, Purinergic P2X7
  • Ethanol
  • Adenosine Triphosphate
  • Caspases