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A transfer function approach to measuring cell inheritance

BACKGROUND: The inheritance of cellular material between parent and daughter cells during mitosis is highly influential in defining the properties of the cell and therefore the population lineage. This is of particular relevance when studying cell population evolution to assess the impact of a disea...

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Autores principales: Rees, Paul, Brown, M Rowan, Summers, Huw D, Holton, Mark D, Errington, Rachel J, Chappell, Sally C, Smith, Paul J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056740/
https://www.ncbi.nlm.nih.gov/pubmed/21342507
http://dx.doi.org/10.1186/1752-0509-5-31
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author Rees, Paul
Brown, M Rowan
Summers, Huw D
Holton, Mark D
Errington, Rachel J
Chappell, Sally C
Smith, Paul J
author_facet Rees, Paul
Brown, M Rowan
Summers, Huw D
Holton, Mark D
Errington, Rachel J
Chappell, Sally C
Smith, Paul J
author_sort Rees, Paul
collection PubMed
description BACKGROUND: The inheritance of cellular material between parent and daughter cells during mitosis is highly influential in defining the properties of the cell and therefore the population lineage. This is of particular relevance when studying cell population evolution to assess the impact of a disease or the perturbation due to a drug treatment. The usual technique to investigate inheritance is to use time-lapse microscopy with an appropriate biological marker, however, this is time consuming and the number of inheritance events captured are too low to be statistically meaningful. RESULTS: Here we demonstrate the use of a high throughput fluorescence measurement technique e.g. flow cytometry, to measure the fluorescence from quantum dot markers which can be used to target particular cellular sites. By relating, the fluorescence intensity measured between two time intervals to a transfer function we are able to deconvolve the inheritance of cellular material during mitosis. To demonstrate our methodology we use CdTe/ZnS quantum dots to measure the ratio of endosomes inherited by the two daughter cells during mitosis in the U2-OS, human osteoscarcoma cell line. The ratio determined is in excellent agreement with results obtained previously using a more complex and computational intensive bespoke stochastic model. CONCLUSIONS: The use of a transfer function approach allows us to utilise high throughput measurement of large cell populations to derive statistically relevant measurements of the inheritance of cellular material. This approach can be used to measure the inheritance of organelles, proteins etc. and also particles introduced to cells for drug delivery.
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spelling pubmed-30567402011-03-31 A transfer function approach to measuring cell inheritance Rees, Paul Brown, M Rowan Summers, Huw D Holton, Mark D Errington, Rachel J Chappell, Sally C Smith, Paul J BMC Syst Biol Methodology Article BACKGROUND: The inheritance of cellular material between parent and daughter cells during mitosis is highly influential in defining the properties of the cell and therefore the population lineage. This is of particular relevance when studying cell population evolution to assess the impact of a disease or the perturbation due to a drug treatment. The usual technique to investigate inheritance is to use time-lapse microscopy with an appropriate biological marker, however, this is time consuming and the number of inheritance events captured are too low to be statistically meaningful. RESULTS: Here we demonstrate the use of a high throughput fluorescence measurement technique e.g. flow cytometry, to measure the fluorescence from quantum dot markers which can be used to target particular cellular sites. By relating, the fluorescence intensity measured between two time intervals to a transfer function we are able to deconvolve the inheritance of cellular material during mitosis. To demonstrate our methodology we use CdTe/ZnS quantum dots to measure the ratio of endosomes inherited by the two daughter cells during mitosis in the U2-OS, human osteoscarcoma cell line. The ratio determined is in excellent agreement with results obtained previously using a more complex and computational intensive bespoke stochastic model. CONCLUSIONS: The use of a transfer function approach allows us to utilise high throughput measurement of large cell populations to derive statistically relevant measurements of the inheritance of cellular material. This approach can be used to measure the inheritance of organelles, proteins etc. and also particles introduced to cells for drug delivery. BioMed Central 2011-02-22 /pmc/articles/PMC3056740/ /pubmed/21342507 http://dx.doi.org/10.1186/1752-0509-5-31 Text en Copyright ©2011 Rees 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 Methodology Article
Rees, Paul
Brown, M Rowan
Summers, Huw D
Holton, Mark D
Errington, Rachel J
Chappell, Sally C
Smith, Paul J
A transfer function approach to measuring cell inheritance
title A transfer function approach to measuring cell inheritance
title_full A transfer function approach to measuring cell inheritance
title_fullStr A transfer function approach to measuring cell inheritance
title_full_unstemmed A transfer function approach to measuring cell inheritance
title_short A transfer function approach to measuring cell inheritance
title_sort transfer function approach to measuring cell inheritance
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056740/
https://www.ncbi.nlm.nih.gov/pubmed/21342507
http://dx.doi.org/10.1186/1752-0509-5-31
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