Structural biochemistry and activation of matrix metalloproteases

被引:328
作者
Kleiner, David E., Jr. [1 ]
Stevenson, William G. Stetler [1 ]
机构
[1] NCI, Pathol Lab, Bethesda, MD 20892 USA
关键词
D O I
10.1016/0955-0674(93)90040-W
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The degradation of the extracellular matrix is part of many pathological and physiological processes. Of the several proteases involved in extracellular matrix turnover, the plasmin/plasminogen activator system and the family of matrix metalloproteases have received the most attention. Recent investigations in the field of matrix metalloprotease biochemistry have focused on the functions of the various enzyme domains and their interactions with inhibitor domains. Research into physiological activation mechanisms has demonstrated a plasmin/plasminogen activator-metalloprotease cascade, as well as providing an initial characterization of cell surface associated metalloprotease activation.
引用
收藏
页码:891 / 897
页数:7
相关论文
共 45 条
[1]   CELL-MEDIATED DEGRADATION OF TYPE-IV COLLAGEN AND GELATIN FILMS IS DEPENDENT ON THE ACTIVATION OF MATRIX METALLOPROTEINASES [J].
ATKINSON, SJ ;
WARD, RV ;
REYNOLDS, JJ ;
MURPHY, G .
BIOCHEMICAL JOURNAL, 1992, 288 :605-611
[2]   EXPRESSION OF THE STROMELYSIN-3 GENE IN FIBROBLASTIC CELLS OF INVASIVE CARCINOMAS OF THE BREAST AND OTHER HUMAN TISSUES - A REVIEW [J].
BASSET, P ;
WOLF, C ;
CHAMBON, P .
BREAST CANCER RESEARCH AND TREATMENT, 1993, 24 (03) :185-193
[3]   A NOVEL METALLOPROTEINASE GENE SPECIFICALLY EXPRESSED IN STROMAL CELLS OF BREAST CARCINOMAS [J].
BASSET, P ;
BELLOCQ, JP ;
WOLF, C ;
STOLL, I ;
HUTIN, P ;
LIMACHER, JM ;
PODHAJCER, OL ;
CHENARD, MP ;
RIO, MC ;
CHAMBON, P .
NATURE, 1990, 348 (6303) :699-704
[4]   MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250
[5]  
BROWN PD, 1990, CANCER RES, V50, P6184
[6]   CELLULAR ACTIVATION OF THE 72 KDA TYPE-IV PROCOLLAGENASE/TIMP-2 COMPLEX [J].
BROWN, PD ;
KLEINER, DE ;
UNSWORTH, EJ ;
STETLERSTEVENSON, WG .
KIDNEY INTERNATIONAL, 1993, 43 (01) :163-170
[7]   ON THE STRUCTURE AND CHROMOSOME LOCATION OF THE 72-KDA AND 92-KDA HUMAN TYPE-IV COLLAGENASE GENES [J].
COLLIER, IE ;
BRUNS, GAP ;
GOLDBERG, GI ;
GERHARD, DS .
GENOMICS, 1991, 9 (03) :429-434
[8]   LARGE INHIBITOR OF METALLOPROTEINASES (LIMP) CONTAINS TISSUE INHIBITOR OF METALLOPROTEINASES (TIMP)-2 BOUND TO 72000-MR PROGELATINASE [J].
CURRY, VA ;
CLARK, IM ;
BIGG, H ;
CAWSTON, TE .
BIOCHEMICAL JOURNAL, 1992, 285 :143-147
[9]   CHARACTERIZATION OF THE FUNCTIONAL DOMAIN OF TISSUE INHIBITOR OF METALLOPROTEINASES-2 (TIMP-2) [J].
DECLERCK, YA ;
YEAN, TD ;
LEE, Y ;
TOMICH, JM ;
LANGLEY, KE .
BIOCHEMICAL JOURNAL, 1993, 289 :65-69
[10]  
DECLERCK YA, 1989, J BIOL CHEM, V264, P17445