MT1-MMP: A potent modifier of pericellular microenvironment

被引:409
作者
Itoh, Y
Seiki, M
机构
[1] Univ Tokyo, Inst Med Sci, Div Canc Cell Res, Tokyo 1088639, Japan
[2] Univ London Imperial Coll Sci & Technol, Kennedy Inst, Div Rheumatol, London, England
关键词
D O I
10.1002/jcp.20431
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cells are regulated by many different means, and there is more and more evidence emerging that changes in the microenvironment greatly affect cell function. MT1-MMP is a type 1 transmembrane proteinase which participates in pericellular proteolysis of extracellular matrix,(ECM) macromolecules. The enzyme is cellular collagenase essential for skeletal development, cancer invasion, growth, and angiogenesis. MT1-MMP promotes cell invasion and motility by pericellular ECM degradation, shedding of CD44 and syndecan 1, and by activating ERK. Thus MT1-MMP is one of the factors that influence the cellular microenvironment and thereby affect cell-signaling pathways and eventually alters cellular behavior. As a proteinase, MT1-MMP is regulated by inhibitors, but it also requires formation of a homo-oligomer complex, localization to migration front of the cells, and internalization to become a "functionally active" cell function modifier. Developing new means to inhibit "functional activity" of MT1-MMP may be a new direction to establish treatments for the diseases that MT1-MMP mediates such as cancer and rheumatoid arthritis.
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页码:1 / 8
页数:8
相关论文
共 92 条
  • [1] The syndecan-1 ectodomain regulates αvβ3 integrin activity in human mammary carcinoma cells
    Beauvais, DLM
    Burbach, BJ
    Rapraeger, AC
    [J]. JOURNAL OF CELL BIOLOGY, 2004, 167 (01) : 171 - 181
  • [2] Matrix-dependent proteolysis of surface transglutaminase by membrane-type metalloproteinase regulates cancer cell adhesion and locomotion
    Belkin, AM
    Akimov, SS
    Zaritskaya, LS
    Ratnikov, BI
    Deryugina, EI
    Strongin, AY
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (21) : 18415 - 18422
  • [3] Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis
    Bergers, G
    Brekken, R
    McMahon, G
    Vu, TH
    Itoh, T
    Tamaki, K
    Tanzawa, K
    Thorpe, P
    Itohara, S
    Werb, Z
    Hanahan, D
    [J]. NATURE CELL BIOLOGY, 2000, 2 (10) : 737 - 744
  • [4] Bigg HF, 2001, CANCER RES, V61, P3610
  • [5] Timeline - Matrix metalloproteinases: a tail of a frog that became a prince
    Brinckerhoff, CE
    Matrisian, LM
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (03) : 207 - 214
  • [6] Disruption of angiogenesis by PEX, a noncatalytic metalloproteinase fragment with integrin binding activity
    Brooks, PC
    Silletti, S
    von Schalscha, TL
    Friedlander, M
    Cheresh, DA
    [J]. CELL, 1998, 92 (03) : 391 - 400
  • [7] The TIMP2 membrane type 1 metalloproteinase "receptor" regulates the concentration and efficient activation of progelatinase A - A kinetic study
    Butler, GS
    Butler, MJ
    Atkinson, SJ
    Will, H
    Tamura, T
    van Westrum, SS
    Crabbe, T
    Clements, J
    d'Ortho, MP
    Murphy, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (02) : 871 - 880
  • [8] Distinct roles for the catalytic and hemopexin domains of membrane type 1-matrix metalloproteinase in substrate degradation and cell migration
    Cao, J
    Kozarekar, P
    Pavlaki, M
    Chiarelli, C
    Bahou, WF
    Zucker, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (14) : 14129 - 14139
  • [9] THE C-TERMINAL REGION OF MEMBRANE TYPE MATRIX METALLOPROTEINASE IS A FUNCTIONAL TRANSMEMBRANE DOMAIN REQUIRED FOR PRO-GELATINASE-C ACTIVATION
    CAO, J
    SATO, H
    TAKINO, T
    SEIKI, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (02) : 801 - 805
  • [10] MT1-MMP-dependent neovessel formation within the confines of the three-dimensional extracellular matrix
    Chun, TH
    Sabeh, F
    Ota, I
    Murphy, H
    McDonagh, KT
    Holmbeck, K
    Birkedal-Hansen, H
    Allen, ED
    Weiss, SJ
    [J]. JOURNAL OF CELL BIOLOGY, 2004, 167 (04) : 757 - 767