Modulation of corneal epithelial innate immune response to pseudomonas infection by flagellin pretreatment

Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4664-70. doi: 10.1167/iovs.07-0473.

Abstract

Purpose: A prior study showed that Toll-like receptor (TLR)-5 recognizes Pseudomonas aeruginosa flagellin and triggers the production of proinflammatory cytokines in human corneal epithelial cells (HCECs). The present study was conducted to determine how the inflammatory response is modulated after TLR activation in HCECs.

Methods: HUCL cells, a telomerase-immortalized HCEC line, and primary cultures of HCECs were pretreated with low-dose flagellin and then challenged, with either a high dose of flagellin or with Pseudomonas. NF-kappaB activation was determined by the extent of IkappaB-alpha phosphorylation and degradation and of nuclear p65 DNA binding. The amount of cytokines in the culture media was assessed by ELISA. The activation of p38 and JNK and the cellular expression of TLR5 were determined by Western blot analysis. Cell surface distribution of TLR5 was assessed by flow cytometry. The expression and secretion of antimicrobial peptides were assessed by semiquantitative RT-PCR and slot-blot analysis, respectively.

Results: Pre-exposure (12-24 hours) of HCECs to low-dose flagellin induced a state of tolerance, characterized by impaired activation of the NF-kappaB, p38, and JNK pathways and reduced production of IL-8 and TNF-alpha on subsequent challenge with a high dose of flagellin. Flagellin-induced tolerance did not alter the cellular level and surface distribution of TLR5. Furthermore, flagellin priming of HCECs dampened the inflammatory response of HCECs to live Pseudomonas. Pseudomonas-induced upregulation of antimicrobial genes such as hBD2 and LL-37 was augmented, even in tolerized HCECs.

Conclusions: Pre-exposure of the ocular surface to TLR agonists may induce protective mechanisms that not only modulate the host inflammatory response but also provide an innate defense against bacterial infection in the cornea.

Publication types

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

MeSH terms

  • Antimicrobial Cationic Peptides / genetics
  • Blotting, Western
  • Cathelicidins
  • Cell Line
  • Cytokines / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Epithelium, Corneal / drug effects*
  • Epithelium, Corneal / immunology
  • Flagellin / pharmacology*
  • Flow Cytometry
  • Humans
  • I-kappa B Proteins / metabolism
  • Immunity, Innate*
  • Immunoblotting
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism
  • Phosphorylation
  • Pseudomonas Infections / immunology*
  • Pseudomonas aeruginosa / physiology
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Toll-Like Receptor 5 / metabolism
  • beta-Defensins / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Cytokines
  • DEFB4A protein, human
  • I-kappa B Proteins
  • NF-kappa B
  • NFKBIA protein, human
  • RNA, Messenger
  • TLR5 protein, human
  • Toll-Like Receptor 5
  • beta-Defensins
  • Flagellin
  • NF-KappaB Inhibitor alpha
  • JNK Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Cathelicidins