Nano-mechanical single-cell sensing of cell-matrix contacts

被引:6
作者
Zajiczek, Lydia [1 ]
Shaw, Michael [1 ,2 ]
Faruqui, Nilofar [1 ]
Bella, Angelo [1 ]
Pawar, Vijay M. [2 ]
Srinivasan, Mandayam A. [2 ,3 ,4 ]
Ryadnov, Maxim G. [1 ]
机构
[1] Natl Phys Lab, Hampton Rd, Teddington TW11 0LW, Middx, England
[2] UCL, Dept Comp Sci, UCL TouchLab, London WC1E 6BT, England
[3] MIT, Dept Mech Engn, MIT TouchLab, Cambridge, MA 02139 USA
[4] MIT, Elect Res Lab, Cambridge, MA 02139 USA
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
SUBSTRATE STIFFNESS; FORCE; ADHESION; RIGIDITY; FIBRONECTIN; FILOPODIA; AREA; FIBROBLASTS; MICROSCOPY; MORPHOLOGY;
D O I
10.1039/c6nr05667a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Extracellular protein matrices provide a rigidity interface exhibiting nano-mechanical cues that guide cell growth and proliferation. Cells sense such cues using actin-rich filopodia extensions which encourage favourable cell-matrix contacts to recruit more actin-mediated local forces into forming stable focal adhesions. A challenge remains in identifying and measuring these local cellular forces and in establishing empirical relationships between them, cell adhesion and filopodia formation. Here we investigate such relationships using a micromanipulation system designed to operate at the time scale of focal contact dynamics, with the sample frequency of a force probe being 0.1 ms, and to apply and measure forces at nano-to-micro Newton ranges for individual mammalian cells. We explore correlations between cell biomechanics, cell-matrix attachment forces and the spread areas of adhered cells as well as their relative dependence on filopodia formation using synthetic protein matrices with a proven ability to induce enhanced filopodia numbers in adherent cells. This study offers a basis for engineering exploitable cell-matrix contacts in situ at the nanoscale and single-cell levels.
引用
收藏
页码:18105 / 18112
页数:8
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