Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images

Abstract Background Cell-scaffold contact measurements are derived from pairs of co-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of stained cells and three types of scaffolds (i.e., spun coat, large microfiber, and medium microfiber). Our analysis of...

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Main Authors: Peter Bajcsy, Soweon Yoon, Stephen J. Florczyk, Nathan A. Hotaling, Mylene Simon, Piotr M. Szczypinski, Nicholas J. Schaub, Carl G. Simon, Mary Brady, Ram D. Sriram
Format: Article
Language:English
Published: BMC 2017-11-01
Series:BMC Bioinformatics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12859-017-1928-x
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spelling doaj-ad192240447c4879b02b94b2cf098b2e2020-11-24T23:05:51ZengBMCBMC Bioinformatics1471-21052017-11-0118112310.1186/s12859-017-1928-xModeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized imagesPeter Bajcsy0Soweon Yoon1Stephen J. Florczyk2Nathan A. Hotaling3Mylene Simon4Piotr M. Szczypinski5Nicholas J. Schaub6Carl G. Simon7Mary Brady8Ram D. Sriram9Information Technology Laboratory, National Institute of Standards and TechnologyInformation Technology Laboratory, National Institute of Standards and TechnologyMaterial Measurement Laboratory, National Institute of Standards and TechnologyNational Eye Institute, National Institute of HealthInformation Technology Laboratory, National Institute of Standards and TechnologyLodz University of TechnologyMaterial Measurement Laboratory, National Institute of Standards and TechnologyMaterial Measurement Laboratory, National Institute of Standards and TechnologyInformation Technology Laboratory, National Institute of Standards and TechnologyInformation Technology Laboratory, National Institute of Standards and TechnologyAbstract Background Cell-scaffold contact measurements are derived from pairs of co-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of stained cells and three types of scaffolds (i.e., spun coat, large microfiber, and medium microfiber). Our analysis of the acquired terabyte-sized collection is motivated by the need to understand the nature of the shape dimensionality (1D vs 2D vs 3D) of cell-scaffold interactions relevant to tissue engineers that grow cells on biomaterial scaffolds. Results We designed five statistical and three geometrical contact models, and then down-selected them to one from each category using a validation approach based on physically orthogonal measurements to CLSM. The two selected models were applied to 414 z-stacks with three scaffold types and all contact results were visually verified. A planar geometrical model for the spun coat scaffold type was validated from atomic force microscopy images by computing surface roughness of 52.35 nm ±31.76 nm which was 2 to 8 times smaller than the CLSM resolution. A cylindrical model for fiber scaffolds was validated from multi-view 2D scanning electron microscopy (SEM) images. The fiber scaffold segmentation error was assessed by comparing fiber diameters from SEM and CLSM to be between 0.46% to 3.8% of the SEM reference values. For contact verification, we constructed a web-based visual verification system with 414 pairs of images with cells and their segmentation results, and with 4968 movies with animated cell, scaffold, and contact overlays. Based on visual verification by three experts, we report the accuracy of cell segmentation to be 96.4% with 94.3% precision, and the accuracy of cell-scaffold contact for a statistical model to be 62.6% with 76.7% precision and for a geometrical model to be 93.5% with 87.6% precision. Conclusions The novelty of our approach lies in (1) representing cell-scaffold contact sites with statistical intensity and geometrical shape models, (2) designing a methodology for validating 3D geometrical contact models and (3) devising a mechanism for visual verification of hundreds of 3D measurements. The raw and processed data are publicly available from https://isg.nist.gov/deepzoomweb/data/ together with the web -based verification system.http://link.springer.com/article/10.1186/s12859-017-1928-xCo-localizationCellular measurementsCell-scaffold contactSegmentation modelsContact evaluationWeb-based verification
collection DOAJ
language English
format Article
sources DOAJ
author Peter Bajcsy
Soweon Yoon
Stephen J. Florczyk
Nathan A. Hotaling
Mylene Simon
Piotr M. Szczypinski
Nicholas J. Schaub
Carl G. Simon
Mary Brady
Ram D. Sriram
spellingShingle Peter Bajcsy
Soweon Yoon
Stephen J. Florczyk
Nathan A. Hotaling
Mylene Simon
Piotr M. Szczypinski
Nicholas J. Schaub
Carl G. Simon
Mary Brady
Ram D. Sriram
Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images
BMC Bioinformatics
Co-localization
Cellular measurements
Cell-scaffold contact
Segmentation models
Contact evaluation
Web-based verification
author_facet Peter Bajcsy
Soweon Yoon
Stephen J. Florczyk
Nathan A. Hotaling
Mylene Simon
Piotr M. Szczypinski
Nicholas J. Schaub
Carl G. Simon
Mary Brady
Ram D. Sriram
author_sort Peter Bajcsy
title Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images
title_short Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images
title_full Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images
title_fullStr Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images
title_full_unstemmed Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images
title_sort modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2017-11-01
description Abstract Background Cell-scaffold contact measurements are derived from pairs of co-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of stained cells and three types of scaffolds (i.e., spun coat, large microfiber, and medium microfiber). Our analysis of the acquired terabyte-sized collection is motivated by the need to understand the nature of the shape dimensionality (1D vs 2D vs 3D) of cell-scaffold interactions relevant to tissue engineers that grow cells on biomaterial scaffolds. Results We designed five statistical and three geometrical contact models, and then down-selected them to one from each category using a validation approach based on physically orthogonal measurements to CLSM. The two selected models were applied to 414 z-stacks with three scaffold types and all contact results were visually verified. A planar geometrical model for the spun coat scaffold type was validated from atomic force microscopy images by computing surface roughness of 52.35 nm ±31.76 nm which was 2 to 8 times smaller than the CLSM resolution. A cylindrical model for fiber scaffolds was validated from multi-view 2D scanning electron microscopy (SEM) images. The fiber scaffold segmentation error was assessed by comparing fiber diameters from SEM and CLSM to be between 0.46% to 3.8% of the SEM reference values. For contact verification, we constructed a web-based visual verification system with 414 pairs of images with cells and their segmentation results, and with 4968 movies with animated cell, scaffold, and contact overlays. Based on visual verification by three experts, we report the accuracy of cell segmentation to be 96.4% with 94.3% precision, and the accuracy of cell-scaffold contact for a statistical model to be 62.6% with 76.7% precision and for a geometrical model to be 93.5% with 87.6% precision. Conclusions The novelty of our approach lies in (1) representing cell-scaffold contact sites with statistical intensity and geometrical shape models, (2) designing a methodology for validating 3D geometrical contact models and (3) devising a mechanism for visual verification of hundreds of 3D measurements. The raw and processed data are publicly available from https://isg.nist.gov/deepzoomweb/data/ together with the web -based verification system.
topic Co-localization
Cellular measurements
Cell-scaffold contact
Segmentation models
Contact evaluation
Web-based verification
url http://link.springer.com/article/10.1186/s12859-017-1928-x
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