Induction of arginases I and II in cornea during herpes simplex virus infection

被引:30
作者
Mistry, SK
Zheng, M
Rouse, BT
Morris, SM [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
[2] Univ Tennessee, Dept Microbiol, Knoxville, TN 37996 USA
关键词
nitric oxide; arginase; herpes; eye disease; ocular;
D O I
10.1016/S0168-1702(00)00243-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Induction of inducible nitric oxide synthase (iNOS) following corneal infection with herpes simplex virus type-1 (HSV-1) generates nitric oxide (NO), an important player in the defense against viral infection. Changes in arginine metabolism during infection are not limited to effects of iNOS but can also involve arginases, which can modulate NO synthesis and produce ornithine for the generation of polyamines and proline. The latter are important molecules involved in tissue damage and repair during inflammation. In this study we determined the responses of arginase I and II in a murine model of HSV-l-induced stromal keratitis (HSK). In the cornea iNOS and arginase II mRNA were co-induced as the initial inflammation developed at 2 days postinfection (p.i.). As stromal keratitis progressed (days 8-15 p.i.) arginase I mRNA was induced tenfold, in contrast to a moderate decrease in arginase II and a loss of iNOS expression. These results suggest that elevated expression of arginase I and II in the cornea at late stages of ocular HSV-I infection may play a role in lesion expression in HSK. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:177 / 182
页数:6
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