Distinct impact of targeted actin cytoskeleton reorganization on mechanical properties of normal and malignant cells

被引:62
|
作者
Efremov, Yu. M. [1 ]
Dokrunova, A. A. [1 ]
Efremenko, A. V. [1 ]
Kirpichnikov, M. P. [1 ]
Shaitan, K. V. [1 ]
Sokolova, O. S. [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Fac Biol, Moscow 119234, Russia
来源
关键词
AFM; Force spectroscopy; Prostate cancer; Formin; Arp; 2/3; Cortical actin; ATOMIC-FORCE MICROSCOPY; SMALL-MOLECULE INHIBITOR; PROSTATE-CANCER CELLS; ARP2/3; COMPLEX; COLORECTAL-CANCER; AFM INDENTATION; INVASION; CARCINOMA; FORMIN; FIBROBLASTS;
D O I
10.1016/j.bbamcr.2015.05.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The actin cytoskeleton is substantially modified in cancer cells because of changes in actin-binding protein abundance and functional activity. As a consequence, cancer cells have distinctive motility and mechanical properties, which are important for many processes, including invasion and metastasis. Here, we studied the effects of actin cytoskeleton alterations induced by specific nucleation inhibitors (SMIFH2, CK-666), cytochalasin D, Y-27632 and detachment from the surface by trypsinization on the mechanical properties of normal Vero and prostate cancer cell line DU145. The Young's modulus of Vero cells was 1300 +/- 900 Pa, while the prostate cancer cell line DU145 exhibited significantly lower Young's moduli (600 +/- 400 Pa). The Young's moduli exhibited a log-normal distribution for both cell lines. Unlike normal cells, cancer cells demonstrated diverse viscoelastic behavior and different responses to actin cytoskeleton reorganization. They were more resistant to specific formin-dependent nucleation inhibition, and reinforced their cortical actin after detachment from the substrate. This article is part of a Special Issue entitled: Mechanobiology. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:3117 / 3125
页数:9
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