A biphasic innate immune MAPK response discriminates between the yeast and hyphal forms of Candida albicans in epithelial cells

Cell Host Microbe. 2010 Sep 16;8(3):225-35. doi: 10.1016/j.chom.2010.08.002.

Abstract

Discriminating between commensal and pathogenic states of opportunistic pathogens is critical for host mucosal defense and homeostasis. The opportunistic human fungal pathogen Candida albicans is also a constituent of the normal oral flora and grows either as yeasts or hyphae. We demonstrate that oral epithelial cells orchestrate an innate response to C. albicans via NF-κB and a biphasic MAPK response. Activation of NF-κB and the first MAPK phase, constituting c-Jun activation, is independent of morphology and due to fungal cell wall recognition. Activation of the second MAPK phase, constituting MKP1 and c-Fos activation, is dependent upon hypha formation and fungal burdens and correlates with proinflammatory responses. Such biphasic response may allow epithelial tissues to remain quiescent under low fungal burdens while responding specifically and strongly to damage-inducing hyphae when burdens increase. MAPK/MKP1/c-Fos activation may represent a "danger response" pathway that is critical for identifying and responding to the pathogenic switch of commensal microbes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Candida albicans / cytology
  • Candida albicans / growth & development
  • Candida albicans / immunology*
  • Candida albicans / pathogenicity*
  • Candidiasis, Oral / immunology
  • Cell Line, Tumor
  • Cell Wall / immunology
  • Cytokines / metabolism
  • Dual Specificity Phosphatase 1 / metabolism
  • Epithelial Cells / immunology*
  • Epithelial Cells / metabolism
  • Epithelial Cells / microbiology*
  • Fungal Proteins / metabolism
  • Host-Pathogen Interactions
  • Humans
  • Hyphae / immunology
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinases / metabolism*
  • Mouth Mucosa / immunology*
  • Mouth Mucosa / metabolism
  • Mouth Mucosa / microbiology*
  • NF-kappa B / metabolism
  • Proto-Oncogene Proteins c-fos / metabolism
  • Signal Transduction
  • Virulence
  • Yeasts / metabolism

Substances

  • Cytokines
  • Fungal Proteins
  • NF-kappa B
  • Proto-Oncogene Proteins c-fos
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinases
  • Dual Specificity Phosphatase 1