Abstract

Although confocal microscopes have considerably smaller contribution of out-of-focus light than widefield microscopes, the confocal images can still be enhanced mathematically if the optical and data acquisition effects are accounted for. For that, several deconvolution algorithms have been proposed. As a practical solution, maximum-likelihood algorithms with regularization have been used. However, the choice of regularization parameters is often unknown although it has considerable effect on the result of deconvolution process. The aims of this work were: to find good estimates of deconvolution parameters; and to develop an open source software package that would allow testing different deconvolution algorithms and that would be easy to use in practice. Here, Richardson–Lucy algorithm has been implemented together with the total variation regularization in an open source software package IOCBio Microscope. The influence of total variation regularization on deconvolution process is determined by one parameter. We derived a formula to estimate this regularization parameter automatically from the images as the algorithm progresses. To assess the effectiveness of this algorithm, synthetic images were composed on the basis of confocal images of rat cardiomyocytes. From the analysis of deconvolved results, we have determined under which conditions our estimation of total variation regularization parameter gives good results. The estimated total variation regularization parameter can be monitored during deconvolution process and used as a stopping criterion. An inverse relation between the optimal regularization parameter and the peak signal-to-noise ratio of an image is shown. Finally, we demonstrate the use of the developed software by deconvolving images of rat cardiomyocytes with stained mitochondria and sarcolemma obtained by confocal and widefield microscopes.

Highlights

  • In biosciences, fluorescence microscopy is an extremely useful and important method for studying living organisms

  • Deconvolution is a method to reverse the aberrations caused by convolution, that is remove the distortions of the optical train, contributions from out-of-focus objects, and with regularization enabled, reduce the noise originated from detector electronics

  • Where i represents the recorded image stack represented as 3D array, where each item value corresponds to the intensity of a measured voxel, o is the object, h is the point spread function (PSF) defined by the optical train of a specific microscope, ⊗ denotes convolution operation, P represents Poisson noise originating from counting photons

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Summary

Introduction

Fluorescence microscopy is an extremely useful and important method for studying living organisms. Confocal microscopy has several advantages over traditional widefield microscopy. Despite the advantages over widefield microscopy, confocal images contain imperfections, for example, aberrations due to nonideal optical pathway, residual out-of-focus light, noise from detector electronics, etc. In this paper we focus on image enhancement of microscope images by deconvolution (Cannell et al, 2006). Deconvolution is a method to reverse the aberrations caused by convolution, that is remove the distortions of the optical train, contributions from out-of-focus objects, and with regularization enabled, reduce the noise originated from detector electronics. It is a method that can efficiently enhance both widefield microscopy and confocal microscopy images. It can considerably improve image contrast and reduce noise in microscope images

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