Lipopolysaccharide Regulation of Toll-Like Receptor-4 and Matrix Metalloprotease-9 in Human Primary Corneal Fibroblasts

被引:29
作者
Wong, Yuk [2 ]
Sethu, Claire [2 ]
Louafi, Fethi [2 ]
Hossain, Parwez [1 ,2 ]
机构
[1] Southampton Gen Hosp, Eye Unit, Southampton SO16 6YD, Hants, England
[2] Univ Southampton, Fac Med, Div Infect Inflammat & Immun, Southampton SO9 5NH, Hants, England
关键词
PSEUDOMONAS-AERUGINOSA INFECTION; CONTACT-LENS WEAR; EPITHELIAL-CELLS; INFLAMMATORY CYTOKINES; TISSUE INHIBITORS; GENE-EXPRESSION; IFN-GAMMA; INDUCTION; KERATITIS; LPS;
D O I
10.1167/iovs.10-5459
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. Toll-like receptor 4 (TLR4) is a key component of the innate immune response related to microbial keratitis (MK). Pathways and downstream effectors relating to TLR signaling remain unknown in human bacterial MK. To this effect, by activating the TLR4 signaling cascade with lipopolysaccharide (LPS), the authors investigated whether TLR4, matrix metalloproteases (MMP)-2, MMP-9, and cytokine expression in diseased human primary corneal fibroblasts (CFs) were altered. METHODS. Human primary CFs from patients with severe corneal ulceration were cultured in conjunction with healthy control CFs and treated with LPS derived from Pseudomonas aeruginosa. RESULTS. TLR4, MMP-2, and MMP-9 were constitutively expressed in both ulcerated and control CFs. Diseased CFs showed greater responsiveness to LPS stimulation. TLR4 and MMP-9 expression was dose-dependently increased by LPS. MMP-2 expression was not affected by LPS. Analysis on cytokine expression revealed that IL-2, IL-8, IL-10, IL-12p70, GMCSF, IFN gamma, and TNF alpha expression increased after LPS treatment but only in diseased cells. CONCLUSIONS. TLR4 activation with LPS increases TLR4, MMP-9, and cytokine expression in CFs cultured from patients with microbial keratitis. Overexpression of these products may provide a local mechanism to eradicate bacterial infection but may also aid corneal ulceration and perforation. (Invest Ophthalmol Vis Sci. 2011; 52: 2796-2803) DOI:10.1167/iovs. 10-5459
引用
收藏
页码:2796 / 2803
页数:8
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