Candida albicans-induced acute lung injury through activating several inflammatory signaling pathways in mice

Int Immunopharmacol. 2019 Jul:72:275-283. doi: 10.1016/j.intimp.2019.04.026. Epub 2019 Apr 17.

Abstract

Candida albicans infection-induced acute lung injury is one of the most prevalent diseases in immunosuppressive individual. Nevertheless, the mechanism by which Candida albicans induced acute lung injury remains unclear. The present study investigated the mechanism by which Candida albicans induced acute lung injury in mice. Mice were randomly divided into four groups and intratracheally injected with 60 μl Candida albicans (106 CFU) or normal saline. Half of the mice were sacrificed at 6 h after Candida albicans. The rest of the mice for survival test were observed until 7 d after Candida albicans. As expected, immunosuppression aggravated Candida albicans-induced acute lung injury and death in mice. Additionally, Candida albicans infection elevated mRNA levels of pro-inflammatory and chemokines in lungs and the levels of IL-6, IL-1β and IL-17 in serum. Further study showed that Candida albicans promoted nuclear translocation of NF-κB p50 and p65 subunits in pulmonary epithelial cells and interstitial cells. Candida albicans induced pulmonary p38, ERK1/2 and Akt phosphorylation in normal and immunosuppressive mice. Moreover, Candida albicans infection activated pulmonary STAT3 signaling in normal and immunosuppressive mice. Overall, these results suggest that Candida albicans induced acute lung injury and death may be through activating several inflammatory signaling pathways.

Keywords: Acute lung injury; Candida albicans; Inflammatory signaling pathways; Mice.

MeSH terms

  • Acute Lung Injury / etiology
  • Acute Lung Injury / immunology*
  • Animals
  • Candida albicans
  • Candidiasis / complications
  • Candidiasis / immunology*
  • Cyclophosphamide
  • Cytokines / blood
  • Dexamethasone
  • Immunosuppression Therapy*
  • Inflammation / immunology
  • Lung / immunology
  • Male
  • Mice, Inbred BALB C
  • Mitogen-Activated Protein Kinases / immunology
  • NF-kappa B / immunology
  • Proto-Oncogene Proteins c-akt / immunology
  • STAT3 Transcription Factor / immunology
  • Signal Transduction

Substances

  • Cytokines
  • NF-kappa B
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Dexamethasone
  • Cyclophosphamide
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases