Abstract

We describe a computational framework for the comprehensive assessment of contractile responses of enzymatically dissociated adult cardiac myocytes. The proposed methodology comprises the following stages: digital video recording of the contracting cell, edge preserving total variation-based image smoothing, segmentation of the smoothed images, contour extraction from the segmented images, shape representation by Fourier descriptors, and contractility assessment. The different stages are variants of mathematically sound and computationally robust algorithms very well established in the image processing community. The physiologic application of the methodology is evaluated by assessing overall contraction in enzymatically dissociated adult rat cardiocytes. Our results demonstrate the effectiveness of the proposed approach in characterizing the true, two-dimensional, “shortening” in the contraction process of adult cardiocytes. We compare the performance of the proposed method to that of a popular edge detection system in the literature. The proposed method not only provides a more comprehensive assessment of the myocyte contraction process but also can potentially eliminate historical concerns and sources of errors caused by myocyte rotation or translation during contraction. Furthermore, the versatility of the image processing techniques makes the method suitable for determining myocyte shortening in cells that usually bend or move during contraction. The proposed method can be utilized to evaluate changes in contractile behavior resulting from drug intervention, disease modeling, transgeneity, or other common applications to mammalian cardiocytes.

Highlights

  • It is estimated that 17.5 million people die of cardiovascular disease (CVD) every year, with an approximate cost of C310.23 billion

  • We propose a complete computational framework-based on well-established image processing techniques for the assessment of contractility of isolated cardiac myocytes

  • The proposed methodology was able to capture a slower recovery period than the rasterline method, which can be attributed to the dimensionality characteristics of both methods. This means that the proposed method is capable of assessing the myocyte’s length, and its overall changes in shape and geometry

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Summary

Introduction

It is estimated that 17.5 million people die of cardiovascular disease (CVD) every year, with an approximate cost of C310.23 billion The study of cardiocyte contractility has helped unveil the fundamental processes underlying heart function in health and disease [1, 2]. The cardiac myocyte is approximately 25 μm in diameter and about 100 μm in length. It is composed of bundles of myofibrils that contain myofilaments. Chemical and physical interactions between the actin and myosin cause the sarcomere length to shorten, allowing the myocyte to contract during the process of excitation-contraction coupling [15]

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