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pubmed-article:12393846pubmed:abstractTextIn this report, we demonstrate that herpes simplex virus (HSV) infection of the cornea results in the upregulation of the matrix-degrading metalloproteinase enzyme MMP-9. This enzyme was shown to contribute to the neovascularization process that occurs in the corneal stroma in response to HSV infection. The likely source of MMP-9, at least initially after infection, was neutrophils that were signaled to invade the cornea soon after infection. Corneal infiltrating neutrophils were shown to express MMP-9, and preventing the neutrophil response with specific mAb diminished MMP-9 expression as well as the extent of angiogenesis. Further supporting a role for MMP-9 in HSV-induced corneal angiogenesis was the observation that inhibition of MMP-9 with the specific inhibitor TIMP-1 resulted in reduced angiogenesis. In addition, angiogenesis was diminished in ocularly infected MMP-9 knockout mice. Our results demonstrate that MMP-9 is involved in angiogenesis caused by HSV. Since angiogenesis appears to represent a vital step in the pathogenesis of herpetic stromal keratitis, these results indicate that targeting MMP-9 for inhibition should prove useful for the therapy of herpetic stromal keratitis.lld:pubmed
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pubmed-article:12393846pubmed:articleTitleRole of matrix metalloproteinase-9 in angiogenesis caused by ocular infection with herpes simplex virus.lld:pubmed
pubmed-article:12393846pubmed:affiliationDepartment of Microbiology, The University of Tennessee, Knoxville, Tennessee 37996-0845, USA.lld:pubmed
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pubmed-article:12393846pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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