One-dimensional topography underlies three-dimensional fibrillar cell migration

被引:562
作者
Doyle, Andrew D. [1 ]
Wang, Francis W. [2 ]
Matsumoto, Kazue [1 ]
Yamada, Kenneth M. [1 ]
机构
[1] Natl Inst Dental & Craniofacial Res, Lab Cell & Dev Biol, NIH, Bethesda, MD 20892 USA
[2] Natl Inst Stand & Technol, Div Polymers, Mat Sci & Engn Lab, Gaithersburg, MD 20899 USA
基金
美国国家卫生研究院;
关键词
SELECTIVE STABILIZATION; FIBROBLAST MOVEMENT; FOCAL ADHESIONS; MATRIX; 3D; MICROTUBULES; ATTACHMENT; LOCOMOTION; ACTOMYOSIN; SUBSTRATE;
D O I
10.1083/jcb.200810041
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Current concepts of cell migration were established in regular two-dimensional (2D) cell culture, but the roles of topography are poorly understood for cells migrating in an oriented 3D fibrillar extracellular matrix (ECM). We use a novel micropatterning technique termed microphotopatterning (mu PP) to identify functions for 1D fibrillar patterns in 3D cell migration. In striking contrast to 2D, cell migration in both 1D and 3D is rapid, uniaxial, independent of ECM ligand density, and dependent on myosin II contractility and microtubules (MTs). 1D and 3D migration are also characterized by an anterior MT bundle with a posterior centrosome. We propose that cells migrate rapidly through 3D fibrillar matrices by a 1D migratory mechanism not mimicked by 2D matrices.
引用
收藏
页码:481 / 490
页数:10
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