Matrix metalloproteinases of normal human tissues

被引:38
作者
Khasigov, PZ
Podobed, OV
Ktzoeva, SA
Gatagonova, TM
Grachev, SV
Shishkin, SS
Berezov, TT
机构
[1] Sechenov Moscow Med Acad, Moscow 119881, Russia
[2] Russian Acad Med Sci, Med Genet Res Ctr, Moscow 115478, Russia
[3] Patrice Lumumba Peoples Friendship Univ, Moscow 117198, Russia
关键词
matrix metalloproteinases; tissue inhibitors of matrix metalloproteinases; extracellular matrix;
D O I
10.1023/A:1002879128392
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review considers biochemical properties of the family of matrix metalloproteinases (MMPs) of normal human tissues and the involvement of these enzymes in morphogenesis. Four main MMP subfamilies are characterized, and a group of other MMPs is described. Data on mechanisms of activation and inhibition of MMPs in certain tissues during various physiological processes (embryogenesis, angiogenesis, tissue growth and involution) are considered. information about tissue inhibitors of MMP is presented, and the ability of these inhibitors to regulate the activity of MMPs is analyzed.
引用
收藏
页码:130 / 140
页数:11
相关论文
共 124 条
[11]   Membrane-type-2 matrix metalloproteinase can initiate the processing of progelatinase A and is regulated by the tissue inhibitors of metalloproteinases [J].
Butler, GS ;
Will, H ;
Atkinson, SJ ;
Murphy, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 244 (02) :653-657
[12]   Human tissue inhibitor of metalloproteinases 3 interacts with both the N- and C-terminal domains of gelatinases A and B - Regulation by polyanions [J].
Butler, GS ;
Apte, SS ;
Willenbrock, F ;
Murphy, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :10846-10851
[13]   Use of an active-site inhibitor of stromelysin to elucidate the mechanism of prostromelysin activation [J].
Cameron, PM ;
Marcy, AI ;
Rokosz, LL ;
Hermes, JD .
BIOORGANIC CHEMISTRY, 1995, 23 (04) :415-426
[14]   The propeptide domain of membrane type 1 matrix metalloproteinase is required for binding of tissue inhibitor of metalloproteinases and for activation of pro-gelatinase A [J].
Cao, J ;
Drews, M ;
Lee, HM ;
Conner, C ;
Bahou, WF ;
Zucker, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (52) :34745-34752
[15]   Membrane type matrix metalloproteinase 1 activates pro-gelatinase A without furin cleavage of the N-terminal domain [J].
Cao, JA ;
Rehemtulla, A ;
Bahou, W ;
Zucker, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) :30174-30180
[16]   PRIMARY STRUCTURE AND CDNA CLONING OF HUMAN FIBROBLAST COLLAGENASE INHIBITOR [J].
CARMICHAEL, DF ;
SOMMER, A ;
THOMPSON, RC ;
ANDERSON, DC ;
SMITH, CG ;
WELGUS, HG ;
STRICKLIN, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2407-2411
[17]   Induction of tissue inhibitor of metalloproteinases-3 is a delayed early cellular response to hepatocyte growth factor [J].
Castagnino, P ;
Soriano, JV ;
Montesano, R ;
Bottaro, DP .
ONCOGENE, 1998, 17 (04) :481-492
[18]   FIBRONECTIN MATRIX DEPOSITION AND FIBRONECTIN RECEPTOR EXPRESSION IN HEALING AND NORMAL SKIN [J].
CLARK, RAF .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 94 (06) :S128-S134
[19]   Chondrocyte matrix metalloproteinase-8 - Human articular chondrocytes express neutrophil collagenase [J].
Cole, AA ;
Chubinskaya, S ;
Schumacher, B ;
Huch, K ;
CsSzabo, G ;
Yao, J ;
Mikecz, K ;
Hasty, KA ;
Kuettner, KE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) :11023-11026
[20]  
COLLIER IE, 1988, J BIOL CHEM, V263, P6579