Login / Signup

Effects of cigarette smoke extract on bronchial epithelial cells stimulated with Cryptococcus neoformans.

Aline Beatriz Mahler PereiraJhony Robison OliveiraAna Leticia Julio SouzaLeonardo Andrade-SilvaMarcos Vinicius SilvaPaulo Roberto SilvaMario Leon Silva-VergaraAlexandre de Paula Rogério
Published in: Medical microbiology and immunology (2021)
In the airways, the adhesion of Cryptococcus neoformans with airway epithelial cells is crucial for the establishment of cryptococcosis. Tobacco smoke is considered a risk factor for cryptococcosis. Here, we evaluated the effects of cigarette smoke extract (CSE) on human bronchial epithelial cells (BEAS-2B) stimulated with C. neoformans. Multiplicities of infection (MOIs) of 1-100 of C. neoformans per cell led to increased IL-8 production and no cytotoxic effects when compared to those of controls. C. neoformans (MOI 100) also significantly increased the concentration of IL-6. In cells stimulated with CSE doses (1.0, 2.5 and 5.0%) from one or five cigarettes, increased IL-1β production was observed only in doses from one (1.0%) and five (2.5%) cigarettes when compared to that of controls. However, only 1.0% CSE failed to show cytotoxic effects. In addition, CSE significantly increased the concentration of IL-8. Cells stimulated with both CSE and C. neoformans demonstrated a reduction in IL-6/STAT3 signalling compared to that in cells stimulated by C. neoformans. In addition, a significant increase in IL-10 production was also observed. No alterations in NF-kB or ICAM-1 expression were observed among the groups. The combination of CSE and C. neoformans favoured the increase of fungal numbers and extracellular adhering of C. neoformans on BEAS-2B cells. In addition, the internalization of C. neoformans on BEAS-2B cells was reduced after CSE stimulation. In conclusion, the association of CSE and C. neoformans induced an anti-inflammatory effect in bronchial epithelial cells, which might favour the development of C. neoformans infection in the airways.
Keyphrases
  • anti inflammatory
  • cell cycle arrest
  • signaling pathway
  • endothelial cells
  • stem cells
  • staphylococcus aureus
  • poor prognosis
  • cell proliferation
  • bone marrow
  • biofilm formation
  • lps induced