Cellular strategies for proteolytic targeting during migration and invasion

被引:43
作者
Ellis, V [1 ]
Murphy, G [1 ]
机构
[1] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
serine proteinase; metalloproteinase; cell membrane; extracellular matrix; migration;
D O I
10.1016/S0014-5793(01)02845-9
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
Cell migration over or through the extracellular matrix (ECM) is an integral feature of both physiological and pathological processes. Regulation of the changing cell-ECM interactions involved can be effected by proteolysis and requires strict spatial and temporal targeting of proteinase activity. The versatile use of different proteinase systems, with a variety of localisation mechanisms and cleavage targets, is being revealed by a plethora of studies using in vitro models. This mini review reflects the status of our knowledge of strategies for the localisation of proteolytic activity effected during cell migration.(C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science BN. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
相关论文
共 69 条
[1]   Membrane type 1 matrix metalloproteinase and gelatinase A synergistically degrade type 1 collagen in a cell model [J].
Atkinson, SJ ;
Patterson, ML ;
Butler, MJ ;
Murphy, G .
FEBS LETTERS, 2001, 491 (03) :222-226
[2]   The plasminogen activator inhibitor PAI-1 controls in vivo tumor vascularization by interaction with proteases, not vitronectin:: Implications for antiangiogenic strategies [J].
Bajou, K ;
Masson, V ;
Gerard, RD ;
Schmitt, PM ;
Albert, V ;
Praus, M ;
Lund, LR ;
Frandsen, TL ;
Brunner, N ;
Dano, K ;
Fusenig, NE ;
Weidle, U ;
Carmeliet, G ;
Loskutoff, D ;
Collen, D ;
Carmeliet, P ;
Foidart, JM ;
Noël, AS .
JOURNAL OF CELL BIOLOGY, 2001, 152 (04) :777-784
[3]   A urokinase receptor-associated protein with specific collagen binding properties [J].
Behrendt, N ;
Jensen, ON ;
Engelholm, LH ;
Mortz, E ;
Mann, M ;
Dano, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (03) :1993-2002
[4]   Membrane-type 1 matrix metalloprotease (MT1-MMP) enables invasive migration of glioma cells in central nervous system white matter [J].
Beliën, ATJ ;
Paganetti, PA ;
Schwab, ME .
JOURNAL OF CELL BIOLOGY, 1999, 144 (02) :373-384
[5]   Remarkable roles of proteolysis on and beyond the cell surface [J].
Blobel, CP .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (05) :606-612
[6]   THE ASTACIN FAMILY OF METALLOENDOPEPTIDASES [J].
BOND, JS ;
BEYNON, RJ .
PROTEIN SCIENCE, 1995, 4 (07) :1247-1261
[7]  
Bourguignon LYW, 1998, J CELL PHYSIOL, V176, P206, DOI 10.1002/(SICI)1097-4652(199807)176:1<206::AID-JCP22>3.3.CO
[8]  
2-S
[9]   Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alpha v beta 3 [J].
Brooks, PC ;
Stromblad, S ;
Sanders, LC ;
vonSchalscha, TL ;
Aimes, RT ;
StetlerStevenson, WG ;
Quigley, JP ;
Cheresh, DA .
CELL, 1996, 85 (05) :683-693
[10]   THE RECEPTOR FOR UROKINASE-TYPE PLASMINOGEN-ACTIVATOR IS NOT ESSENTIAL FOR MOUSE DEVELOPMENT OR FERTILITY [J].
BUGGE, TH ;
SUH, TT ;
FLICK, MJ ;
DAUGHERTY, CC ;
ROMER, J ;
SOLBERG, H ;
ELLIS, V ;
DANO, K ;
DEGEN, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (28) :16886-16894