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Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept

Bibliographic Details
Main Author: Figueiredo, J
Publication Date: 2018
Other Authors: Rodrigues, I, Ribeiro, J, Fernandes, MS, Melo, S, Sousa, B, Paredes, J, Seruca, R, Sanches, J
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10216/127415
Summary: Immunofluorescence is the gold standard technique to determine the level and spatial distribution of fluorescent-tagged molecules. However, quantitative analysis of fluorescence microscopy images faces crucial challenges such as morphologic variability within cells. In this work, we developed an analytical strategy to deal with cell shape and size variability that is based on an elastic geometric alignment algorithm. Firstly, synthetic images mimicking cell populations with morphological variability were used to test and optimize the algorithm, under controlled conditions. We have computed expression profiles specifically assessing cell-cell interactions (IN profiles) and profiles focusing on the distribution of a marker throughout the intracellular space of single cells (RD profiles). To experimentally validate our analytical pipeline, we have used real images of cell cultures stained for E-cadherin, tubulin and a mitochondria dye, selected as prototypes of membrane, cytoplasmic and organelle-specific markers. The results demonstrated that our algorithm is able to generate a detailed quantitative report and a faithful representation of a large panel of molecules, distributed in distinct cellular compartments, independently of cell's morphological features. This is a simple end-user method that can be widely explored in research and diagnostic labs to unravel protein regulation mechanisms or identify protein expression patterns associated with disease.
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spelling Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical conceptImmunofluorescence is the gold standard technique to determine the level and spatial distribution of fluorescent-tagged molecules. However, quantitative analysis of fluorescence microscopy images faces crucial challenges such as morphologic variability within cells. In this work, we developed an analytical strategy to deal with cell shape and size variability that is based on an elastic geometric alignment algorithm. Firstly, synthetic images mimicking cell populations with morphological variability were used to test and optimize the algorithm, under controlled conditions. We have computed expression profiles specifically assessing cell-cell interactions (IN profiles) and profiles focusing on the distribution of a marker throughout the intracellular space of single cells (RD profiles). To experimentally validate our analytical pipeline, we have used real images of cell cultures stained for E-cadherin, tubulin and a mitochondria dye, selected as prototypes of membrane, cytoplasmic and organelle-specific markers. The results demonstrated that our algorithm is able to generate a detailed quantitative report and a faithful representation of a large panel of molecules, distributed in distinct cellular compartments, independently of cell's morphological features. This is a simple end-user method that can be widely explored in research and diagnostic labs to unravel protein regulation mechanisms or identify protein expression patterns associated with disease.Nature Publishing Group20182018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/127415eng2045-232210.1038/s41598-018-28570-zFigueiredo, JRodrigues, IRibeiro, JFernandes, MSMelo, SSousa, BParedes, JSeruca, RSanches, Jinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-27T18:31:17Zoai:repositorio-aberto.up.pt:10216/127415Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T22:51:08.260609Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
title Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
spellingShingle Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
Figueiredo, J
title_short Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
title_full Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
title_fullStr Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
title_full_unstemmed Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
title_sort Geometric compensation applied to image analysis of cell populations with morphological variability: A new role for a classical concept
author Figueiredo, J
author_facet Figueiredo, J
Rodrigues, I
Ribeiro, J
Fernandes, MS
Melo, S
Sousa, B
Paredes, J
Seruca, R
Sanches, J
author_role author
author2 Rodrigues, I
Ribeiro, J
Fernandes, MS
Melo, S
Sousa, B
Paredes, J
Seruca, R
Sanches, J
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Figueiredo, J
Rodrigues, I
Ribeiro, J
Fernandes, MS
Melo, S
Sousa, B
Paredes, J
Seruca, R
Sanches, J
description Immunofluorescence is the gold standard technique to determine the level and spatial distribution of fluorescent-tagged molecules. However, quantitative analysis of fluorescence microscopy images faces crucial challenges such as morphologic variability within cells. In this work, we developed an analytical strategy to deal with cell shape and size variability that is based on an elastic geometric alignment algorithm. Firstly, synthetic images mimicking cell populations with morphological variability were used to test and optimize the algorithm, under controlled conditions. We have computed expression profiles specifically assessing cell-cell interactions (IN profiles) and profiles focusing on the distribution of a marker throughout the intracellular space of single cells (RD profiles). To experimentally validate our analytical pipeline, we have used real images of cell cultures stained for E-cadherin, tubulin and a mitochondria dye, selected as prototypes of membrane, cytoplasmic and organelle-specific markers. The results demonstrated that our algorithm is able to generate a detailed quantitative report and a faithful representation of a large panel of molecules, distributed in distinct cellular compartments, independently of cell's morphological features. This is a simple end-user method that can be widely explored in research and diagnostic labs to unravel protein regulation mechanisms or identify protein expression patterns associated with disease.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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url https://hdl.handle.net/10216/127415
dc.language.iso.fl_str_mv eng
language eng
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10.1038/s41598-018-28570-z
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