Matrix metalloproteinases and their inhibitors in aqueous humor

被引:34
作者
Huang, SH
Adamis, AP
Wiederschain, DG
Shima, DT
Shing, Y
Moses, MA
机构
[1] MASSACHUSETTS EYE & EAR INFIRM, DEPT OPHTHALMOL, BOSTON, MA 02114 USA
[2] MASSACHUSETTS EYE & EAR INFIRM, CHILDRENS HOSP, DEPT SURG, SURG RES LAB, BOSTON, MA 02114 USA
[3] HARVARD UNIV, SCH MED, DEPT SURG, BOSTON, MA 02115 USA
[4] HARVARD UNIV, SCH MED, PROGRAM CELL & DEV BIOL, BOSTON, MA 02115 USA
关键词
tissue inhibitors of matrix metalloproteinases; extracellular matrix; collagenase inhibitor; DNA synthesis inhibitor; angiogenesis;
D O I
10.1006/exer.1996.0058
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Matrix metalloproteinase activity is the rate-limiting step in extracellular matrix degradation. One mechanism by which metalloproteinases are regulated is through the activity of their endogenous inhibitors, the tissue inhibitors of metalloproteinases. Since metalloproteinase activity is a key component of the angiogenic process and many anterior segment structures are largely avascular, we became interested in examining aqueous humor for the presence of metalloproteinases and their endogenous inhibitors. Using zymography, we have identified the presence of several metalloproteinases in normal aqueous humor. Treatment with 4-aminophenylmercuric acetate, an organomercurial which activates latent metalloproteinases, revealed that all metalloproteinases were in their active state. By Western blot analysis, normal aqueous humor was also found to contain at least two tissue inhibitors of metalloproteinases. Subsequent partial purification by two successive chromatographic steps revealed the presence of inhibitory activity against collagenase, endothelial cell DNA synthesis, and angiogenesis on the chick chorioallantoic membrane. The presence of metalloproteinases and their inhibitors in normal aqueous humor, a fluid which bathes avascular ocular structures, suggests that future studies should examine whether an imbalance in this protease/inhibitor family may contribute to the anterior chamber extracellular matrix alterations associated with diseases such as ocular neovascularization and glaucoma. (C) 1996 Academic Press Limited.
引用
收藏
页码:481 / 489
页数:9
相关论文
共 49 条
[1]  
ANDO H, 1993, INVEST OPHTH VIS SCI, V34, P3541
[2]   CLONING OF THE CDNA-ENCODING HUMAN TISSUE INHIBITOR OF METALLOPROTEINASES-3 (TIMP-3) AND MAPPING OF THE TIMP3 GENE TO CHROMOSOME-22 [J].
APTE, SS ;
MATTEI, MG ;
OLSEN, BR .
GENOMICS, 1994, 19 (01) :86-90
[3]   ROLE OF MATRIX METALLOPROTEINASES IN HUMAN PERIODONTAL-DISEASES [J].
BIRKEDALHANSEN, H .
JOURNAL OF PERIODONTOLOGY, 1993, 64 (05) :474-484
[4]   CDNA CLONING AND EXPRESSION OF A METALLOPROTEINASE INHIBITOR RELATED TO TISSUE INHIBITOR OF METALLOPROTEINASES [J].
BOONE, TC ;
JOHNSON, MJ ;
DECLERCK, YA ;
LANGLEY, KE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) :2800-2804
[5]  
BRAUNHUT SJ, 1994, J BIOL CHEM, V269, P13472
[6]   METALLOPROTEINASE INHIBITORS FROM BOVINE CARTILAGE AND BODY-FLUIDS [J].
BUNNING, RAD ;
MURPHY, G ;
KUMAR, S ;
PHILLIPS, P ;
REYNOLDS, JJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 139 (01) :75-80
[7]   A NEW CLASS OF STEROIDS INHIBITS ANGIOGENESIS IN THE PRESENCE OF HEPARIN OR A HEPARIN FRAGMENT [J].
CRUM, R ;
SZABO, S ;
FOLKMAN, J .
SCIENCE, 1985, 230 (4732) :1375-1378
[8]   EVIDENCE FOR METALLOPROTEINASE AND METALLOPROTEINASE INHIBITOR IMBALANCE IN HUMAN OSTEOARTHRITIC CARTILAGE [J].
DEAN, DD ;
MARTELPELLETIER, J ;
PELLETIER, JP ;
HOWELL, DS ;
WOESSNER, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (02) :678-685
[9]   GROWTH INHIBITORY ACTIVITIES IN AVASCULAR TISSUES ARE RECOGNIZED BY ANTI-TRANSFORMING GROWTH-FACTOR-BETA ANTIBODIES [J].
EISENSTEIN, R ;
GRANTBERTACCHINI, D .
CURRENT EYE RESEARCH, 1991, 10 (02) :157-162
[10]  
FIEGEL VD, 1988, FASEB J, V2, pA1601