Extracellular matrix determinants of proteolytic and non-proteolytic cell migration

被引:256
作者
Wolf, Katarina [1 ]
Friedl, Peter [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, Dept Cell Biol, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands
[2] Univ Texas MD Anderson Canc Ctr, David H Koch Ctr Appl Canc Res, Dept Genitourinary Oncol, Houston, TX 77030 USA
关键词
IN-VIVO; COLLAGEN DEGRADATION; BASEMENT-MEMBRANE; PERICELLULAR PROTEOLYSIS; MULTIPHOTON MICROSCOPY; PLASMINOGEN-ACTIVATOR; GENERATION MICROSCOPY; CONTACT GUIDANCE; CROSS-LINKING; CATHEPSIN K;
D O I
10.1016/j.tcb.2011.09.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell invasion into the 3D extracellular matrix (ECM) is a multistep biophysical process involved in inflammation, tissue repair, and metastatic cancer invasion. Migrating cells navigate through tissue structures of complex and often varying physicochemical properties, including molecular composition, porosity, alignment and stiffness, by adopting strategies that involve deformation of the cell and engagement of matrix-degrading proteases. We review how the ECM determines whether or not pericellular proteolysis is required for cell migration, ranging from protease-driven invasion and secondary tissue destruction, to non-proteolytic, non-destructive movement that solely depends on cell deformability and available tissue space. These concepts call for therapeutic targeting of proteases to prevent invasion-associated tissue destruction rather than the migration process per se.
引用
收藏
页码:736 / 744
页数:9
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