Science and Research

Haemophilus influenzae causes cellular trans-differentiation in human bronchial epithelia

Non-typeable Haemophilus influenzae (NTHi) is the most common respiratory pathogen in patients with chronic obstructive disease. Limited data is available investigating the impact of NTHi infections on cellular re-differentiation processes in the bronchial mucosa. The aim of this study was to assess the effects of stimulation with NTHi on the bronchial epithelium regarding cellular re-differentiation processes using primary bronchial epithelial cells harvested from infection-free patients undergoing bronchoscopy. The cells were then cultivated using an air-liquid interface and stimulated with NTHi and TGF-β. Markers of epithelial and mesenchymal cells were analyzed using immunofluorescence, Western blot and qRT-PCR. Stimulation with both NTHi and TGF-ß led to a marked increase in the expression of the mesenchymal marker vimentin, while E-cadherin as an epithelial marker maintained a stable expression throughout the experiments. Furthermore, expression of collagen 4 and the matrix-metallopeptidases 2 and 9 were increased after stimulation, while the expression of tissue inhibitors of metallopeptidases was not affected by pathogen stimulation. In this study we show a direct pathogen-induced trans-differentiation of primary bronchial epithelial cells resulting in a co-localization of epithelial and mesenchymal markers and an up-regulation of extracellular matrix components.

  • Glöckner, M.
  • Marwitz, S.
  • Rohmann, K.
  • Watz, H.
  • Nitschkowski, D.
  • Rupp, J.
  • Dalhoff, K.
  • Goldmann, T.
  • Drömann, D.

Keywords

  • Chronic obstructive pulmonary disease
  • epithelial-mesenchymal transition
  • non-typeable Haemophilus influenzae
  • primary bronchial epithelial cells
Publication details
DOI: 10.1177/1753425921994906
Journal: Innate Immun
Pages: 1753425921994906 
Work Type: Original
Location: Assoziierter Partner, ARCN
Disease Area: COPD
Partner / Member: FZB, PRI, UKSH (Lübeck)
Access-Number: 33646896

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