Abstract

Analysis of cell mobility is a key issue for abnormality identification and classification in cell biology research. However, since cell deformation induced by various biological processes is random and cell protrusion is irregular, it is difficult to measure cell morphology and motility in microscopic images. To address this dilemma, we propose an improved variation optical flow model for quantitative analysis of intracellular motility, which not only extracts intracellular motion fields effectively but also deals with optical flow computation problem at the border by taking advantages of the formulation based on L1 and L2 norm, respectively. In the energy functional of our proposed optical flow model, the data term is in the form of L2 norm; the smoothness of the data changes with regional features through an adaptive parameter, using L1 norm near the edge of the cell and L2 norm away from the edge. We further extract histograms of oriented optical flow (HOOF) after optical flow field of intracellular motion is computed. Then distances of different HOOFs are calculated as the intracellular motion features to grade the intracellular motion. Experimental results show that the features extracted from HOOFs provide new insights into the relationship between the cell motility and the special pathological conditions.

Highlights

  • Cell morphology and mobility indicate physiological and pathological characters of the organism [1]

  • We proposed a novel scheme for quantitative analysis of intracellular motility based on the variation optical flow model

  • We applied improved variation optical flow model to visualize the velocity of intracellular motion and further coded the velocity by color, as shown in Figures 1 and 2

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Summary

Introduction

Cell morphology and mobility indicate physiological and pathological characters of the organism [1]. It has been demonstrated that quantitative analysis of cell morphology and mobility offers the possibility to improve our understanding of the biological processes at the cellular level [2]. Estimation of live cell mobility for analyzing dynamic properties of biological and pathological phenomena has been extensively used in clinical diagnosis and biological research, including inflammation research, drug test, wound healing, tumor genesis, and immune response [3,4,5,6,7]. Life information under special condition is to be uncovered by quantitative analysis of intracellular motility. It is difficult to measure intracellular motility due to irregular complicated cell deformation. We proposed a novel approach for quantitative analysis of intracellular motility based on optical flow model

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