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A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments

BACKGROUND: This paper presents a novel model for proliferating cell populations in labeling experiments. It is especially tailored to the technique of Bromodeoxyuridine (BrdU), which is taken up by dividing cells and thus accumulates with increasing division number during uplabeling. The study of t...

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Detalles Bibliográficos
Autores principales: Schittler, Daniella, Allgöwer, Frank, De Boer, Rob J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750481/
https://www.ncbi.nlm.nih.gov/pubmed/24268033
http://dx.doi.org/10.1186/1752-0509-7-S1-S4
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author Schittler, Daniella
Allgöwer, Frank
De Boer, Rob J
author_facet Schittler, Daniella
Allgöwer, Frank
De Boer, Rob J
author_sort Schittler, Daniella
collection PubMed
description BACKGROUND: This paper presents a novel model for proliferating cell populations in labeling experiments. It is especially tailored to the technique of Bromodeoxyuridine (BrdU), which is taken up by dividing cells and thus accumulates with increasing division number during uplabeling. The study of the evolving label intensities of BrdU labeled cell populations is aimed at quantifying proliferation properties such as division and death rates. RESULTS: In contrast to existing models, our model considers a labeling efficacy that follows a distribution, rather than a uniform value. It thereby allows to account for noise as well as possibly space-dependent heterogeneity in the effective label uptake of the individual cells in a population. Furthermore, it enables more informative comparison with experimental data: The population-level label distribution is provided as a model output, thereby increasing the information content compared to existing models that give the fraction of labeled cells or the mean label intensity. We employ our model to study some naturally arising examples of heterogeneity in label uptake, which are not covered by existing models. With simulations of noisy and spacially heterogeneous label uptake, we demonstrate that our model contributes a more realistic quantitative description of labeling experiments. CONCLUSION: The presented model is to our knowledge the first one that predicts the full label distribution for BrdU labeling experiments. Thus, it can exploit more information, namely the full intensity distribution, from labeling measurements, and thereby opens up new quantitative insights into cell proliferation.
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spelling pubmed-37504812013-08-27 A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments Schittler, Daniella Allgöwer, Frank De Boer, Rob J BMC Syst Biol Research BACKGROUND: This paper presents a novel model for proliferating cell populations in labeling experiments. It is especially tailored to the technique of Bromodeoxyuridine (BrdU), which is taken up by dividing cells and thus accumulates with increasing division number during uplabeling. The study of the evolving label intensities of BrdU labeled cell populations is aimed at quantifying proliferation properties such as division and death rates. RESULTS: In contrast to existing models, our model considers a labeling efficacy that follows a distribution, rather than a uniform value. It thereby allows to account for noise as well as possibly space-dependent heterogeneity in the effective label uptake of the individual cells in a population. Furthermore, it enables more informative comparison with experimental data: The population-level label distribution is provided as a model output, thereby increasing the information content compared to existing models that give the fraction of labeled cells or the mean label intensity. We employ our model to study some naturally arising examples of heterogeneity in label uptake, which are not covered by existing models. With simulations of noisy and spacially heterogeneous label uptake, we demonstrate that our model contributes a more realistic quantitative description of labeling experiments. CONCLUSION: The presented model is to our knowledge the first one that predicts the full label distribution for BrdU labeling experiments. Thus, it can exploit more information, namely the full intensity distribution, from labeling measurements, and thereby opens up new quantitative insights into cell proliferation. BioMed Central 2013-08-12 /pmc/articles/PMC3750481/ /pubmed/24268033 http://dx.doi.org/10.1186/1752-0509-7-S1-S4 Text en Copyright © 2013 Schittler et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Schittler, Daniella
Allgöwer, Frank
De Boer, Rob J
A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments
title A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments
title_full A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments
title_fullStr A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments
title_full_unstemmed A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments
title_short A new model to simulate and analyze proliferating cell populations in BrdU labeling experiments
title_sort new model to simulate and analyze proliferating cell populations in brdu labeling experiments
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750481/
https://www.ncbi.nlm.nih.gov/pubmed/24268033
http://dx.doi.org/10.1186/1752-0509-7-S1-S4
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