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Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model

PURPOSE: Inflammation plays an important role in dry eye syndrome. In this study, inflammatory cytokine expression on the ocular surface in the Botulium toxin B (BTX-B) induced mouse dry eye model was investigated. METHODS: CBA/J mice received an injection of saline or 20 milliunits (mU) of BTX-B in...

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Autores principales: Zhu, Lei, Shen, Jikui, Zhang, Cheng, Park, Choul Yong, Kohanim, Sahar, Yew, Margaret, Parker, John S., Chuck, Roy S.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633460/
https://www.ncbi.nlm.nih.gov/pubmed/19190733
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author Zhu, Lei
Shen, Jikui
Zhang, Cheng
Park, Choul Yong
Kohanim, Sahar
Yew, Margaret
Parker, John S.
Chuck, Roy S.
author_facet Zhu, Lei
Shen, Jikui
Zhang, Cheng
Park, Choul Yong
Kohanim, Sahar
Yew, Margaret
Parker, John S.
Chuck, Roy S.
author_sort Zhu, Lei
collection PubMed
description PURPOSE: Inflammation plays an important role in dry eye syndrome. In this study, inflammatory cytokine expression on the ocular surface in the Botulium toxin B (BTX-B) induced mouse dry eye model was investigated. METHODS: CBA/J mice received an injection of saline or 20 milliunits (mU) of BTX-B into the lacrimal gland. Tear production and corneal fluorescein staining were evaluated in all groups before injection and at 3 time points after. The pro-inflammatory cytokines macrophage inhibitory factor (MIF), interleukin-1β (IL-1 β), tumor necrosis factor-α (TNF- α) and interleukin-6 (IL-6) in conjunctival and corneal epithelium were evaluated by real time quantitative PCR and immunohistochemistry. RESULTS: BTX-B injected mice showed significantly decreased aqueous tear production and increased corneal fluorescein staining at the 1 week and 2 week time points compared with normal control and saline-injected mice. The BTX-B injected mice mRNA expression levels of TNF-α and IL-1β from conjunctival and corneal epithelial cells increased significantly at two early time points comparing with that of normal and saline injected mice, but IL-1β returned to normal levels at the 4 week time point. Saline injected mice showed no difference in mRNA expression of TNF-α, IL-1β, MIF, and IL-6 on the ocular surface tissue at all time points. Immunohistochemistry confirmed these findings. CONCLUSIONS: BTX-B induced mouse model showed decreased aqueous tear production, increased corneal fluorescein staining, and TNF-α and IL-1β increased expression on the ocular surface within one month. The patterns seen appeared to mimic those in humans with non-Sjögren’s syndrome keratoconjunctivitis sicca (NS-KCS).
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spelling pubmed-26334602009-02-02 Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model Zhu, Lei Shen, Jikui Zhang, Cheng Park, Choul Yong Kohanim, Sahar Yew, Margaret Parker, John S. Chuck, Roy S. Mol Vis Research Article PURPOSE: Inflammation plays an important role in dry eye syndrome. In this study, inflammatory cytokine expression on the ocular surface in the Botulium toxin B (BTX-B) induced mouse dry eye model was investigated. METHODS: CBA/J mice received an injection of saline or 20 milliunits (mU) of BTX-B into the lacrimal gland. Tear production and corneal fluorescein staining were evaluated in all groups before injection and at 3 time points after. The pro-inflammatory cytokines macrophage inhibitory factor (MIF), interleukin-1β (IL-1 β), tumor necrosis factor-α (TNF- α) and interleukin-6 (IL-6) in conjunctival and corneal epithelium were evaluated by real time quantitative PCR and immunohistochemistry. RESULTS: BTX-B injected mice showed significantly decreased aqueous tear production and increased corneal fluorescein staining at the 1 week and 2 week time points compared with normal control and saline-injected mice. The BTX-B injected mice mRNA expression levels of TNF-α and IL-1β from conjunctival and corneal epithelial cells increased significantly at two early time points comparing with that of normal and saline injected mice, but IL-1β returned to normal levels at the 4 week time point. Saline injected mice showed no difference in mRNA expression of TNF-α, IL-1β, MIF, and IL-6 on the ocular surface tissue at all time points. Immunohistochemistry confirmed these findings. CONCLUSIONS: BTX-B induced mouse model showed decreased aqueous tear production, increased corneal fluorescein staining, and TNF-α and IL-1β increased expression on the ocular surface within one month. The patterns seen appeared to mimic those in humans with non-Sjögren’s syndrome keratoconjunctivitis sicca (NS-KCS). Molecular Vision 2009-01-30 /pmc/articles/PMC2633460/ /pubmed/19190733 Text en http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhu, Lei
Shen, Jikui
Zhang, Cheng
Park, Choul Yong
Kohanim, Sahar
Yew, Margaret
Parker, John S.
Chuck, Roy S.
Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model
title Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model
title_full Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model
title_fullStr Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model
title_full_unstemmed Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model
title_short Inflammatory cytokine expression on the ocular surface in the Botulium toxin B induced murine dry eye model
title_sort inflammatory cytokine expression on the ocular surface in the botulium toxin b induced murine dry eye model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633460/
https://www.ncbi.nlm.nih.gov/pubmed/19190733
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