𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Estimating cell death in G2M using bivariate BrdUrd/DNA flow cytometry

✍ Scribed by R. Allen White; David M. Asmuth; Ying Lu; Nan Wang; Xiao-Dong Li; Lisa Reece; Richard B. Pollard; Mostafa Nokta; James F. Leary; Nicholas H. A. Terry


Book ID
102137924
Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
188 KB
Volume
66A
Category
Article
ISSN
0196-4763

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Background

In an accompanying paper (Asmuth et al.) it was found necessary to include cell death explicitly to estimate parameters of cell proliferation. The use of bivariate flow cytometry to estimate the phase durations and the doubling times of cells labeled with thymidine analogues is well established. However, these methods of analysis do not consider the possibility of cell death. This report demonstrates that estimating cell death in G~2~/M is possible.

Methods

Mathematical models for the experimental quantities, the fraction of labeled undivided cells, the fraction of labeled divided cells, and the relative movement were developed. These models include the possibility that, of the cells with G~2~/M DNA content, only a certain fraction will divide, with the remainder dying after some time T~R~. Simulation studies were conducted to test the possibility of using simple methods to estimate phase durations and cell death rates.

Results

Cell death alters the estimates of phase transit times in a rather complex manner that depends on the lifetime of the doomed cells. However, it is still possible to obtain estimates of the phase durations of cells in S and G~2~/M and the death rates of cells in G~2~/M.

Conclusions

The methods presented herein provide a new way to characterize cell populations that includes cell death rates and common measurements of cell proliferation. Β© 2005 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Estimation of kinetic cell-cycle-related
✍ James W. Jacobberger; R. Michael Sramkoski; Susan B. Wormsley; Wade E. Bolton πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 170 KB πŸ‘ 1 views

Background: Flow cytometry of immunofluorescence and DNA content provides measures of cell-cycle-related gene expression (protein and/or epitope levels) for asynchronously growing cells. From these data, time-related expression through S phase can be directly measured. However, for G1, G2, and M pha

Flow cytometric analysis of G1- and G2/M
✍ Michael NΓΌsse; Wolfgang Beisker; Christine Hoffmann; Attila Tarnok πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 790 KB

## Abstract Several subcompartments of the cell cycle in addition to the G~1~‐, S‐, and G~2~‐phases usually observed were identified by simultaneous flow cytometric measurements of ethidium bromide fluorescence and side scatter intensity of cell nuclei. Metaphase cells and very early G~1~‐phase cel