Measuring Viability in GFP Expressing Cells With the Tali® Image Cytometer

The Tali® Image Cytometer is a valuable tool for routine cell analysis, delivering quantitative data unavailable from a quick microscope check. In addition, the Tali® cytometer allows accurate analysis for many of the routine cell health and vitality protocols that are cumbersome and time consuming by flow cytometry. The instrument also provides researchers with a rapid, convenient tool for routine two-color analysis that can be used in place of flow cytometry or as a pre-run verification. With a small footprint, the Tali® Image Cytometer performs several common assays right at the benchtop.

In this application note, we demonstrate that the Tali® cytometer delivers accurate cell counting and GFP fluorescence data for four BacMam transduced cell lines. Actual cell counts, calculated concentration, and population percentage are reported for GFP expression and viability of the sample. These data are in concordance with the results obtained using flow cytometry.

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Materials and Methods

The Tali® Image Cytometer is capable of measuring cellular fluorescence that falls within the two fluorescence channels of the instrument: (1) 458 nm excitation with a 525/20 nm emission filter (green channel) and (2) 530 nm excitation with a 585 nm longpass emission filter (red channel). To accurately assess the viability of GFP-expressing cells, the fluorescent dye in the Tali® Viability Kit–Dead Cell Red was matched to the red channel in the Tali® instrument. The assay, optimized for a streamlined workflow, uses minimal cell sample and reagent and can be performed in cell growth medium typically in less than five minutes.

U2OS, 293MSR, HEKn, and CHO-S cells were transduced using a nucleartargeted GFP BacMam 2.0 expression construct (CellLight® Nucleus-GFP). Briefly, 7.5 x 105 cells were added to a T75 flask along with 0.5 mL of prepared BacMam reagent and 9 mL of the appropriate medium. The flask was incubated overnight at 37°C, 5% CO2. The cells were harvested using TrypLE™ reagent, and the cell concentration was adjusted to 1 x 106. The sample was divided, stained using the Tali® Viability Kit – Dead Cell Red, and analyzed both on a flow cytometer and on the Tali® Image Cytometer following the manufacturer’s recommended protocol.

Ordering Information

Sku Name Size Price Qty
T10794 Tali® Cellular Analysis Slides 50 slides USD 189.00
T10795 Tali® Cellular Analysis Slides 500 slides USD 1,694.00
T10796 Tali® Image-Based Cytometer 1 instrument USD 15,050.00
C10602 CellLight® Nucleus-GFP, BacMam 2.0 1 mL USD 372.00
A10786 Tali® Viability Kit - Dead Cell Red 1 kit USD 60.00
12605010 TrypLE™ Express Enzyme (1X), phenol red 100 mL USD 21.90

Results and Discussion

The Tali® Image Cytometer was used to measure the fluorescent protein expression level in cells that were transduced with a nuclear-targeted GFP BacMam 2.0 expression construct (CellLight® Nucleus-GFP). Four representative cell types were transduced (U2OS, 293MSR, HEKn, and CHO-S). For these cell lines, the number of cells that were expressing GFP was reported by the Tali® instrument and compared with data from the same samples analyzed on a flow cytometer. Additionally, dead cells were stained with Tali® Viability Kit – Dead Cell Red, and the dead cell population was identified on both on the Tali® cytometer and on the flow cytometer. In this part of the experiment, the number of live, GFP-expressing cells in the population was identified.

To exclude debris from the sample being analyzed, the cell size gate on the Tali® Image Cytometer was used, allowing the instrument to include only the cells of interest in the downstream fluorescence analysis. Fluorescent cells were separated from autofluorescent cells by setting a minimum fluorescence value (thresholding) on the histograms generated from the cell data by the Tali® cytometer. The fluorescence thresholds were then visually confirmed using the cell image overlays of bright-field in each fluorescence channel with circles, which indicated how each individual cell was categorized by fluorescence. By setting the threshold just to the right of the dimmest peak, cells to the left of the threshold were excluded from those counted as fluorescent in that particular channel (Figures 1A and 1B). An alternative way to identify autofluorescent cells is to measure a sample of cells that is not expressing the fluorescent protein of interest. The peak in the fluorescence histogram of nonexpressing cells represents cellular autofluorescence, and the threshold can be set just to the right of this peak for subsequent runs on an individual day. It should be noted, however, that in samples where the positive fluorescence is bright, the autofluorescence peak may be shifted to the right somewhat. In all cases, the fluorescence threshold setting was checked visually in the representative image, confirming the reported data was being derived accurately (Figures 1C and 1D).

The addition of Dead Cell Red dye (propidium iodide) provides more accurate data by removing dead cells from results, thereby measuring only viable cells expressing GFP within the population. The Tali® cytometer was able to accurately measure cells that were both viable and expressing GFP. This was accomplished using the Tali® Viability Kit – Dead Cell Red and setting the threshold on the propidium iodide (PI) channel to exclude the PI-stained dead cells. The graphical representations in Figure 2 show the percent of the total population for each cell type that were expressing GFP along with the percent of the total population that were both viable and expressing GFP. By including the Dead Cell Red dye, the population of cells that is usable for downstream processing is more obvious. It is important to note that the dead cells in the population could arise from various sources, including normal cell death in culture or cell death caused by environmental conditions (i.e., trypsinization or death induced by the transfection/transduction method chosen). These data demonstrate that the Tali® cytometer is capable of discriminating between total GFP expression in a population and GFP expression in the live population (Figure 2).

 Figure 1. Assessment of GFP-expressing cells and viability with the Tali® Image Cytometer. 293MSR cells transduced with CellLight® Nucleus-GFP BacMam constructs were analyzed on the Tali® instrument. The histograms in panels A and B show the GFP and PI fluorescence profiles for the transduced populations. As the user adjusts the thresholds for these fluorescence assignments, the visual display (panel C) is updated to reflect those cells in the population that meet the threshold requirements. Colored circles can be viewed on the image to allow easy identification of cells that were counted in a given subset of the population (Panel D). Colored circles are designated: live, GFP-expressing cells (green circles); live, non-GFP-expressing cells (blue circles); dead, GFP-expressing cells (yellow circles); objects discounted by cell size gating (black circles).

 

 Figure 2. Comparison of GFP expression and viability in cell populations between the Tali® Image Cytometer and a flow cytometer. Percent of the total population expressing nuclear-targeted GFP is shown followed by the percent of the total population that is both viable and expressing. Percentage of GFP-positive cells detected by the Tali® Image Cytometer (grey bars) or flow cytometer (green bars) are indicated.

Summary

For each cell line, the Tali® Image Cytometer produced quantitative GFP expression data, which is not possible with a visual inspection of the cells using a standard fluorescence microscope. The accuracy of these results is comparable to that obtained using a flow cytometer (Figure 2), but results are collected in a fraction of the time. In addition to producing quantitative expression data, a single Tali® cytometer experiment allows the calculation of more than one parameter—in this case, data were obtained on transduction efficiency for both the total cell population and the viable cell population. The Tali® Image Cytometer provides a bright-field image on the instrument display, allowing simultaneous visualization of the cells in brightfield and fluorescence channels. In addition, the display updates after adjusting the threshold settings for the counting and fluorescence algorithms, resulting in more confidence in the accuracy of the final data generated (Figure 3). The small yet powerful Tali® Image Cytometer offers quantitative analysis for routine end-point assays such as cell viability and two-color apoptosis/vitality assays. In addition, it is the ideal companion instrument for flow cytometry workflows, allowing confirmation of critical parameters before setting up more complicated flow cytometer runs.

 Figure 3. The Tali® Image Cytometer GFP+Viability display after measuring U2OS cells transduced with CellLight® Nuclear-GFP BacMam and stained with Tali® Viability Kit – Dead Cell Red. The assignment of each cell with a particular fluorescence channel is dependent on the threshold set in the fluorescence histogram associated with that channel. After resetting the threshold, the circles in the image on the left side of the screen will update to reflect the new fluorescence levels.