Apoptosis Assays Flashcards
Sucrose Velocity Sedimentation
Dose Range
Ssb > 5 Gy
Dsb > 15 Gy
Technique
Larger DNA fragments sediment to a greater extent
Limitations
Insensitive to clinically-relevant low radiation doses
Filter Elution
Dose Range
Ssb > 1 Gy (alkaline elution)
Dsb > 5 Gy (Neutral elution)
Technique
Smaller DNA fragments elute more quickly through a filter of defined pore size
Limitations
Uncertain which DNA lesions are being detected
Nucleoid sedimentation
Dose Range
Ssb 1-20 Gy
Technique
Irradiatied cells show altered DNA supercoiling within nucleus
Limitations
Uncertain which DNA lesions are being detected
Pulse-field gel electrophoresis (PFGE)
Dose Range
Dsb > 5-10 Gy
Technique
Allows for resolution of DNA-dsb, which can be quantified by relative migration within the gel
Limitations
Uncertain effects of DNA conformation. High number of cells in S phase may bias results of assay
Comet Assay
Dose Range
Ssb >1 Gy (alkaline lysis)
Dsb > 2 Gy (neutral lysis)
Technique
Following lysis, individual nuclei are subjected to agarose gel electrophoresis. The DNA that moves out of the nucleus (head) to form the “gail” of the comet is quantified to provide a measure of DNA damage
Limitations
Requires image analysis system to quantify DNA damage. Increased numbers of cells in S phase may bias assay
Fluorescence in situ hybridization (FISH)
Dose Range
Doses > 1 Gy
Technique
Chromosome-specific probes, which can be detected with a fluorescent ligand, are used to identify radiation-incuced translocations
Limitations
May be difficult to interpret in tumor cells that contain translocations prior to irradiation
Premature chromosome condensation (PCC)
Dose Range
Doses > 1 Gy
Technique
An irradiated interpose cell is fused to a mitotic cell. The chromosomes in the interphase cell undergo premature condensation, allowing radiation-induced chromosome damage to be scored
Limitations
May be difficult to interpret in tumor cells that contain chromosome aberrations prior to irradiation
gamma-H2AX intranuclear foci
Dose Range
Doses > 0.05 Gy
Technique
Immunofluorescence microscopy or flow cytometry using an antibody to gamma-H2AX phosphoprotein
Limitations
Requires image analysis system. No standard for size of type of foci to count as DNA breaks