Multiple ASC-dependent inflammasomes drive differential pro-inflammatory cytokine production in a mouse model of tendinopathy

Biosci Rep. 2024 Nov 27;44(11):BSR20241282. doi: 10.1042/BSR20241282.

Abstract

Inflammasomes are multiprotein complexes that regulate the bioactive production of IL-1β and IL-18, being implicated in the inflammatory response of different diseases. The inflammasome formed by the cytosolic sensor NLRP3 is highly promiscuous, as it could be activated by different pathogen- and sterile-signals. However, few models have studied the implication of NLRP3 in tissue damage-induced inflammation, particularly the implication of NLRP3 in tendinopathies. Here, we aimed to investigate the implication of NLRP3 in a mouse model of tendinopathy by collagenase degradation of the extracellular matrix in the Achilles' mice tendon. We found that NLRP3 was involved in the production of IL-1β, but another ASC-dependent inflammasome was required to produce IL-18 during sterile tissue damage. Our study suggests that in the immune response to extracellular matrix degradation different inflammasomes, probably expressed in different cell compartments, were able to differentially control IL-1β and IL-18 production in vivo. These results suggest the potential use of therapies targeting ASC as beneficial in the treatment of tendinopathies.

Keywords: ASC; Collagenase; NLRP3; inflammasome; sterile tissue damage; tendon.

MeSH terms

  • Achilles Tendon / immunology
  • Achilles Tendon / metabolism
  • Achilles Tendon / pathology
  • Animals
  • CARD Signaling Adaptor Proteins* / genetics
  • CARD Signaling Adaptor Proteins* / metabolism
  • Disease Models, Animal*
  • Extracellular Matrix / immunology
  • Extracellular Matrix / metabolism
  • Inflammasomes* / immunology
  • Inflammasomes* / metabolism
  • Interleukin-18* / genetics
  • Interleukin-18* / metabolism
  • Interleukin-1beta* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism
  • Tendinopathy* / immunology
  • Tendinopathy* / metabolism
  • Tendinopathy* / pathology

Substances

  • Inflammasomes
  • Interleukin-18
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Interleukin-1beta
  • Nlrp3 protein, mouse
  • CARD Signaling Adaptor Proteins
  • IL1B protein, mouse
  • Pycard protein, mouse