IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0181941.html
   My bibliography  Save this article

A computational modelling framework to quantify the effects of passaging cell lines

Author

Listed:
  • Wang Jin
  • Catherine J Penington
  • Scott W McCue
  • Matthew J Simpson

Abstract

In vitro cell culture is routinely used to grow and supply a sufficiently large number of cells for various types of cell biology experiments. Previous experimental studies report that cell characteristics evolve as the passage number increases, and various cell lines can behave differently at high passage numbers. To provide insight into the putative mechanisms that might give rise to these differences, we perform in silico experiments using a random walk model to mimic the in vitro cell culture process. Our results show that it is possible for the average proliferation rate to either increase or decrease as the passaging process takes place, and this is due to a competition between the initial heterogeneity and the degree to which passaging damages the cells. We also simulate a suite of scratch assays with cells from near–homogeneous and heterogeneous cell lines, at both high and low passage numbers. Although it is common in the literature to report experimental results without disclosing the passage number, our results show that we obtain significantly different closure rates when performing in silico scratch assays using cells with different passage numbers. Therefore, we suggest that the passage number should always be reported to ensure that the experiment is as reproducible as possible. Furthermore, our modelling also suggests some avenues for further experimental examination that could be used to validate or refine our simulation results.

Suggested Citation

  • Wang Jin & Catherine J Penington & Scott W McCue & Matthew J Simpson, 2017. "A computational modelling framework to quantify the effects of passaging cell lines," PLOS ONE, Public Library of Science, vol. 12(7), pages 1-16, July.
  • Handle: RePEc:plo:pone00:0181941
    DOI: 10.1371/journal.pone.0181941
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0181941
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0181941&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0181941?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Katrina K Treloar & Matthew J Simpson, 2013. "Sensitivity of Edge Detection Methods for Quantifying Cell Migration Assays," PLOS ONE, Public Library of Science, vol. 8(6), pages 1-10, June.
    2. Simpson, Matthew J. & Landman, Kerry A. & Hughes, Barry D., 2010. "Cell invasion with proliferation mechanisms motivated by time-lapse data," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 389(18), pages 3779-3790.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Matthew J Simpson & Parvathi Haridas & D L Sean McElwain, 2014. "Do Pioneer Cells Exist?," PLOS ONE, Public Library of Science, vol. 9(1), pages 1-11, January.
    2. Baker, Ruth E. & Simpson, Matthew J., 2012. "Models of collective cell motion for cell populations with different aspect ratio: Diffusion, proliferation and travelling waves," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 391(14), pages 3729-3750.
    3. Katrina K Treloar & Matthew J Simpson, 2013. "Sensitivity of Edge Detection Methods for Quantifying Cell Migration Assays," PLOS ONE, Public Library of Science, vol. 8(6), pages 1-10, June.
    4. Brenda N Vo & Christopher C Drovandi & Anthony N Pettitt & Graeme J Pettet, 2015. "Melanoma Cell Colony Expansion Parameters Revealed by Approximate Bayesian Computation," PLOS Computational Biology, Public Library of Science, vol. 11(12), pages 1-22, December.
    5. Irons, Carolyn & Plank, Michael J. & Simpson, Matthew J., 2016. "Lattice-free models of directed cell motility," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 442(C), pages 110-121.
    6. Clements, Alastair J. & Fadai, Nabil T., 2022. "Agent-based modelling of sports riots," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 597(C).

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0181941. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.