Lipopolysaccharide regulation of Toll-like receptor-4 and matrix metalloprotease-9 in human primary corneal fibroblasts
Lipopolysaccharide regulation of Toll-like receptor-4 and matrix metalloprotease-9 in human primary corneal fibroblasts
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, GM-CSF, IFNγ, and TNFα 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.
2796-2803
Wong, Yuk
744079fa-97e7-46aa-ab38-d825481d45f3
Sethu, Claire
eb72b789-c06a-41f6-a5a2-866153526001
Louafi, Fethi
4c37a7a6-5fd5-4c4b-b0ee-7042da09e273
Hossain, Parwez
563de5fc-84ad-4539-9228-bde0237eaf51
1 April 2011
Wong, Yuk
744079fa-97e7-46aa-ab38-d825481d45f3
Sethu, Claire
eb72b789-c06a-41f6-a5a2-866153526001
Louafi, Fethi
4c37a7a6-5fd5-4c4b-b0ee-7042da09e273
Hossain, Parwez
563de5fc-84ad-4539-9228-bde0237eaf51
Wong, Yuk, Sethu, Claire, Louafi, Fethi and Hossain, Parwez
(2011)
Lipopolysaccharide regulation of Toll-like receptor-4 and matrix metalloprotease-9 in human primary corneal fibroblasts.
Investigative Ophthalmology & Visual Science, 52 (5), .
(doi:10.1167/iovs.10-5459).
(PMID:21220558)
Abstract
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, GM-CSF, IFNγ, and TNFα 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.
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Published date: 1 April 2011
Organisations:
Infection Inflammation & Immunity
Identifiers
Local EPrints ID: 181591
URI: http://eprints.soton.ac.uk/id/eprint/181591
ISSN: 0146-0404
PURE UUID: 6b3181ee-ee65-49f1-bf66-69fb23e42cf4
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Date deposited: 18 Apr 2011 13:53
Last modified: 15 Mar 2024 03:24
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Author:
Yuk Wong
Author:
Claire Sethu
Author:
Fethi Louafi
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