Editing MTT Assay

1. Dissolve MTT in PBS at 2 mg/mL, filtered through 0.22 um polycarbonate membrane filters for sterilization

2. 1 day before assay, seed cells in 96 well (2 X 10^4 cells per well) plates and incubate for one day.

3. Do transfection. At the end of the transfection experiment (4 or 5 hours), replace the transfection mixture&nbsp; with 100 uL of fresh medium, containing 10% FBS.

4. Add twenty-six microliters of 2 mg/mL MTT solution in 1XPBS to each well.

5. Incubate the plates for an additional 4 hr at 37 ºC in a tissue culture incubator.

6. Aspirate off&nbsp; MTT-containing medium.

7. Add 150 uL&nbsp; DMSO to dissolve the formazan crystal formed by living cells, incubate for 1 hr.

8. Read 570 nM

Cell viability (%) = (OD570(sample)/OD570(control)) X 100



Measurement of cell viability and proliferation forms the basis for numerous in vitro assays of a cell population’s response to external factors. The reduction of tetrazolium salts is now widely accepted as a reliable way to examine cell proliferation. The yellow tetrazolium MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide) is reduced by metabolically active cells, in part by the action of dehydrogenase enzymes, to generate reducing equivalents such as NADH and NADPH. The resulting intracellular purple formazan can be solubilized and quantified by spectrophotometric means.

The MTT Cell Proliferation Assay measures the cell proliferation rate and conversely, when metabolic events lead to apoptosis or necrosis, the reduction in cell viability. The number of assay steps has been minimized as much as possible to expedite sample processing. The MTT Reagent yields low background absorbance values in the absence of cells. For each cell type the linear relationship between cell number and signal produced is established, thus allowing an accurate quantification of changes in the rate of cell proliferation.

The MTT Reagent is ready to use and stable at 4°C in the dark for up to eighteen months, provided there is no contamination. Care should be taken not to contaminate the MTT Reagent with cell culture medium during pipetting. We recommend that the appropriate volume required for each experiment be removed and aseptically placed into a separate clean tube and the stock bottle returned to 4°C in the dark. If the MTT Reagent is bluegreen, do not use and refer to the troubleshooting guide on page 6. The Detergent Reagent is supplied ready to use. If the Detergent Reagent has been stored at 4°C, warm the bottle for 5 minutes at 37°C then mix by inverting gently to avoid frothing. The detergent is stable for up to eighteen months at room temperature

1 Plate cells at 1,000 to 100,000 per well.

2 Incubate for 6 to 24 hours.

3 Add 10 μL MTT Reagent.

4 Incubate for 2 to 4 hours until purple precipitate is visible.

5 Add 100 μL Detergent Reagent.

6 Leave at room temperature in the dark for 2 hours.

7 Record absorbance at 570 nm.

1 Harvest suspension cells by centrifugation. Adherent cells should be released from their substrate by trypsinization or scraping.

2 Resuspend cells at 1 x 106 per mL.

3 Prepare serial dilutions of cells in culture medium from

1 x 106 to 1 x 103 cells per mL. 4 Plate out, in triplicate, 100 μL of the dilutions into wells of a microtiter plate.

5 Include three control wells of medium alone to provide the blanks for absorbance readings.

6 Incubate the cells under conditions appropriate for the cell line for 6 to 48 hours (to recover from handling). The time required will vary but 12 hours to overnight is sufficient for most cell types.

7 Add 10 μL of MTT Reagent to each well, including controls.

8 Return plate to cell culture incubator for 2 to 4 hours.

9 Periodically view the cells under an inverted microscope for presence of intracellular punctate purple precipitate.

10 When the purple precipitate is clearly visible under the microscope add 100 μL of Detergent Reagent to all wells, including controls. Swirl gently; do not shake.

11 Leave plate with cover in the dark for 2 to 4 hours or overnight at room temperature.

12 Remove plate cover and measure the absorbance in each well, including the blanks, at 570 nm in a microtiter plate reader. [Absorbances can be read with any filter in the wavelength range of 550 - 600 nm. The reference wavelength should be higher than 650 nm. The blanks should give values close to zero (+/- 0.1).]

13 If the readings are low return the plate to the dark for longer incubation.

14 Determine the average values from triplicate readings and subtract the average value for the blank. Plot absorbance against number of cells/mL. The number of cells to use in your assay should lie within the linear portion of the plot and yield an absorbance of 0.75 - 1.25.

PERFORMING AN ASSAY

The plot of the data obtained in Step 14 on page 3 (absorbance against number of cells) should provide a curve with a linear portion. The optimal number of cells for the assay should fall within the linear portion of the curve and give an absorbance value between 0.75 and 1.25. Then both stimulation and inhibition of cell proliferation can be measured. To run an assay, select an optimal cell number and follow the MTT Cell Proliferation Assay steps 4 to 13 (page 3) using your experimental system, plating in triplicate. Assays will include:

a) Blank wells containing medium only

b) Untreated control cells

c) Test cells treated with the substance to be assayed

If more than 100 μL of medium is used per well, increase the amount of MTT Reagent accordingly; e.g., for 250 μL of medium use 25 μL of MTT Reagent

DATA INTERPRETATION

Absorbance values that are lower than the control cells indicate a reduction in the rate of cell proliferation. Conversely a higher absorbance rate indicates an increase in cell proliferation. Rarely, an increase in proliferation may be offset by cell death; evidence of cell death may be inferred from morphological changes.
[[Category:Protocols]][[Category:Transfection]]