Cytotoxicity is a general term that describes the detrimental effects of substances or environmental changes on cell health. Exposure of cells to a cytotoxic stimulus may compromise metabolic activity, inhibit cell growth or division or ultimately produce cell death. 'Necrotic' cell death is a catastrophic cell lysis. 'Apoptotic' cell death is a more controlled, programmed mechanism. 'Autophagy' is a specialised process whereby cells digest themselves from within. Irrespective of the mechanism of cytotoxicity, once a cell irreversibly loses its membrane integrity it is destined to die.
A number of cytotoxicity assays involve measurement of cell membrane integrity, either with vital dyes that are excluded from healthy cells, e.g. trypan blue or propidium iodide, or via the release of markers from dying cells (e.g. cellular proteases). Metabolic activity measurements, e.g. MTT, LDH or ATP assays are also used to measure cell health and viability. However, despite these methods, few if any involve direct counting of the number of dying cells over time.
The IncuCyte ZOOM® live-cell imaging and analysis system enables real-time, automated cytotoxicity assays within your tissue culture incubator.
The IncuCyte™ Cytotoxicity Assay uses the IncuCyte® Cytotox Reagents to make real time measurements of cell death based on cell membrane integrity, all within your incubator.
When added to the tissue culture growth medium, the IncuCyte® Cytotox Reagents are inert, non-fluorescent and do not enter viable cells. As cells die and membrane integrity is lost, the Cytotox probe enters the cell and fluorescently labels the nuclei. Dying cells are identified and quantified over time by the appearance of green- (or red) labelled nuclei. High definition phase contrast images and movies provide an additional validation of cell death based on morphology (e.g. loss of cytoskeleton structure, loss of motility).
Measure cytotoxicity in tumor, immune or neuronal cultures using the IncuCyte cytotoxicity assay. (Left) Real-time detection of cytotoxicity in HT-1080 fibrosarcoma cells following treatment with the cytotoxic drug camptothecin. Dying cells are labeled green, in real-time, by the mix-and-read IncuCyte® Cytotox Green Reagent. (Right) IncuCyte® Cytotox Red reagent labels dead rat forebrain neurons treated with 333 μM glutamate.
Visualize and validate cytotoxicity with images and movies. Time lapse images of SK-OV-3 ovarian cancer cell death in response to the anti-cancer drug camptothecin. Correlate fluorescent signal from the IncuCyte® Cytotox Reagents with morphological changes associated with cell death. Quantify cytotoxicity using IncuCyte® image analysis tools. User-friendly software enables direct image-based detection of dying cells (pink mask).
Quantify treatment effects automatically and non-invasively. IncuCyte cytotoxicity assay allows every well of a 96/384 well plate to be imaged and analyzed automatically to provide a microplate readout of cytotoxicity over time (left). Time-courses reveal concentration-dependent treatment effects (center). Transform data into concentration-response curves to compare pharmacology (right).
Multiplex cytotoxicity measurements with live-cell counting. Camptothecin (150 nM) treated HT-1080 fibrosarcoma cells (labeled with IncuCyte® NucLight Red Reagent) in the presence of the IncuCyte® Cytotox Green Reagent to detect live/dead cells over time.
Quantify time-courses and concentration-dependence of cytotoxicity and proliferation. Effect of staurosporine on HT1080 cells: (A) Cytotoxicity (B) Cell Count and (C) Concentration-response curves.
Yes, the interaction of cells in complex, tissue-like relationships can be studied in vitro with co-cultures, and cell death can be tracked in those co-cultures with markers of apoptosis and membrane integrity. For the most meaningful data, cell proliferation and cell death can be monitored at the same time in the same culture, with live-cell imaging.
To track a specific cell type throughout the co-culture experiment, start by transducing the cells with one of the NucLight™ reagents, ensuring that it is a different color than the Cytotox reagent used. The cells will grow and associate into dense, interacting cultures, and cell death will be monitored with the Cytotox or Caspase 3/7 reagents.
Note: All dead and dying cells will be positive for the Cytotox or Caspase 3/7 reagent, not just the ones transduced with the NucLight reagent.
The most commonly used method for predicting cell death in cytotoxicity assays is by using a reagent that is impermeant to intact lipid bilayers. Upon the onset of the cell death cascade, the lipid bilayer becomes porous and leaky, allowing the reagent into the cells where it stains the nucleus. Other assays are capable of detecting different stages and forms of cell death. Apoptosis assays detect the presence of certain markers of dying cells, like activated caspases and Annexin V.
View the cytotoxicity assay protocol
Learn more about apoptosis assays
The three assays you mentioned are not mutually exclusive. Cytotoxicity (or cytotox) assays could easily be measured alongside cell proliferation or cell migration assays. The only factors to keep in mind are that you’ll need to have enough imaging channels to monitor the readouts from all of the assays at the same time. For live-cell imaging with the IncuCyte™, that means you could track cell confluence (which needs no fluorochrome), chemotaxis (in either the red or green channel), and cytotoxicity (in the remaining channel).
The range of cytotoxicity assays is very broad, so it’s impossible to provide an answer that applies to all cytotox assay methods. However, for methods that involve a visual-recognition component alongside a fluorescent intensity component, it is possible to differentiate between a number of cells undergoing apoptosis and a single cell lysing. Specific apoptosis assays, when multiplexed, can even provide finer detail, including signalling the onset of the apoptotic cascade or the derangement of the lipid membrane. Assays like ELISAs, where signal is entirely cumulative, could not provide details like these.
A common reason for this problem is continued cell growth throughout the cell death assay, leading to overcrowding in the well. When plating your cells for cytotoxicity assays, make sure to have an exact count, and don’t seed so many cells that your cells will become contact inhibited (by reaching 100% confluence) before your endpoint.
Occasionally, cytotoxic substances can have the paradoxical effect of stimulating cell proliferation at sublethal concentrations. If you routinely see this effect with your combination of cells and cytotoxic agent, this may be the explanation.
IncuCyte™ Cytotox Reagents are fully validated for use with the IncuCyte® System and cytotoxicity assays. Furthermore, they can be combined with our range of IncuCyte™ NucLight™ nuclear labeling reagents, or the IncuCyte™ Caspase 3/7 Reagent for multiplexed measurements of proliferation and apoptosis alongside cytotoxicity in a single well.
|Product||Product Data Sheet||Safety Data Sheet (US)||Qty.||Catalog No.|
|IncuCyte® Cytotox Red Reagent for counting dead cells||5 μL x 5||4632|
|IncuCyte® Cytotox Green Reagent for counting dead cells||5 μL x 5||4633|
|IncuCyte® Caspase 3/7 Reagent for apoptosis||20 μL||4440|
|IncuCyte® Annexin V Red Reagent for apoptosis||100 tests||4641|
|IncuCyte® Annexin V Green Reagent for apoptosis||100 tests||4642|
|IncuCyte® NucLight Red BacMam 3.0 Reagent for nuclear labeling||1 mL||4621|
|IncuCyte® NucLight Green BacMam 3.0 Reagent for nuclear labeling||1 mL||4622|