Background: Analysis of the DNA cell cycle and glutathione content cannot be performed on viable cells, because the fluorescence emissions of the DNA-specific probe Hoechst 33342 and the glutathione-specific probe monobromobimane overlap completely. We decided to explore whether the emissions could
Selection of viable cells with known DNA content
β Scribed by Eugene Hamori; Donna J. Arndt-Jovin; Brian G. Grimwade; Thomas M. Jovin
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 450 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0196-4763
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Cells doubly stained with Hoechst 33342 (Hβ33342) for DNA content and fluorescein diacetate for viability can be selected on the basis of both criteria using a single UV laser flow sorter. The selection is made possible due to resonance energy transfer occurring between the Hβ33342 and fluorescein fluorophores. Both a static fluorescence microscope and a dual laser flow sorter were used to demonstrate that energy transfer occurs in the doubly stained cells and that the sensitized emission in conjunction with the DNA emission can be used to select populations of cells with known DNA content and viability. The results indicate that fluorescein liberated by cellular esterases is freely accessible to the nucleus.
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## Abstract The mean DNA content per cell and heterogeneity of cell populations with respect to DNA content were measured in samples of peripheral blood mononuclear cells from donors of different ages. Nearly all of the cells in these populations are found in the G~1Q~ phase of the cell cycle. Whil