Sub-micron lateral topography affects endothelial migration by modulation of focal adhesion dynamics

被引:19
作者
Antonini, S. [1 ,2 ]
Meucci, S. [1 ,2 ,3 ]
Jacchetti, E. [1 ,2 ]
Klingauf, M. [3 ,4 ]
Beltram, F. [1 ,2 ]
Poulikakos, D. [4 ]
Cecchini, M. [1 ,2 ]
Ferrari, A. [4 ]
机构
[1] CNR, Ist Nanosci, NEST, I-56126 Pisa, Italy
[2] Scuola Normale Super Pisa, I-56126 Pisa, Italy
[3] Ctr Nanotechnol Innovat NEST, Ist Italiano Tecnol, I-56127 Pisa, Italy
[4] Swiss Fed Inst Technol, Dept Mech & Proc Engn, Lab Thermodynam Emerging Technol, CH-8092 Zurich, Switzerland
关键词
focal adhesion; nanograting; contact guidance; migration; endothelial cell; CELL-ADHESION; NEURONAL DIFFERENTIATION; VINCULIN RECRUITMENT; NANOSCALE; JUNCTIONS; CONTRACTILITY; ACTIVATION; FORCE;
D O I
10.1088/1748-6041/10/3/035010
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Through the interaction with topographical features, endothelial cells tune their ability to populate target substrates, both in vivo and in vitro. Basal textures interfere with the establishment and maturation of focal adhesions (FAs) thus inducing specific cell-polarization patterns and regulating a plethora of cell activities that govern the overall endothelial function. In this study, we analyze the effect of topographical features on FAs in primary human endothelial cells. Reported data demonstrate a functional link between FA dynamics and cell polarization and spreading on structured substrates presenting variable lateral feature size. Our results reveal that gratings with 2 mu m lateral periodicity maximize contact guidance. The effect is linked to the dynamical state of FAs. We argue that these results are readily applicable to the rational design of active surfaces at the interface with the blood stream.
引用
收藏
页数:8
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