Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Improved method for computing potential doubling time from flow cytometric data.

R A White1, N H Terry, M L Meistrich

  • 1Department of Biomathematics, University of Texas M.D. Anderson Cancer Center, Houston 77030.

Cytometry
|January 1, 1990
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Spermatogonial asynchrony in Tex14 mutant mice lacking intercellular bridges.

Reproduction (Cambridge, England)·2020
Same author

Effect of hormone modulations on donor-derived spermatogenesis or colonization after syngeneic and xenotransplantation in mice.

Andrology·2018
Same author

Leydig cells contribute to the inhibition of spermatogonial differentiation after irradiation of the rat.

Andrology·2016
Same author

Increasing testicular temperature by exposure to elevated ambient temperatures restores spermatogenesis in adult Utp14b (jsd) mutant (jsd) mice.

Andrology·2014
Same author

Dynamic Hedgehog signalling pathway activity in germline stem cells.

Andrology·2014
Same author

Hormone suppression with GnRH antagonist promotes spermatogenic recovery from transplanted spermatogonial stem cells in irradiated cynomolgus monkeys.

Andrology·2013

This study introduces a new method to calculate the potential doubling time (Tpot) of cells using relative movement analysis. This approach extends existing techniques for measuring DNA synthesis duration (Ts), offering a more comprehensive cell proliferation assessment.

Area of Science:

  • Cell Biology
  • Biophysics
  • Quantitative Biology

Background:

  • Relative movement methods analyze DNA and antibody-labeled cell fluorescence over time.
  • These methods are established for calculating DNA synthesis duration (Ts).
  • Extending these methods can provide further insights into cell population dynamics.

Purpose of the Study:

  • To extend relative movement methods for calculating potential doubling time (Tpot).
  • To enable Tpot calculation in cell populations with quiescent cells and no cell loss.
  • To provide a direct method for determining Tpot from existing flow cytometry data.

Main Methods:

  • Utilized bivariate flow cytometry to analyze cells labeled with bromodeoxyuridine.
  • Extended relative movement calculations to incorporate quiescent and non-proliferating cells.

Related Experiment Videos

  • Introduced a new quantity 'v' derived from labeled divided and undivided cell fractions.
  • Main Results:

    • Demonstrated that the quantity 'v' is time-independent.
    • Established the relationship v = ln(2)Ts/Tpot.
    • Showed that Tpot can be directly calculated as Tpot = ln(2)Ts/v.

    Conclusions:

    • The extended relative movement method accurately computes potential doubling time (Tpot).
    • This method simplifies Tpot determination using standard flow cytometry data.
    • The utility was validated using Chinese hamster ovary cells.