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细胞和组织变形测量:与位移梯度三阶逼近相关的纹理相关性。

Cell and tissue deformation measurements: texture correlation with third-order approximation of displacement gradients.

机构信息

Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.

出版信息

J Biomech. 2013 Sep 27;46(14):2490-6. doi: 10.1016/j.jbiomech.2013.07.035. Epub 2013 Aug 7.

Abstract

Cells remarkably are capable of large deformations during motility and when subjected to mechanical force. Measurement of mechanical deformation (i.e. displacements, strain) is critical to understand functional changes in cells and biological tissues following disease, and to elucidate basic relationships between applied force and cellular biosynthesis. Microscopy-based imaging modalities provide the ability to noninvasively visualize small cell or tissue structures and track their motion over time, often using two-dimensional (2D) digital image (texture) correlation algorithms. For the measurement of complex and nonlinear motion in cells and tissues, implementation of texture correlation algorithms with high order approximations of displacement mapping terms are needed to minimize error. Here, we extend a texture correlation algorithm with up to third-order approximation of displacement mapping terms for the measurement of cell and tissue deformation. We additionally investigate relationships between measurement error and image texture, defined by subset entropy. Displacement measurement error is significantly reduced when the order of displacement mapping terms in the texture correlation algorithm matches or exceeds the order of the deformation observed. Displacement measurement error is also inversely proportional to subset entropy, with well-defined cell and tissue structures leading to high entropy and low error. For cell and tissue studies where complex or nonlinear displacements are expected, texture correlation algorithms with high order terms are required to best characterize the observed deformation.

摘要

细胞在运动和受到机械力时具有显著的大变形能力。测量力学变形(即位移、应变)对于理解疾病后细胞和生物组织的功能变化以及阐明施加力与细胞生物合成之间的基本关系至关重要。基于显微镜的成像方式提供了非侵入性地可视化小细胞或组织结构并跟踪其随时间运动的能力,通常使用二维(2D)数字图像(纹理)相关算法。对于细胞和组织中复杂和非线性运动的测量,需要实现具有位移映射项高阶近似的纹理相关算法,以最小化误差。在这里,我们扩展了一个具有高达三阶位移映射项近似的纹理相关算法,用于测量细胞和组织的变形。我们还研究了测量误差与图像纹理之间的关系,该图像纹理由子集熵定义。当纹理相关算法中的位移映射项的阶数与观察到的变形的阶数匹配或超过时,位移测量误差会显著降低。位移测量误差还与子集熵成反比,具有明确定义的细胞和组织结构会导致高熵和低误差。对于预计会出现复杂或非线性位移的细胞和组织研究,需要使用高阶项的纹理相关算法来最好地描述观察到的变形。

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