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Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data
BACKGROUND: With the advent of new high-throughput electron microscopy techniques such as serial block-face scanning electron microscopy (SBF-SEM) and focused ion-beam scanning electron microscopy (FIB-SEM) biomedical scientists can study sub-cellular structural mechanisms of heart disease at high r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921388/ https://www.ncbi.nlm.nih.gov/pubmed/31856827 http://dx.doi.org/10.1186/s12911-019-0962-1 |
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author | Khadangi, Afshin Hanssen, Eric Rajagopal, Vijay |
author_facet | Khadangi, Afshin Hanssen, Eric Rajagopal, Vijay |
author_sort | Khadangi, Afshin |
collection | PubMed |
description | BACKGROUND: With the advent of new high-throughput electron microscopy techniques such as serial block-face scanning electron microscopy (SBF-SEM) and focused ion-beam scanning electron microscopy (FIB-SEM) biomedical scientists can study sub-cellular structural mechanisms of heart disease at high resolution and high volume. Among several key components that determine healthy contractile function in cardiomyocytes are Z-disks or Z-lines, which are located at the lateral borders of the sarcomere, the fundamental unit of striated muscle. Z-disks play the important role of anchoring contractile proteins within the cell that make the heartbeat. Changes to their organization can affect the force with which the cardiomyocyte contracts and may also affect signaling pathways that regulate cardiomyocyte health and function. Compared to other components in the cell, such as mitochondria, Z-disks appear as very thin linear structures in microscopy data with limited difference in contrast to the remaining components of the cell. METHODS: In this paper, we propose to generate a 3D model of Z-disks within single adult cardiac cells from an automated segmentation of a large serial-block-face scanning electron microscopy (SBF-SEM) dataset. The proposed fully automated segmentation scheme is comprised of three main modules including “pre-processing”, “segmentation” and “refinement”. We represent a simple, yet effective model to perform segmentation and refinement steps. Contrast stretching, and Gaussian kernels are used to pre-process the dataset, and well-known “Sobel operators” are used in the segmentation module. RESULTS: We have validated our model by comparing segmentation results with ground-truth annotated Z-disks in terms of pixel-wise accuracy. The results show that our model correctly detects Z-disks with 90.56% accuracy. We also compare and contrast the accuracy of the proposed algorithm in segmenting a FIB-SEM dataset against the accuracy of segmentations from a machine learning program called Ilastik and discuss the advantages and disadvantages that these two approaches have. CONCLUSIONS: Our validation results demonstrate the robustness and reliability of our algorithm and model both in terms of validation metrics and in terms of a comparison with a 3D visualisation of Z-disks obtained using immunofluorescence based confocal imaging. |
format | Online Article Text |
id | pubmed-6921388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69213882019-12-30 Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data Khadangi, Afshin Hanssen, Eric Rajagopal, Vijay BMC Med Inform Decis Mak Research BACKGROUND: With the advent of new high-throughput electron microscopy techniques such as serial block-face scanning electron microscopy (SBF-SEM) and focused ion-beam scanning electron microscopy (FIB-SEM) biomedical scientists can study sub-cellular structural mechanisms of heart disease at high resolution and high volume. Among several key components that determine healthy contractile function in cardiomyocytes are Z-disks or Z-lines, which are located at the lateral borders of the sarcomere, the fundamental unit of striated muscle. Z-disks play the important role of anchoring contractile proteins within the cell that make the heartbeat. Changes to their organization can affect the force with which the cardiomyocyte contracts and may also affect signaling pathways that regulate cardiomyocyte health and function. Compared to other components in the cell, such as mitochondria, Z-disks appear as very thin linear structures in microscopy data with limited difference in contrast to the remaining components of the cell. METHODS: In this paper, we propose to generate a 3D model of Z-disks within single adult cardiac cells from an automated segmentation of a large serial-block-face scanning electron microscopy (SBF-SEM) dataset. The proposed fully automated segmentation scheme is comprised of three main modules including “pre-processing”, “segmentation” and “refinement”. We represent a simple, yet effective model to perform segmentation and refinement steps. Contrast stretching, and Gaussian kernels are used to pre-process the dataset, and well-known “Sobel operators” are used in the segmentation module. RESULTS: We have validated our model by comparing segmentation results with ground-truth annotated Z-disks in terms of pixel-wise accuracy. The results show that our model correctly detects Z-disks with 90.56% accuracy. We also compare and contrast the accuracy of the proposed algorithm in segmenting a FIB-SEM dataset against the accuracy of segmentations from a machine learning program called Ilastik and discuss the advantages and disadvantages that these two approaches have. CONCLUSIONS: Our validation results demonstrate the robustness and reliability of our algorithm and model both in terms of validation metrics and in terms of a comparison with a 3D visualisation of Z-disks obtained using immunofluorescence based confocal imaging. BioMed Central 2019-12-19 /pmc/articles/PMC6921388/ /pubmed/31856827 http://dx.doi.org/10.1186/s12911-019-0962-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Khadangi, Afshin Hanssen, Eric Rajagopal, Vijay Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data |
title | Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data |
title_full | Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data |
title_fullStr | Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data |
title_full_unstemmed | Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data |
title_short | Automated segmentation of cardiomyocyte Z-disks from high-throughput scanning electron microscopy data |
title_sort | automated segmentation of cardiomyocyte z-disks from high-throughput scanning electron microscopy data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921388/ https://www.ncbi.nlm.nih.gov/pubmed/31856827 http://dx.doi.org/10.1186/s12911-019-0962-1 |
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