Matrix metalloproteinases are down-regulated in rat lenses exposed to oxidative stress

被引:22
作者
John, M
Jaworski, C
Chen, ZG
Subramanian, S
Ma, WC
Sun, F
Li, DY
Spector, A
Carper, D
机构
[1] NEI, Sect Mol Therapeut, NIH, Bethesda, MD 20892 USA
[2] Univ Nacl Colombia, Coll Phys & Surg, Dept Ophthalmol, New York, NY 10032 USA
关键词
MMPs; MT-MMPs; TIMPs; beta-actin; oxidative stress; cataract;
D O I
10.1016/j.exer.2004.08.025
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Matrix metalloproteinases are important biological effectors of tissue remodelling. Increased MMP expression occurs during injury, inflammation, cellular transformation, and oxidative stress. Oxidative stress in the lens, a causal factor in cataractogenesis, has been shown to induce MMP secretion. The objective of this study was to assess the expression of MMPs and their regulators in an oxidative stress model of cataract, where epithelial cell death and cortical fibre cell swelling occurs in rat lenses after exposure to riboflavin, oxygen, and light. Two time points (4 and 7 hr of exposure) were chosen in order to compare transparent lenses with partially opaque lenses. MMP activity, protein, and mRNA levels were measured. The results show that MMP-2, MMP-9, MT1-MMP, and MT3-MMP are down-regulated by oxidative stress and that the down-regulation is most likely due to reduced gene transcription. In contrast, genes for catalase, glutathione peroxidase, and GAPDH are essentially unaffected, while beta-actin mRNA and protein levels are markedly increased at both time points. The down-regulation of MMPs occurs in lenses still seemingly transparent after 4 hr of exposure, indicating that reduced MMP activity is a relatively early response to the oxidative stress. Moreover, in our model system, MMIP inhibition, not induction, is associated with cataractogenesis. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:839 / 846
页数:8
相关论文
共 39 条
[31]   Review: Oxidative stress and disease [J].
Spector, A .
JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS, 2000, 16 (02) :193-201
[32]   MULTIPLE-MODES OF ACTIVATION OF LATENT HUMAN FIBROBLAST COLLAGENASE - EVIDENCE FOR THE ROLE OF A CYS-73 ACTIVE-SITE ZINC COMPLEX IN LATENCY AND A CYSTEINE SWITCH MECHANISM FOR ACTIVATION [J].
SPRINGMAN, EB ;
ANGLETON, EL ;
BIRKEDALHANSEN, H ;
VANWART, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :364-368
[33]   How matrix metalloproteinases regulate cell behavior [J].
Sternlicht, MD ;
Werb, Z .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2001, 17 :463-516
[34]   Induction of matrix metalloproteinases 2 and 9 following stress to the lens [J].
Tamiya, S ;
Wormstone, IM ;
Marcantonio, JM ;
Gavrilovic, J ;
Duncan, G .
EXPERIMENTAL EYE RESEARCH, 2000, 71 (06) :591-597
[35]  
Tsang KJ, 2001, INT J ONCOL, V18, P369
[36]   MATRIX METALLOPROTEINASES AND THEIR INHIBITORS IN CONNECTIVE-TISSUE REMODELING [J].
WOESSNER, JF .
FASEB JOURNAL, 1991, 5 (08) :2145-2154
[37]  
Wormstone IM, 2002, INVEST OPHTH VIS SCI, V43, P2301
[38]   The effect of catalase amplification on immortal lens epithelial cell lines [J].
Yang, YQ ;
Spector, A ;
Ma, WC ;
Wang, RR ;
Larsen, K ;
Kleiman, NJ .
EXPERIMENTAL EYE RESEARCH, 1998, 67 (06) :647-656
[39]   Direct comparison of GAPDH, β-actin, cyclophilin, and 28S rRNA as internal standards for quantifying RNA levels under hypoxia [J].
Zhong, H ;
Simons, JW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 259 (03) :523-526