UTILIZATION OF TRANSGENIC MICE IN THE STUDY OF MATRIX-DEGRADING PROTEINASES AND THEIR INHIBITORS

被引:18
作者
KHOKHA, R [1 ]
MARTIN, DC [1 ]
FATA, JE [1 ]
机构
[1] UNIV WESTERN ONTARIO,LONDON REG CANC CTR,DEPT BIOCHEM,LONDON,ON N6A 4L6,CANADA
关键词
METALLOPROTEINASES; SERINE PROTEINASES; PROTEINASE INHIBITORS; EXTRACELLULAR MATRIX; TRANSGENIC MICE;
D O I
10.1007/BF00665794
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The extracellular matrix (ECM) acts as both a structural scaffold and an informational medium. Its dynamic status is determined by cells that secrete its constituent molecules and, in most cases, also secrete enzymes that catalyze degradation of these molecules. A stasis between ECM degrading enzymes and their inhibitors maintains the integrity of the matrix. While controlled ECM remodelling is fundamental to several normal processes, uncontrolled disruption underlies diverse pathological conditions. Transgenic mice with specific modulations or a total lack of expression of certain metalloproteinases, serine proteinases or their inhibitors have been generated to elucidate endogenous expression patterns, identify regulatory elements of these genes, and study the physiological consequences of their deregulated expression. With these models we enhance our understanding of the role of proteinases and their inhibitors in diverse normal processes and pathologies including mammary gland development, hemostasis, emphysema and cancer.
引用
收藏
页码:97 / 111
页数:15
相关论文
共 111 条
[31]   A GROWTH-RESPONSIVE GENE (16C8) IN NORMAL MOUSE FIBROBLASTS HOMOLOGOUS TO A HUMAN COLLAGENASE INHIBITOR WITH ERYTHROID-POTENTIATING ACTIVITY - EVIDENCE FOR INDUCIBLE AND CONSTITUTIVE TRANSCRIPTS [J].
EDWARDS, DR ;
WATERHOUSE, P ;
HOLMAN, ML ;
DENHARDT, DT .
NUCLEIC ACIDS RESEARCH, 1986, 14 (22) :8863-8878
[32]   DEVELOPMENT OF VENOUS OCCLUSIONS IN MICE TRANSGENIC FOR THE PLASMINOGEN-ACTIVATOR INHIBITOR-1 GENE [J].
ERICKSON, LA ;
FICI, GJ ;
LUND, JE ;
BOYLE, TP ;
POLITES, HG ;
MAROTTI, KR .
NATURE, 1990, 346 (6279) :74-76
[33]   DEVELOPMENTAL EXPRESSION OF THE ENDOGENOUS TIMP GENE AND A TIMP-1ACZ FUSION GENE IN TRANSGENIC MICE [J].
FLENNIKEN, AM ;
WILLIAMS, BRG .
GENES & DEVELOPMENT, 1990, 4 (07) :1094-1106
[34]   THE PROTEASE-ANTIPROTEASE BALANCE WITHIN THE HUMAN LUNG - IMPLICATIONS FOR THE PATHOGENESIS OF EMPHYSEMA [J].
GADEK, JE ;
PACHT, ER .
LUNG, 1990, 168 :552-564
[35]   HISTOPATHOLOGY OF ALPHA-1-ANTITRYPSIN LIVER-DISEASE IN A TRANSGENIC MOUSE MODEL [J].
GELLER, SA ;
NICHOLS, WS ;
DYCAICO, MJ ;
FELTS, KA ;
SORGE, JA .
HEPATOLOGY, 1990, 12 (01) :40-47
[36]   HUMAN 72-KILODALTON TYPE-IV COLLAGENASE FORMS A COMPLEX WITH A TISSUE INHIBITOR OF METALLOPROTEASES DESIGNATED TIMP-2 [J].
GOLDBERG, GI ;
MARMER, BL ;
GRANT, GA ;
EISEN, AZ ;
WILHELM, S ;
HE, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (21) :8207-8211
[37]   COLLAGENOLYTIC ACTIVITY DURING MAMMALIAN WOUND REPAIR [J].
GRILLO, HC ;
GROSS, J .
DEVELOPMENTAL BIOLOGY, 1967, 15 (04) :300-+
[38]  
HANSEN HB, 1993, CRIT REV ORAL BIOL M, V4, P197
[39]   Extracellular matrix alters epithelial differentiation [J].
Hay, Elizabeth D. .
CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (06) :1029-1035
[40]   GROWTH-PROMOTING ACTIVITY OF TISSUE INHIBITOR OF METALLOPROTEINASES-1 (TIMP-1) FOR A WIDE-RANGE OF CELLS - A POSSIBLE NEW GROWTH-FACTOR IN SERUM [J].
HAYAKAWA, T ;
YAMASHITA, K ;
TANZAWA, K ;
UCHIJIMA, E ;
IWATA, K .
FEBS LETTERS, 1992, 298 (01) :29-32