Caspase-1 in Cx3cr1-expressing cells drives an IL-18-dependent T cell response that promotes parasite control during acute Toxoplasma gondii infection

PLoS Pathog. 2024 Oct 24;20(10):e1012006. doi: 10.1371/journal.ppat.1012006. eCollection 2024 Oct.

Abstract

Inflammasome activation is a robust innate immune mechanism that promotes inflammatory responses through the release of alarmins and leaderless cytokines, including IL-1α, IL-1β, and IL-18. Various stimuli, including infectious agents and cellular stress, cause inflammasomes to assemble and activate caspase-1. Then, caspase-1 cleaves targets that lead to pore formation and leaderless cytokine activation and release. Toxoplasma gondii has been shown to promote inflammasome formation, but the cell types utilizing caspase-1 and the downstream effects on immunological outcomes during acute in vivo infection have not been explored. Here, using knockout mice, we examine the role of caspase-1 responses during acute T. gondii infection globally and in Cx3cr1-positive populations. We provide in vivo evidence that caspase-1 expression is critical for, IL-18 release, optimal interferon-γ (IFN-γ) production, monocyte and neutrophil recruitment to the site of infection, and parasite control. Specifically, we find that caspase-1 expression in Cx3cr1-positive cells drives IL-18 release, which potentiates CD4+ T cell IFN-γ production and parasite control. Notably, our Cx3cr1-Casp1 knockouts exhibited a selective T cell defect, mirroring the phenotype observed in Il18 knockouts. In further support of this finding, treatment of Cx3cr1-Casp1 knockout mice with recombinant IL-18 restored CD4+ T cell IFN-γ responses and parasite control. Additionally, we show that neutrophil recruitment is dependent on IL-1 receptor accessory protein (IL-1RAP) signaling but is dispensable for parasite control. Overall, these experiments highlight the multifaceted role of caspase-1 in multiple cell populations contributing to specific pathways that collectively contribute to caspase-1 dependent immunity to T. gondii.

MeSH terms

  • Animals
  • CX3C Chemokine Receptor 1* / genetics
  • CX3C Chemokine Receptor 1* / metabolism
  • Caspase 1* / metabolism
  • Inflammasomes / immunology
  • Inflammasomes / metabolism
  • Interleukin-18* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • Toxoplasma* / immunology
  • Toxoplasmosis* / immunology
  • Toxoplasmosis* / metabolism
  • Toxoplasmosis* / parasitology
  • Toxoplasmosis, Animal / immunology
  • Toxoplasmosis, Animal / parasitology

Substances

  • Interleukin-18
  • Caspase 1
  • CX3C Chemokine Receptor 1
  • Cx3cr1 protein, mouse
  • Casp1 protein, mouse
  • Inflammasomes