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Determination of lymphocyte division by flow cytometry
1Division of Cell Biology, John Curtin School of Medical Research, Australian National University, Canberra.
Journal of Immunological Methods
|May 2, 1994
Summary
This study introduces a novel fluorescent labeling method to track individual cell division history. The technique allows for the resolution of multiple cell generations using flow cytometry.
Area of Science:
- Cell Biology
- Immunology
- Biotechnology
Background:
- Current cell division tracking methods are limited, offering only single or few division insights.
- Existing methods quantify overall cell division but lack individual cell history resolution.
Purpose of the Study:
- To develop a new technique for tracking multiple successive cell divisions in individual cells.
- To enable immunophenotyping of dividing cells alongside division history analysis.
Main Methods:
- Utilizing an intracellular, fluorescein-derived fluorescent label that is equally divided between daughter cells.
- Applying the technique to both in vitro cell cultures and in vivo adoptively transferred cells.
- Employing flow cytometry for the resolution of multiple cell generations.
Main Results:
- The new method successfully resolves multiple successive cell generations.
- The technique allows for the simultaneous immunophenotyping of dividing cells using compatible fluorochromes.
- Demonstrated applicability in both in vitro and in vivo settings.
Conclusions:
- This novel technique provides a powerful tool for detailed analysis of cell division history.
- It overcomes limitations of existing methods by enabling tracking of individual cell lineages over multiple generations.
- The method facilitates combined analysis of cell proliferation and immunophenotype.