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A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks

BACKGROUND: Modeling of cellular functions on the basis of experimental observation is increasingly common in the field of cellular signaling. However, such modeling requires a large amount of quantitative data of signaling events with high spatio-temporal resolution. A novel technique which allows...

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Autores principales: Ozaki, Yu-ichi, Uda, Shinsuke, Saito, Takeshi H., Chung, Jaehoon, Kubota, Hiroyuki, Kuroda, Shinya
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848603/
https://www.ncbi.nlm.nih.gov/pubmed/20376360
http://dx.doi.org/10.1371/journal.pone.0009955
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author Ozaki, Yu-ichi
Uda, Shinsuke
Saito, Takeshi H.
Chung, Jaehoon
Kubota, Hiroyuki
Kuroda, Shinya
author_facet Ozaki, Yu-ichi
Uda, Shinsuke
Saito, Takeshi H.
Chung, Jaehoon
Kubota, Hiroyuki
Kuroda, Shinya
author_sort Ozaki, Yu-ichi
collection PubMed
description BACKGROUND: Modeling of cellular functions on the basis of experimental observation is increasingly common in the field of cellular signaling. However, such modeling requires a large amount of quantitative data of signaling events with high spatio-temporal resolution. A novel technique which allows us to obtain such data is needed for systems biology of cellular signaling. METHODOLOGY/PRINCIPAL FINDINGS: We developed a fully automatable assay technique, termed quantitative image cytometry (QIC), which integrates a quantitative immunostaining technique and a high precision image-processing algorithm for cell identification. With the aid of an automated sample preparation system, this device can quantify protein expression, phosphorylation and localization with subcellular resolution at one-minute intervals. The signaling activities quantified by the assay system showed good correlation with, as well as comparable reproducibility to, western blot analysis. Taking advantage of the high spatio-temporal resolution, we investigated the signaling dynamics of the ERK pathway in PC12 cells. CONCLUSIONS/SIGNIFICANCE: The QIC technique appears as a highly quantitative and versatile technique, which can be a convenient replacement for the most conventional techniques including western blot, flow cytometry and live cell imaging. Thus, the QIC technique can be a powerful tool for investigating the systems biology of cellular signaling.
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spelling pubmed-28486032010-04-07 A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks Ozaki, Yu-ichi Uda, Shinsuke Saito, Takeshi H. Chung, Jaehoon Kubota, Hiroyuki Kuroda, Shinya PLoS One Research Article BACKGROUND: Modeling of cellular functions on the basis of experimental observation is increasingly common in the field of cellular signaling. However, such modeling requires a large amount of quantitative data of signaling events with high spatio-temporal resolution. A novel technique which allows us to obtain such data is needed for systems biology of cellular signaling. METHODOLOGY/PRINCIPAL FINDINGS: We developed a fully automatable assay technique, termed quantitative image cytometry (QIC), which integrates a quantitative immunostaining technique and a high precision image-processing algorithm for cell identification. With the aid of an automated sample preparation system, this device can quantify protein expression, phosphorylation and localization with subcellular resolution at one-minute intervals. The signaling activities quantified by the assay system showed good correlation with, as well as comparable reproducibility to, western blot analysis. Taking advantage of the high spatio-temporal resolution, we investigated the signaling dynamics of the ERK pathway in PC12 cells. CONCLUSIONS/SIGNIFICANCE: The QIC technique appears as a highly quantitative and versatile technique, which can be a convenient replacement for the most conventional techniques including western blot, flow cytometry and live cell imaging. Thus, the QIC technique can be a powerful tool for investigating the systems biology of cellular signaling. Public Library of Science 2010-04-01 /pmc/articles/PMC2848603/ /pubmed/20376360 http://dx.doi.org/10.1371/journal.pone.0009955 Text en Ozaki et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ozaki, Yu-ichi
Uda, Shinsuke
Saito, Takeshi H.
Chung, Jaehoon
Kubota, Hiroyuki
Kuroda, Shinya
A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks
title A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks
title_full A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks
title_fullStr A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks
title_full_unstemmed A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks
title_short A Quantitative Image Cytometry Technique for Time Series or Population Analyses of Signaling Networks
title_sort quantitative image cytometry technique for time series or population analyses of signaling networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848603/
https://www.ncbi.nlm.nih.gov/pubmed/20376360
http://dx.doi.org/10.1371/journal.pone.0009955
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