Human corneal epithelial cells express functional PAR-1 and PAR-2

Invest Ophthalmol Vis Sci. 2003 Jan;44(1):99-105. doi: 10.1167/iovs.02-0357.

Abstract

Purpose: The objective of this study was to examine whether HCECs express functional proteinase-activated receptor (PAR)-1 and -2 and evaluate the effects of receptor activation on corneal epithelial cell proinflammatory cytokine production.

Methods: Expression of PAR-1 and -2 mRNAs was determined by RT-PCR in cultured primary human corneal epithelial cells (HCECs) and the human corneal epithelial cell line HCE-T. Localization of PAR-1 and -2 in whole normal human corneas was determined by immunofluorescence with PAR-1 and -2 antibodies. The functional competence of PAR-1 and -2 in corneal epithelial cells was assessed by measuring the rapid induction of intracellular [Ca(2+)] in response to thrombin, trypsin, and specific receptor-activating peptides derived from the tethered ligands of the PAR receptors. HCE-T expression of cytokines (IL-6, IL-8, and TNFalpha) in response to activation of PAR-1 and -2 was measured by quantitative RT-PCR and ELISA.

Results: Functional PAR-1 and -2 were expressed in both HCECs and HCE-T cells. Immunoreactivity for PAR-1 and -2 was detected in the outer epithelial layer of the cornea in whole human corneal sections. Activation of PAR-1 and -2 led to upregulation in HCE-T cells of both expression of mRNA and secretion of the proinflammatory cytokines IL-6, IL-8, and TNFalpha.

Conclusions: The results show for the first time that functional PAR-1 and -2 are present in human cornea. Activation of these receptors results in the production of various corneal epithelial cell proinflammatory cytokines. These observations indicate that PAR-1 and -2 may play an important role in modulating corneal inflammatory and wound-healing responses. These receptors may be useful therapeutic targets in several corneal disease processes.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Calcium / metabolism
  • Cell Line
  • Cornea / metabolism*
  • Cytokines / biosynthesis
  • DNA Primers / chemistry
  • Enzyme-Linked Immunosorbent Assay
  • Epithelial Cells / metabolism
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Molecular Sequence Data
  • RNA, Messenger / metabolism
  • Receptor, PAR-1
  • Receptor, PAR-2
  • Receptors, Thrombin / genetics*
  • Receptors, Thrombin / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Thrombin / pharmacology
  • Trypsin / pharmacology
  • Up-Regulation

Substances

  • Cytokines
  • DNA Primers
  • RNA, Messenger
  • Receptor, PAR-1
  • Receptor, PAR-2
  • Receptors, Thrombin
  • Trypsin
  • Thrombin
  • Calcium