Plasticity of cell migration: a multiscale tuning model

被引:1023
作者
Friedl, Peter [1 ,2 ,3 ]
Wolf, Katarina [1 ]
机构
[1] Radboud Univ Nijmegen, Nijmegen Ctr Mol Life Sci, Dept Cell Biol, NL-6500 HB Nijmegen, Netherlands
[2] Univ Wurzburg, Rudolf Virchow Ctr, Deutsch Forsch Gemeinschaft Res Ctr Expt Biomed, D-97980 Wurzburg, Germany
[3] Univ Wurzburg, Dept Dermatol, D-97980 Wurzburg, Germany
关键词
NEURAL CREST CELLS; EXTRACELLULAR-MATRIX; COLLAGEN MATRICES; INTEGRIN FUNCTION; CONTACT GUIDANCE; PERICELLULAR PROTEOLYSIS; AMEBOID MOVEMENT; FOCAL ADHESIONS; SHAPE CHANGE; TUMOR-CELLS;
D O I
10.1083/jcb.200909003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell migration underlies tissue formation, maintenance, and regeneration as well as pathological conditions such as cancer invasion. Structural and molecular determinants of both tissue environment and cell behavior define whether cells migrate individually (through amoeboid or mesenchymal modes) or collectively. Using a multiparameter tuning model, we describe how dimension, density, stiffness, and orientation of the extracellular matrix together with cell determinants-including cell-cell and cell-matrix adhesion, cytoskeletal polarity and stiffness, and pericellular proteolysis-interdependently control migration mode and efficiency. Motile cells integrate variable inputs to adjust interactions among themselves and with the matrix to dictate the migration mode. The tuning model provides a matrix of parameters that control cell movement as an adaptive and interconvertible process with relevance to different physiological and pathological contexts.
引用
收藏
页码:11 / 19
页数:9
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