PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway

Respir Res. 2018 Mar 2;19(1):37. doi: 10.1186/s12931-017-0702-y.

Abstract

Background: The contribution of airway remodeling in chronic obstructive pulmonary disease (COPD) has been well documented, with airway smooth muscle cell proliferation and migration playing a role in the remodeling process. Here, we aimed to verify the effects of fine particulate matter (PM2.5) on human bronchial smooth muscle cell (HBSMC) migration and to explore the underlying signaling pathways.

Methods: HBSMC apoptosis, proliferation and migration were measured using flow cytometry, cell counting and transwell migration assays, respectively. The role of the hedgehog pathway in cell migration was assessed by western blotting to measure the expression of Sonic hedgehog (Shh), Gli1 and Snail. Furthermore, siRNA was used to knock down Gli1 or Snail expression.

Results: PM2.5 induced HBSMC apoptosis in a dose-dependent manner, although certain concentrations of PM2.5 did not induce HBSMC proliferation or apoptosis. Interestingly, cell migration was stimulated by PM2.5 doses far below those that induced apoptosis. Additional experiments revealed that these PM2.5 doses enhanced the expression of Shh, Gli1 and Snail in HBSMCs. Furthermore, PM2.5-induced cell migration and protein expression were enhanced by recombinant Shh and attenuated by cyclopamine. Similar results were obtained by knocking down Gli1 or Snail.

Conclusions: These findings suggest that PM2.5, which may exert its effects through the Shh signaling pathway, is necessary for the migration of HBSMCs. These data define a novel role for PM2.5 in airway remodeling in COPD.

Keywords: COPD; Human bronchial smooth muscle cell; Migration; PM2.5; Sonic hedgehog signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bronchi / drug effects
  • Bronchi / metabolism*
  • Bronchi / pathology
  • Cell Movement / drug effects
  • Cell Movement / physiology*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Hedgehog Proteins / metabolism*
  • Humans
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism*
  • Particulate Matter / toxicity*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*

Substances

  • Hedgehog Proteins
  • Particulate Matter