Contribution of the cornea to cytokine levels in the whole eye induced during the early phase of Pseudomonas aeruginosa challenge
- PMID: 15877609
- DOI: 10.1111/j.1440-1711.2005.01324.x
Contribution of the cornea to cytokine levels in the whole eye induced during the early phase of Pseudomonas aeruginosa challenge
Abstract
Pseudomonas aeruginosa keratitis is one of the most destructive diseases of the cornea. The host response to this infection is critical to the outcome, and is regulated by cytokines produced in the ocular tissue. In this study, we assessed the relative contribution of the cytokines produced in the cornea to the inflammatory response of the whole eye to gain a better understanding of the inflammatory and regulatory processes in the ocular environment during localized corneal infection. C57BL/6 mice were challenged by topical application of P. aeruginosa to wounded corneas. Corneas and whole eyes were harvested 24 h post-challenge and bacterial numbers, myeloperoxidase levels and the levels of cytokines known to be important in keratitis were determined. The site of production of IL-6 and KC in the retina was determined by in situ hybridization. Before infection, 90% of macrophage inflammatory protein (MIP)-2 and approximately 80% of all IFN-gamma and IL-10 produced constitutively in the eye was found outside the cornea. Twenty-four hours after infection, bacterial numbers, levels of myeloperoxidase, and levels of MIP-2 and IL-1 were not different, whether measured in cornea or whole eye. However, expression of IL-6, KC, IFN-gamma and IL-10 was significantly greater in whole eyes than in the corneas of infected eyes. The cells expressing IL-6 and KC in the retina were identified by in situ hybridization. This study indicates that during corneal inflammation, the response of the whole eye as well as the cornea needs to be considered.
Similar articles
-
Gene expression of pro-inflammatory cytokines and chemokines in mouse eye infected with Pseudomonas aeruginosa.Clin Exp Ophthalmol. 2002 Jun;30(3):196-9. doi: 10.1046/j.1442-9071.2002.00510.x. Clin Exp Ophthalmol. 2002. PMID: 12010214
-
Pseudomonas aeruginosa MucD protease mediates keratitis by inhibiting neutrophil recruitment and promoting bacterial survival.Invest Ophthalmol Vis Sci. 2014 Jan 9;55(1):240-6. doi: 10.1167/iovs.13-13151. Invest Ophthalmol Vis Sci. 2014. PMID: 24255043
-
KC production in the cornea in response to Pseudomonas aeruginosa challenge.Immunol Cell Biol. 2000 Feb;78(1):1-4. doi: 10.1046/j.1440-1711.2000.00860.x. Immunol Cell Biol. 2000. PMID: 10651922
-
Corneal response to Pseudomonas aeruginosa infection.Prog Retin Eye Res. 2004 Jan;23(1):1-30. doi: 10.1016/j.preteyeres.2003.10.002. Prog Retin Eye Res. 2004. PMID: 14766315 Review.
-
Pathogenic mechanisms of P. aeruginosa keratitis: a review of the role of T cells, Langerhans cells, PMN, and cytokines.DNA Cell Biol. 2002 May-Jun;21(5-6):383-90. doi: 10.1089/10445490260099665. DNA Cell Biol. 2002. PMID: 12167240 Review.
Cited by
-
Extracellular matrix protein lumican promotes clearance and resolution of Pseudomonas aeruginosa keratitis in a mouse model.PLoS One. 2013;8(1):e54765. doi: 10.1371/journal.pone.0054765. Epub 2013 Jan 24. PLoS One. 2013. PMID: 23358433 Free PMC article.
-
Contributions of MyD88-dependent receptors and CD11c-positive cells to corneal epithelial barrier function against Pseudomonas aeruginosa.Sci Rep. 2017 Oct 23;7(1):13829. doi: 10.1038/s41598-017-14243-w. Sci Rep. 2017. PMID: 29062042 Free PMC article.
-
TLR9 ligand CpG-ODN applied to the injured mouse cornea elicits retinal inflammation.Am J Pathol. 2012 Jan;180(1):209-20. doi: 10.1016/j.ajpath.2011.09.041. Epub 2011 Nov 12. Am J Pathol. 2012. PMID: 22085974 Free PMC article.
-
The ocular pyogranulomatous lesion in a Gentoo penguin (Pygoscelis papua) from the Antarctic Peninsula: evaluation of microbiological and histopathological analysis outcomes.Vet Res Commun. 2021 Sep;45(2-3):143-158. doi: 10.1007/s11259-021-09796-1. Epub 2021 Jun 15. Vet Res Commun. 2021. PMID: 34128178
-
Constitutive and UV-B modulated transcription of Nod-like receptors and their functional partners in human corneal epithelial cells.Mol Vis. 2008 Aug 29;14:1575-83. Mol Vis. 2008. PMID: 18769647 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials