April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Toll-like Receptor Mediated Induction of Peptidoglycan Recognition Proteins (PGRPs) in Human Corneal Epithelial Cells
Author Affiliations & Notes
  • P. Ma
    1Ocular Surface Center, Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, Houston, Texas
    2State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun-Yat Sen University, Guangzhou, China
  • Z. Wang
    2State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun-Yat Sen University, Guangzhou, China
  • S. C. Pflugfelder
    1Ocular Surface Center, Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, Houston, Texas
  • D.-Q. Li
    1Ocular Surface Center, Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, Houston, Texas
  • Footnotes
    Commercial Relationships  P. Ma, None; Z. Wang, None; S.C. Pflugfelder, None; D.-Q. Li, None.
  • Footnotes
    Support  DOD CDMRP Grant FY06 PR064719 (DQL), NIH Grant EY11915 (SCP), Research to Prevent Blindness, Oshman Foundation, William Stamps Farish Fund.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 5542. doi:
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      P. Ma, Z. Wang, S. C. Pflugfelder, D.-Q. Li; Toll-like Receptor Mediated Induction of Peptidoglycan Recognition Proteins (PGRPs) in Human Corneal Epithelial Cells. Invest. Ophthalmol. Vis. Sci. 2009;50(13):5542.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Peptidoglycan recognition proteins (PGRPs), a novel family of pattern recognition receptors (PRRs) in innate immunity conserved from insects to mammals, recognize bacterial cell wall peptidoglycan (PG) and act as antibacterial proteins. In humans, four PGRPs (PGRP-S, -L, -I, and -Iβ) have been cloned and all bind PG. In this study, we investigated the expression and regulation of PGRPs in human corneal epithelium in response to microbial ligands.

Methods: : Fresh human corneoscleral tissues from normal donors were used to prepare cryosections for immunostaining. Primary human corneal epithelial cells were established from limbal explants. The confluent cell cultures were treated with 11 microbial components, ligands to toll-like receptors (TLRs) 1-9, for a different time periods (4-48 hours) with or without TLR antibodies or NFkB inhibitors. The mRNA expression of PGRPs was evaluated by RT and real time PCR using TaqMan primers and probes, with GAPDH as an internal control. Their proteins and NF-kB signaling pathway activation were determined by immunofluorescent staining and Western blot.

Results: : PGRP-L, -I, and -Iβ were found to be expressed by human corneal epithelium and primary cultured human corneal epithelial cells. Their mRNA levels peaked at 16 hour in response to the TLR ligands. PGRP-I was the most inducible with its mRNA markedly stimulated by multiple microbial components including Pam3csk4, PG, poly I:C (dsRNA), flagellin and FSL-1, ligands for TLRs 1, 2, 3, 5, and 6. PGRP-L and -Iβ were inducible mainly by poly I:C and flagellin, although they were constitutively expressed at higher levels than PGRP-I in human corneal epithelial cells. The induction of PGRPs was confirmed at the protein levels by immunostaining and Western blot. TLR antibodies, IKK inhibitor II (wedelolactone) or NF-kB activation inhibitor (quinazoline) blocked NF-kB p65 nuclear translocation and phosphorylation, and also suppressed PGRP-I and PGRP-Iβ expression stimulated by Poly I:C or flagellin.

Keywords: cornea: epithelium • inflammation • immunomodulation/immunoregulation 
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