Airborne particulate matter impairs corneal epithelial cells migration via disturbing FAK/RhoA signaling pathway and cytoskeleton organization

Nanotoxicology. 2018 May;12(4):312-324. doi: 10.1080/17435390.2018.1440651. Epub 2018 Feb 20.

Abstract

Background: Cornea is the outmost structure of the eye and exposed directly to the air pollution. However, little is known about the effect of PM2.5 on corneal epithelium, which is critical for maintenance of cornea homeostasis and visual function.

Objective: We investigated the influence of PM2.5 exposure on corneal epithelial migration and the possible mechanisms involved in the process.

Methods: We observed wound healing in mouse model of cornea abrasion, evaluated the migration and mobility of cultured corneal epithelial cells with wound scratch assay and Transwell migration assay, detected the phosphorylation and interaction of FAK/paxillin with immunofluorescence and immunoprecipitation, and determined the RhoA activity and actin reorganization, in response to PM2.5 exposure.

Results: Exposure to PM2.5 remarkably inhibited corneal epithelial cell migration both in mouse model of corneal abrasion and in cell culture model. We found the phosphorylation and interaction of FAK/paxillin, RhoA activity as well as actin reorganization were suppressed by PM2.5 exposure. Moreover, formation of ROS might play a role in the action of PM2.5.

Conclusions: PM2.5 exposure could result in delay of corneal epithelium wound healing by inhibiting cell migration, thus more attention should be paid to the potential risk of corneal infection and effort should be made to protect eyes against impairment induced by PM2.5.

Keywords: PM2.5; cornea; epithelium; migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Cell Movement / drug effects*
  • Cytoskeleton / drug effects*
  • Epithelial Cells / drug effects
  • Epithelium, Corneal / cytology
  • Epithelium, Corneal / drug effects*
  • Epithelium, Corneal / enzymology
  • Epithelium, Corneal / metabolism*
  • Focal Adhesion Kinase 1 / metabolism*
  • Humans
  • Mice
  • Particulate Matter / toxicity*
  • Paxillin / metabolism
  • Phosphorylation
  • Signal Transduction
  • Wound Healing / drug effects
  • rhoA GTP-Binding Protein / metabolism*

Substances

  • Actins
  • Particulate Matter
  • Paxillin
  • RHOA protein, human
  • Focal Adhesion Kinase 1
  • PTK2 protein, human
  • rhoA GTP-Binding Protein