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本文引用的文献

1
Soft matters in cell adhesion: rigidity sensing on soft elastic substrates.细胞黏附中的软物质:软弹性基质上的刚性传感
Soft Matter. 2007 Feb 14;3(3):263-266. doi: 10.1039/b606409d.
2
Mechanosensing in actin stress fibers revealed by a close correlation between force and protein localization.肌动蛋白应力纤维中的机械传感通过力与蛋白质定位之间的紧密相关性得以揭示。
J Cell Sci. 2009 May 15;122(Pt 10):1665-79. doi: 10.1242/jcs.042986. Epub 2009 Apr 28.
3
Cell traction forces direct fibronectin matrix assembly.细胞牵引力引导纤连蛋白基质组装。
Biophys J. 2009 Jan;96(2):729-38. doi: 10.1016/j.bpj.2008.10.009.
4
Traction stress in focal adhesions correlates biphasically with actin retrograde flow speed.粘着斑中的牵引应力与肌动蛋白逆行流动速度呈双相相关。
J Cell Biol. 2008 Dec 15;183(6):999-1005. doi: 10.1083/jcb.200810060.
5
High resolution traction force microscopy based on experimental and computational advances.基于实验和计算进展的高分辨率牵引力显微镜。
Biophys J. 2008 Jan 1;94(1):207-20. doi: 10.1529/biophysj.107.113670. Epub 2007 Sep 7.
6
Cell-matrix adhesion.细胞-基质黏附
J Cell Physiol. 2007 Dec;213(3):565-73. doi: 10.1002/jcp.21237.
7
Microfabricated silicone elastomeric post arrays for measuring traction forces of adherent cells.用于测量贴壁细胞牵引力的微加工硅橡胶弹性柱阵列
Methods Cell Biol. 2007;83:313-28. doi: 10.1016/S0091-679X(07)83013-5.
8
Cell traction force and measurement methods.细胞牵引力及测量方法。
Biomech Model Mechanobiol. 2007 Nov;6(6):361-71. doi: 10.1007/s10237-006-0068-4. Epub 2007 Jan 3.
9
Traction forces of fibroblasts are regulated by the Rho-dependent kinase but not by the myosin light chain kinase.成纤维细胞的牵引力受Rho依赖性激酶调节,而非肌球蛋白轻链激酶调节。
Arch Biochem Biophys. 2006 Dec 15;456(2):224-31. doi: 10.1016/j.abb.2006.09.025. Epub 2006 Oct 11.
10
Nonmuscle myosin IIA-dependent force inhibits cell spreading and drives F-actin flow.非肌肉肌球蛋白IIA依赖性力抑制细胞铺展并驱动F-肌动蛋白流动。
Biophys J. 2006 Nov 15;91(10):3907-20. doi: 10.1529/biophysj.106.084806. Epub 2006 Aug 18.

优化牵引力显微镜以研究微米级焦点黏附。

Optimization of traction force microscopy for micron-sized focal adhesions.

机构信息

Physics Department, James Franck Institute and Institute for Biophysical Dynamics, University of Chicago, Chicago, IL, USA.

出版信息

J Phys Condens Matter. 2010 May 19;22(19):194104. doi: 10.1088/0953-8984/22/19/194104.

DOI:10.1088/0953-8984/22/19/194104
PMID:20523913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2879600/
Abstract

To understand how adherent cells regulate traction forces on their surrounding extracellular matrix (ECM), quantitative techniques are needed to measure forces at the cell-ECM interface. Microcontact printing is used to create a substrate of 1 μm diameter circles of ECM ligand to experimentally study the reconstruction of traction stresses at constrained, point-like focal adhesions. Traction reconstruction with point forces (TRPF) and Fourier transform traction cytometry (FTTC) are used to calculate the traction forces and stress field, respectively, at isolated adhesions. We find that the stress field calculated with FTTC peaks near the center of individual adhesions but propagates several microns beyond the adhesion location. We find the optimal set of FTTC parameters that yield the highest stress magnitude, minimizing information lost from over-smoothing and sampling of the displacement or stress field. A positive correlation between the TRPF and FTTC measurements exists, but integrating the FTTC stress field over the adhesion area yields only a small fraction of the force calculated by TRPF. An effective area similar to that defined by the width of the stress distribution measured with FTTC is required to reconcile these measurements. These measurements set bounds on the spatial resolution and precision of FTTC measurements on micron-sized adhesions.

摘要

为了了解贴壁细胞如何调节其周围细胞外基质(ECM)上的牵引力,需要定量技术来测量细胞-ECM 界面上的力。微接触印刷用于创建 ECM 配体的 1μm 直径圆圈的基底,以实验研究约束点状黏附点处牵引力的重建。使用点力牵引力重建(TRPF)和傅里叶变换牵引力细胞术(FTTC)分别计算孤立黏附点处的牵引力和应力场。我们发现,FTTC 计算出的应力场在单个黏附点的中心附近达到峰值,但在黏附位置之外传播了几个微米。我们找到了一组最佳的 FTTC 参数,这些参数产生了最大的应力幅度,同时最小化了由于过度平滑和对位移或应力场的采样而导致的信息丢失。TRPF 和 FTTC 测量之间存在正相关关系,但将 FTTC 应力场积分到黏附区域仅产生 TRPF 计算出的力的一小部分。需要类似于 FTTC 测量的应力分布宽度定义的有效区域来协调这些测量。这些测量为微米大小的黏附点上的 FTTC 测量的空间分辨率和精度设定了界限。