Flow Cytometry and Fluorescence-Activated Cell Sorting (FACS): Isolation of Splenic B Lymphocytes

Immunology
 

Concepts

Source: Perchet Thibaut1,2,3, Meunier Sylvain1,2,3, Sophie Novault4, Rachel Golub1,2,3
1 Unit for Lymphopoiesis, Department of Immunology, Pasteur Institute, Paris, France
2 INSERM U1223, Paris, France
3 Université Paris Diderot, Sorbonne Paris Cité, Cellule Pasteur, Paris, France
4 Flow Cytometry Platfrom, Cytometry and Biomarkers UtechS, Center for Translational Science, Pasteur Institute, Paris, France

The overall function of the immune system is to defend the body against infectious organisms and other invaders. White blood cells, or leukocytes, are the key players of the immune system. Upon infection, they are activated and initiate an immune response. Leukocytes can be divided into various sub-populations (e.g., myeloid cells, lymphocytes, dendritic cells) based on different parameters that can be biological, physical, and/or functional (e.g., size, granularity, and secretion). One way to characterize leukocytes is through their surface proteins, which are mainly receptors. Each leukocyte population expresses a specific combination of receptors (e.g., cytotoxic, activating, migration receptors) that can define subsets among populations. As the immune system encompasses a wide range of cell populations, it is essential to characterize them to decipher their participation in the immune response.

Flow cytometry (FC or FCM) is a widely used method for analyzing the expression of cell surface and intracellular molecules, characterizing and defining different cell types in a heterogenous cell mixture. Flow cytometers are composed of three main sub-systems: fluidics, optics, and electronics. The fluidics system transports the cells in a stream such that they pass in front of a laser one by one. The optics system consists of light sources (lasers) to illuminate the particles, optical filters to direct the resulting light, and fluorescent signals to appropriate detectors. Finally, the electronics system converts the detected light signals into electronic signals that can be processed by the computer. As an individual cell passes in front of the laser beam, it scatters light. A detector in front of the beam measures forward scatter (FS) and several detectors to the side measure side scatter (SC). The FS correlates with cell size and SC is proportional to the granularity of the cells. In this manner, cell populations can often be distinguished based on differences in their size and granularity alone.

In addition to analyzing a cell's size, shape, and complexity, flow cytometry is widely used for detecting the expression of cell surface receptors (1). This is accomplished by using fluorochrome-labelled monoclonal antibodies which bind to known cell-specific receptors. Upon excitation, these bound fluorochromes emit a light of specific wavelength, called emission wavelength, which can be detected and scored. Fluorescence measurements provide quantitative and qualitative data about fluorochrome-labeled cell surface receptors. Hematologists were first to use FC for the therapeutic follow up of immune cell populations (2). Now, it is used for a wide range of applications such as immunophenotyping, cell viability, gene expression, cell counting, and GFP analysis.

FACS (Fluorescent Activated Cell Sorter) is a specialized type of flow cytometry, which sorts a population of cells into subpopulation using fluorescent labelling. Just like conventional flow cytometry, first FS, SC, and fluorescent data are collected. Then, the machine applies a charge (negative or positive) and an electrostatic deflection system (electromagnets) facilitates the collection of charged droplets containing cells into appropriate tubes.

Figure 1
Figure 1: Schematic representation of FACS. Sample (1) is aspirated in the FACS (2) and passed in front of the laser (3). Cell fluorescence is sensed by fluorescence detectors (4). Finally, cells are incorporated in droplets and the cells of interest are deflected by deflection plates (5) and collected in a collection tube (6). The remaining cells go into the trash (7). Please click here to view a larger version of this figure.

The sorting aspect of the FACS presents many advantages. Many tests can help understand the role of specific cells in immune system, such as analyses of gene expression like RT-qPCR, cell cycle, or cytokine secretion. However, cells should be purified upstream to obtain clear and specific results. Here, FACS comes in useful and the desired cells can be sorted with great purity, yielding highly reliable and reproducible results. FACS can also be used to sort cells based on nuclear or other intracellular staining and according to the presence, absence, and density of surface receptors. FACS is now a standard technique for the purification of subpopulations of cells and has the ability sort up to four populations simultaneously.

This lab exercise demonstrates how to isolate splenic leukocytes and then how to specifically sort B lymphoid cells from the splenic leukocyte cell mixture using FACS.

Cite this Video | Reprints and Permissions

JoVE Science Education Database. Immunology. Flow Cytometry and Fluorescence-Activated Cell Sorting (FACS): Isolation of Splenic B Lymphocytes. JoVE, Cambridge, MA, (2019).

Procedure

1. Preparation

  1. Before beginning, put on laboratory gloves and the appropriate protective clothing.
  2. Sterilize all the dissection tools, first with a detergent and then with 70% ethanol and then dry thoroughly.
  3. Prepare 50mL of Hank's balanced salt solution (HBSS) containing 2% fetal calf serum (FCS).

2. Dissection

  1. Using a carbon dioxide delivery system, euthanize the mouse by hypoxia. Secure the euthanized mouse on a dissection plate in the supine position and perform a longitudinal laparotomy using scissors and forceps.
  2. Using forceps, move the intestines and stomach on the right side of the abdomen to expose the stomach and spleen. The spleen is attached to the stomach.
  3. Using forceps, carefully detach the spleen from the stomach and place it in the Petri dish containing 5mL of HBSS 2% FCS.

3. Immune Cell Isolation

  1. Place the spleen in a 40µm cell strainer over the same Petri dish. Crush the spleen with a plunger to dissociate it in the same dish.
  2. Transfer the dissociated spleen and the fluid into a 15mL centrifuge tube.
  3. Centrifuge the tube at 370 x g for 7 min at 10°C and discard the supernatant, avoiding the pellet.
  4. Resuspend the pellet in 2mL of potassium acetate to lyse the erythrocytes. Wait for 2 min and then make up the volume up to 15mL using HBSS 2% FCS.
  5. Centrifuge the tube again at 370 x g for 7 min at 10°C. Discard the supernatant and resuspend the pellet in 5mL of HBSS 2% FCS.
  6. Count the cells using a trypan blue staining assay and adjust the final cell concentration to 107 cells/mL using appropriate volume of HBSS 2% FCS.

4. Cell Staining

  1. Transfer 200µL of the cell suspension into six FACS tubes, labelled 1 to 6.
  2. Centrifuge the tubes at 370 x g for 7 min at 10°C and discard the supernatant avoiding the pellet.
  3. Next, prepare six novel antibody mixes by adding appropriate amount of antibody to 200µL HBSS 2% FCS according to Table 1.
  4. Then, transfer these antibody mixes to the corresponding numbered FACS tubes.
  5. Incubate the cell suspensions mixed with the antibodies for 20 minutes on ice in the dark.
  6. Add 1mL of HBSS 2% FCS to each tube and then centrifuge again at 370 x g for 3 min at 10°C.
  7. Discard the supernatant and resuspend the pellet in 200µL of HBSS 2% FCS.
  8. Transfer the resuspended pellets to new FACS tubes.

Table 1
Table 1: Antibodies mix composition. Six mixes of 200µL of HBSS + antibody were prepared for the experiment. Mix 1 is for PMT setting, mixes 2 through 5 are for compensation settings, and mix 6 is for cell sorting.

5. FACS Calibration

  1. First, turn on the sorter and perform "Fluidics Startup."
  2. Turn on the stream and then wait for 15 min for the stream to stabilize.
  3. Adjust the amplitude of the stream to obtain detached drop formation. Then click the "Sweet Spot" to complete the amplitude adjustment.
  4. Put the neutral density (N.D.) filter - 1.0 and open the "CST" interface which stands for cytometer setup and tracking.
  5. To perform daily quality control, first dilute the CST beads with FACS medium following the manufacturer's instructions and then, perform the CST control.
  6. Once CST control is complete, replace the N.D. 1.0 filter with the N.D. 2.0 filter on the cytometer.
  7. Next, dilute drop delay beads in FACS medium following the manufacturer's instructions and then load into the FACS.
  8. To ensure proper sorting perform Drop Delay-
    1. First click "Voltage" and then "Optical Filter". The right quadrant should be equal to 100%. If necessary, adjust the red laser screw on the cytometer left or right to obtain 100% in the right quadrant.
    2. Next, perform a test sort to ensure that the stream falls into the collection tube. To do so, click on "Waste Drawer" and start "Test Sort". Check that side streams fall into collection tubes. If they do not, adjust voltage until they do.
    3. Navigate to the experimental template. Then, open the "Accudrop Drop Delay" experiment and click the "Sorting Layout".
    4. Change the flow rate to obtain 1000 to 3000 events per second.
    5. Click "Voltage" and then "Optical Filter". The left quadrant should be equal to 0 and right quadrant to 100.
    6. In the "Sort Layout" window click on "Sort" and then click "Cancel". The left quadrant should be equal to 100 and right quadrant to 0. If left quadrant is less than 95 click "Auto Delay" to automatically adjust it.

6. Flow Cytometry and Purity Control

  1. Begin flow cytometry by starting with the tube 1 (unstained cells) to define the cell morphology and the negative peaks of the fluorochromes. Set up the forward and side scatter and define the voltages of each fluorescent parameter. Place the negative population in the first decade by using the grids on each dot plot.
  2. Next, load tube 2 (single color control) in the cytometer. Adjust the spectral overlap until the negative and positive population medians are aligned or use the automatic calculation software. It is important to keep the signal on scale. Compensation controls must match the experimental fluorochromes and detectors settings. Record 10,000 events.
  3. Repeat these steps with tube 3, 4, and 5 (other single color controls).
  4. Next, load tube 6 (multi-stained cells) and define cell populations of interest by using a specific gating strategy.
  5. In Sorting Layout window, select the cell population of interest. Select the cell threshold in the "Target Events" and the precision level in the "Precision". Here only one population is being sorted, however, four different populations can be sorted at the same time.
  6. Once ready click "Sort" and "OK", then wait for cell sorting.
  7. Once cell sorting is complete, perform a purity control by first pipetting 10µL of sorted cells into a new FACS tube with 90 microliters of HBSS 2% FCS.
  8. Then, load the tube the cytometer. Record and analyze the phenotypes of the cells to verify that the gating strategy worked as intended.

7. Data Analysis

  1. Open the 'FlowJo' software and drag the files for each tube in "All sample" window.
  2. Double click on a file to open it in a new window.
  3. Click on the "Polygon" and recreate gating strategy used previously.
  4. Repeat the steps with all the other files.
  5. To visualize the dot plots, click on "Layout editor" and drag the populations of interest from tube 6 and purity control in the layout editor tab. Cells should only appear in the population of interest in purity control (see Figure 2).
  6. To check the purity of B lymphocytes in the sorted cells, click on "Table editor". Drag B lymphocyte population from tube 6 and purity control in the table.
  7. On "Statistic" menu select the frequency of CD45+ cells to test the purity of this cell population, then click on "Create table".
  8. Parameter values appear in a new table. In purity control window, check the frequency of of B lymphocytes within the CD45+ cells, which should be higher than 98% (see figure 2, bottom panel).

The immune system protects the body from invading pathogens by generating leukocytes, also called white blood cells. When a pathogen successfully infects an organism, a wide variety of leukocytes are activated and this coordinated reaction is called an immune response.

Frequently, it is useful for researchers to be able to identify the specific type and number of immune cells that have been activated in response to a pathogen. Flow cytometry is a technique that allows researchers to separate cells based on specific epitopes expressed on their surfaces. This is accomplished using fluorochrome-tagged monoclonal antibodies which bind to known immune cell specific epitopes, and upon excitation, these bound fluorochromes emit a wavelength of light which can be detected and scored by a flow cytometer.

Flow cytometers are composed of three systems. The fluidic system transports cells in a stream such that they pass in front of a laser one by one. The optical system is composed of lasers and detectors which recognize the presence or absence of the fluorophores. Finally, the electronic system converts the collected optical data into electronic files for analysis.

An extension of flow cytometry is the Fluorescence-Activated Cell Sorter, or FACS, which allows for the enrichment of specific cell populations so they can be studied independently. Cell sorting is accomplished using a vibrating nozzle within the fluidics stream which forms micro droplets, each containing a single cell. Then, a detector determines whether or not fluorescent light is being emitted from each droplet, and based on that information, an electromagnet gives each cell a negative or positive charge. Next, a strong electric field sorts the differently charged droplets into separate containers. Ultimately, one of the containers will contain a homogenous population of cells based on the expression of a specific cell surface molecule.

In this video, you will learn how to use flow cytometry to isolate leukocytes from mouse spleen tissue and FACS to select for B lymphocytes.

To begin, put on laboratory gloves and the appropriate protective clothing. Next, wash a pair of dissecting scissors and forceps first with detergent and then with 70% ethanol and then dry them with a clean paper towel.

Then, add 49 milliliters of Hank's Balanced Salt Solution, or HBSS, to a 50 milliliter tube. Add one milliliter of Fetal Calf Serum, or FCS, to create an HBSS 2% FCS solution and mix by gently pipetting up and down approximately 10 times.

Next, place a euthanized mouse in the supine position on a dissection plate. With the scissors and forceps, perform a longitudinal laparotomy to access the abdominal cavity. Use the forceps to move the intestines on the right side of the abdomen to one side to expose the stomach and spleen. The spleen is attached to the stomach. Then, with a pipette, place five milliliters of the HBSS 2% FCS into a Petri dish. Using forceps, carefully detach the spleen from the stomach and place the spleen into the Petri dish.

To isolate the immune cells, first place the spleen on a 40 micron cell strainer in a Petri dish. Crush the spleen with a plunger to dissociate it into the dish. Then, pipette the dissociated spleen and fluid from the Petri dish into a 15 milliliter centrifuge tube. Centrifuge the tube at 370 times g for seven minutes at 10 degrees Celsius and then retrieve the tube carefully so as not to disturb the pellet.

Now, remove the supernatant, avoiding the pellet, and discard the liquid in an appropriate waste container. Then, add two milliliters of ACK lysing buffer into the centrifuge tube to resuspend and lyse the erythrocytes. Wait two minutes and then add HBSS 2% FCS to obtain a total volume of 15 milliliters. Repeat the centrifugation. Retrieve the tube carefully and discard the supernatant. Resuspend the pellet again in five milliliters of HBSS 2% FCS.

To count the resuspended cells, dilute five microliters of the cell suspension with five microliters of Trypan Blue. Then, gently deposit a five microliter drop of this diluted cell suspension between the coverglass and the Malassez slide. Now, under a microscope at 40X magnification, count the number of cells present. Then, adjust the cell concentration to 10 to the seventh cells per milliliter by adding the appropriate volume of HBSS 2% FCS.

To stain the immune cells, start by labeling six FACS tubes from one to six. Then, transfer 200 microliters of the cell solution into each of the six tubes. Centrifuge these tubes at 370 times g for seven minutes at 10 degrees Celsius and remove the supernatant.

Then, label six new FACS tubes as one through six and pipette 200 microliters of HBSS 2% FCS into each. Prepare the six novel antibody mixes by adding the appropriate amount of antibody to each tube according to table one. Mix one is for unstained cells with no addition of antibody. Mixes two through five each contain a different single antibody for compensation settings. Mix six contains all four antibodies for multi-stained cells to be used for sorting.

Next, transfer these antibody mixes to the corresponding numbered FACS tubes. Incubate these solutions for 20 minutes at four degrees Celsius or on ice in the dark. Next, add one milliliter of HBSS 2% FCS to each tube and then centrifuge again. Discard the supernatant and then resuspend the pellets in 200 microliters of HBSS 2% FCS. Finally, transfer the resuspended pellets to new labeled FACS tubes.

To perform FACS, first turn on the sorter. Then, select the cytometer menu and click fluidics startup. Follow the instructions on the screen.

On the stream tab, click on the red cross to turn on the stream and then wait 15 minutes for the stream to stabilize. Adjust the amplitude of the stream until you see a clear detached drop appear on the stream tab. Then, click sweet spot to complete the amplitude adjustment. Insert the Neutral Density, or ND, filter 1.0 in front of the laser.

Open the cytometer menu at the top of the screen and select CST, which stands for Cytometer Setup and Tracking. To perform daily quality control, first dilute CST beads with FACS medium in a FACS tube following the manufacturer's instructions. Then, load the tube into the machine and perform the CST control by clicking run on the CST tab.

When the CST control is complete, replace the ND 1.0 filter with the ND 2.0 filter on the cytometer. Next, dilute drop delay beads in FACS medium following the manufacturer's instructions and then load the tube into the FACS. To ensure proper sorting, perform drop delay by first clicking voltage and then optical filter. The right quadrant of the optical filter should be equal to 100%, indicating that 100% of the drops are registered by the machine. If necessary, adjust the red laser screw on the cytometer left or right to obtain 100% in the right quadrant. It is important to ensure that the stream falls into the collection tube. To do so, perform a test sort by clicking on waste drawer and then test sort. Check that the side streams fall into the collection tubes. If they do not, adjust the voltage under the sorting tab until they do.

Navigate to the experimental template by selecting the browser tab and clicking shared view. Then, open the Accudrop_DROP DELAY experiment and click the sorting layout button. Now, change the threshold rate on the acquisition dashboard by manipulating the flow rate until it reaches 3,000 events per second. Click voltage and then click optical filter. The left quadrant should be equal to zero and right quadrant equal to 100.

Finally, in the sort layout window, click sort and then click cancel. The left quadrant should be equal to 100 and the right quadrant equal to zero. If the left quadrant is less than 95, click auto delay to instruct the software to automatically increase the voltage to obtain 100% of the drops in the left quadrant.

To begin flow cytometry, we will first use unstained cells to define the cell morphology and the negative peaks of the fluorochromes. To do so, place tube one containing unstained cells in the machine and under the acquisition dashboard tab click load. In the cytometer tab, adjust the forward and side scatter voltages until you see your cell population as a dense concentration of dots on the screen. Lymphocytes are small cells, so they will have a low forward scatter and low side scatter.

Next, remove background fluorescence by adjusting the voltage for the fluorochromes in the cytometer tab until the cell populations at a negative level are in the first decade in the global worksheet tab. In the cytometer menu, click on view configuration and verify that all of the fluorochromes are present. Next, place tube two in the cytometer and click load. Adjust the spectral overlap in the cytometer tab until the negative and positive population medians are aligned in the global worksheet tab. On the acquisition tab, set the events to record parameter to 10,000 and click record. Repeat these steps with tubes three, four, and five.

Next, load tube six which contains the multi-stained cells. To isolate B lymphocytes, first set up the parameters to sort the cells based on their morphology. In the first window, plot FSC-A forward scatter area on the y-axis and SSC-A side scatter area on the x-axis. In the scatter plot, each dot represents a cell. Click on polygon gate on the global worksheet and then select the population with a low forward scatter and an intermediate side scatter. On a new dot plot window, right-click on the window and select show populations from the menu and click P1.

Then, in the new window, gate the viable CD45 positive cells by plotting viability on the y-axis and CD45 on the x-axis. Use polygon gate to circle the cells with a low viability and high CD45 signal and select P2 to display the selected cells in a new window. In the next window, gate for CD45 positive leukocytes, excluding T lymphocytes. With CD45 on the x-axis and CD3 on the y-axis, circle the population with a high CD45 signal and low negative CD3 signal and select P3. Finally, gate for CD19 positive cells which identify the B lymphocytes. With CD19 on the y-axis and CD3 on the x-axis, circle the population with a high CD19 signal and a low negative CD3 signal and select P4.

All the sorting parameters are now set. Next, in the sorting layout window, select your cell population of interest- P4, which is the fourth population that was gated, and tells the machine to only sort B lymphocytes. Set target events to 10,000 cells and set precision to purity. We are only sorting one population. However, up to four different populations can be sorted at the same time. Once ready, click sort and OK. Then, wait for cell sorting.

Once cell sorting is complete, perform a purity control by pipetting 10 microliters of the sorted cells into a new FACS tube with 90 microliters of HBSS 2% FCS. Place the tube in the cytometer, click load and then click record to analyze the phenotypes of the cells to verify that the gating strategy worked as intended.

Now, we will analyze the sorted cells to determine the percentage of B lymphocytes among the leukocytes that were isolated from the mouse spleen. To start, double click on the FlowJo icon and drag the files for each tube into the all sample window.

Click on polygon and recreate the gating strategies that were used in the previous section. Next, click layout editor and drag the B lymphocyte populations of interest from tube six and the purity control into the layout editor tab. Dot plots representing B lymphocytes will appear. In this example, the plot on the top right represents the sorted B lymphocytes from the total spleen cell suspension and the plot on the bottom right is the purity control. Cells should only appear in the population of interest in the purity control.

To check the purity of B lymphocytes in the sorted cells, click on table editor. Drag the B lymphocyte population from tube six and purity control in the table. On the statistic menu, select frequency of CD45 positive cells to test the purity of this cell population. Then, click on create table. Parameter values appear in a new table. In the purity control window, check the frequency of B lymphocytes within the CD45 positive cells, which should be higher than 98%.

Results

In this protocol, we purified splenic B lymphocytes using FACS technology. We first isolated leukocytes from the spleen and stained them. Using a combination of B cell surface markers, we created a gating strategy to sort them (Figure 2, top panel). At the end of the experiment we verified if cells in the collection tube were B cells via a "purity test". We kept the same gating strategy and observed that more than 98% of the cells were indeed B cells (Figure 2, bottom panel). Thus, FACS is an effective protocol to isolate immune cell populations with a high degree of purity. Collected cells can then be used for downstream experiments such as cell culture, RT-qPCR, and cytotoxicity assays.

Figure 2
Figure 2: Gating strategy and testing post-sort purity. (A) Cells were first gated based on their morphology (left: FSC-A, SSC-A), then only alive (middle left: viability, CD45), CD45+ cells (CD45, CD3) were plotted against CD19 and CD3. Only CD19+ cells were sorted. (B) Purity test results of a fraction of cells obtained after cell sorting. Please click here to view a larger version of this figure.

Applications and Summary

Flow cytometry is a first-hand technique to characterize and sort immune cell populations with a high degree of purity. It is primordial tool in research field as it allows enrichment of specific cell populations and to decipher the immune response to pathogens. With the increase in number of available fluorochromes and cytometers, the number of detectable parameters is highly increased. As a result, bioinformatic analysis of FACS data has begun to emerge and have opened new horizons to flow cytometry (3). Flow cytometry offers other applications in haematology and oncology (4) where it is used for developing diagnostic tools.

References

  1. Lanier, L. L. Just the FACS. The Journal of Immunology, 193 (5), 2043-2044 (2014).
  2. Walker, J. M. Epiblast Stem Cells IN Series Editor.
  3. Tung, J. W., Heydari, K., Tirouvanziam, R., Sahaf, B., Parks. D. R., Herzenberg, L. A., and Herzenberg. L. A. Modern Flow Cytometry: A Practical Approach. Clinics in Laboratory Medicine. 27 (3), 453-468 (2007).
  4. Walker, J. M. Tumor Angiogenesis Assays IN Series Editor.

1. Preparation

  1. Before beginning, put on laboratory gloves and the appropriate protective clothing.
  2. Sterilize all the dissection tools, first with a detergent and then with 70% ethanol and then dry thoroughly.
  3. Prepare 50mL of Hank's balanced salt solution (HBSS) containing 2% fetal calf serum (FCS).

2. Dissection

  1. Using a carbon dioxide delivery system, euthanize the mouse by hypoxia. Secure the euthanized mouse on a dissection plate in the supine position and perform a longitudinal laparotomy using scissors and forceps.
  2. Using forceps, move the intestines and stomach on the right side of the abdomen to expose the stomach and spleen. The spleen is attached to the stomach.
  3. Using forceps, carefully detach the spleen from the stomach and place it in the Petri dish containing 5mL of HBSS 2% FCS.

3. Immune Cell Isolation

  1. Place the spleen in a 40µm cell strainer over the same Petri dish. Crush the spleen with a plunger to dissociate it in the same dish.
  2. Transfer the dissociated spleen and the fluid into a 15mL centrifuge tube.
  3. Centrifuge the tube at 370 x g for 7 min at 10°C and discard the supernatant, avoiding the pellet.
  4. Resuspend the pellet in 2mL of potassium acetate to lyse the erythrocytes. Wait for 2 min and then make up the volume up to 15mL using HBSS 2% FCS.
  5. Centrifuge the tube again at 370 x g for 7 min at 10°C. Discard the supernatant and resuspend the pellet in 5mL of HBSS 2% FCS.
  6. Count the cells using a trypan blue staining assay and adjust the final cell concentration to 107 cells/mL using appropriate volume of HBSS 2% FCS.

4. Cell Staining

  1. Transfer 200µL of the cell suspension into six FACS tubes, labelled 1 to 6.
  2. Centrifuge the tubes at 370 x g for 7 min at 10°C and discard the supernatant avoiding the pellet.
  3. Next, prepare six novel antibody mixes by adding appropriate amount of antibody to 200µL HBSS 2% FCS according to Table 1.
  4. Then, transfer these antibody mixes to the corresponding numbered FACS tubes.
  5. Incubate the cell suspensions mixed with the antibodies for 20 minutes on ice in the dark.
  6. Add 1mL of HBSS 2% FCS to each tube and then centrifuge again at 370 x g for 3 min at 10°C.
  7. Discard the supernatant and resuspend the pellet in 200µL of HBSS 2% FCS.
  8. Transfer the resuspended pellets to new FACS tubes.

Table 1
Table 1: Antibodies mix composition. Six mixes of 200µL of HBSS + antibody were prepared for the experiment. Mix 1 is for PMT setting, mixes 2 through 5 are for compensation settings, and mix 6 is for cell sorting.

5. FACS Calibration

  1. First, turn on the sorter and perform "Fluidics Startup."
  2. Turn on the stream and then wait for 15 min for the stream to stabilize.
  3. Adjust the amplitude of the stream to obtain detached drop formation. Then click the "Sweet Spot" to complete the amplitude adjustment.
  4. Put the neutral density (N.D.) filter - 1.0 and open the "CST" interface which stands for cytometer setup and tracking.
  5. To perform daily quality control, first dilute the CST beads with FACS medium following the manufacturer's instructions and then, perform the CST control.
  6. Once CST control is complete, replace the N.D. 1.0 filter with the N.D. 2.0 filter on the cytometer.
  7. Next, dilute drop delay beads in FACS medium following the manufacturer's instructions and then load into the FACS.
  8. To ensure proper sorting perform Drop Delay-
    1. First click "Voltage" and then "Optical Filter". The right quadrant should be equal to 100%. If necessary, adjust the red laser screw on the cytometer left or right to obtain 100% in the right quadrant.
    2. Next, perform a test sort to ensure that the stream falls into the collection tube. To do so, click on "Waste Drawer" and start "Test Sort". Check that side streams fall into collection tubes. If they do not, adjust voltage until they do.
    3. Navigate to the experimental template. Then, open the "Accudrop Drop Delay" experiment and click the "Sorting Layout".
    4. Change the flow rate to obtain 1000 to 3000 events per second.
    5. Click "Voltage" and then "Optical Filter". The left quadrant should be equal to 0 and right quadrant to 100.
    6. In the "Sort Layout" window click on "Sort" and then click "Cancel". The left quadrant should be equal to 100 and right quadrant to 0. If left quadrant is less than 95 click "Auto Delay" to automatically adjust it.

6. Flow Cytometry and Purity Control

  1. Begin flow cytometry by starting with the tube 1 (unstained cells) to define the cell morphology and the negative peaks of the fluorochromes. Set up the forward and side scatter and define the voltages of each fluorescent parameter. Place the negative population in the first decade by using the grids on each dot plot.
  2. Next, load tube 2 (single color control) in the cytometer. Adjust the spectral overlap until the negative and positive population medians are aligned or use the automatic calculation software. It is important to keep the signal on scale. Compensation controls must match the experimental fluorochromes and detectors settings. Record 10,000 events.
  3. Repeat these steps with tube 3, 4, and 5 (other single color controls).
  4. Next, load tube 6 (multi-stained cells) and define cell populations of interest by using a specific gating strategy.
  5. In Sorting Layout window, select the cell population of interest. Select the cell threshold in the "Target Events" and the precision level in the "Precision". Here only one population is being sorted, however, four different populations can be sorted at the same time.
  6. Once ready click "Sort" and "OK", then wait for cell sorting.
  7. Once cell sorting is complete, perform a purity control by first pipetting 10µL of sorted cells into a new FACS tube with 90 microliters of HBSS 2% FCS.
  8. Then, load the tube the cytometer. Record and analyze the phenotypes of the cells to verify that the gating strategy worked as intended.

7. Data Analysis

  1. Open the 'FlowJo' software and drag the files for each tube in "All sample" window.
  2. Double click on a file to open it in a new window.
  3. Click on the "Polygon" and recreate gating strategy used previously.
  4. Repeat the steps with all the other files.
  5. To visualize the dot plots, click on "Layout editor" and drag the populations of interest from tube 6 and purity control in the layout editor tab. Cells should only appear in the population of interest in purity control (see Figure 2).
  6. To check the purity of B lymphocytes in the sorted cells, click on "Table editor". Drag B lymphocyte population from tube 6 and purity control in the table.
  7. On "Statistic" menu select the frequency of CD45+ cells to test the purity of this cell population, then click on "Create table".
  8. Parameter values appear in a new table. In purity control window, check the frequency of of B lymphocytes within the CD45+ cells, which should be higher than 98% (see figure 2, bottom panel).

The immune system protects the body from invading pathogens by generating leukocytes, also called white blood cells. When a pathogen successfully infects an organism, a wide variety of leukocytes are activated and this coordinated reaction is called an immune response.

Frequently, it is useful for researchers to be able to identify the specific type and number of immune cells that have been activated in response to a pathogen. Flow cytometry is a technique that allows researchers to separate cells based on specific epitopes expressed on their surfaces. This is accomplished using fluorochrome-tagged monoclonal antibodies which bind to known immune cell specific epitopes, and upon excitation, these bound fluorochromes emit a wavelength of light which can be detected and scored by a flow cytometer.

Flow cytometers are composed of three systems. The fluidic system transports cells in a stream such that they pass in front of a laser one by one. The optical system is composed of lasers and detectors which recognize the presence or absence of the fluorophores. Finally, the electronic system converts the collected optical data into electronic files for analysis.

An extension of flow cytometry is the Fluorescence-Activated Cell Sorter, or FACS, which allows for the enrichment of specific cell populations so they can be studied independently. Cell sorting is accomplished using a vibrating nozzle within the fluidics stream which forms micro droplets, each containing a single cell. Then, a detector determines whether or not fluorescent light is being emitted from each droplet, and based on that information, an electromagnet gives each cell a negative or positive charge. Next, a strong electric field sorts the differently charged droplets into separate containers. Ultimately, one of the containers will contain a homogenous population of cells based on the expression of a specific cell surface molecule.

In this video, you will learn how to use flow cytometry to isolate leukocytes from mouse spleen tissue and FACS to select for B lymphocytes.

To begin, put on laboratory gloves and the appropriate protective clothing. Next, wash a pair of dissecting scissors and forceps first with detergent and then with 70% ethanol and then dry them with a clean paper towel.

Then, add 49 milliliters of Hank's Balanced Salt Solution, or HBSS, to a 50 milliliter tube. Add one milliliter of Fetal Calf Serum, or FCS, to create an HBSS 2% FCS solution and mix by gently pipetting up and down approximately 10 times.

Next, place a euthanized mouse in the supine position on a dissection plate. With the scissors and forceps, perform a longitudinal laparotomy to access the abdominal cavity. Use the forceps to move the intestines on the right side of the abdomen to one side to expose the stomach and spleen. The spleen is attached to the stomach. Then, with a pipette, place five milliliters of the HBSS 2% FCS into a Petri dish. Using forceps, carefully detach the spleen from the stomach and place the spleen into the Petri dish.

To isolate the immune cells, first place the spleen on a 40 micron cell strainer in a Petri dish. Crush the spleen with a plunger to dissociate it into the dish. Then, pipette the dissociated spleen and fluid from the Petri dish into a 15 milliliter centrifuge tube. Centrifuge the tube at 370 times g for seven minutes at 10 degrees Celsius and then retrieve the tube carefully so as not to disturb the pellet.

Now, remove the supernatant, avoiding the pellet, and discard the liquid in an appropriate waste container. Then, add two milliliters of ACK lysing buffer into the centrifuge tube to resuspend and lyse the erythrocytes. Wait two minutes and then add HBSS 2% FCS to obtain a total volume of 15 milliliters. Repeat the centrifugation. Retrieve the tube carefully and discard the supernatant. Resuspend the pellet again in five milliliters of HBSS 2% FCS.

To count the resuspended cells, dilute five microliters of the cell suspension with five microliters of Trypan Blue. Then, gently deposit a five microliter drop of this diluted cell suspension between the coverglass and the Malassez slide. Now, under a microscope at 40X magnification, count the number of cells present. Then, adjust the cell concentration to 10 to the seventh cells per milliliter by adding the appropriate volume of HBSS 2% FCS.

To stain the immune cells, start by labeling six FACS tubes from one to six. Then, transfer 200 microliters of the cell solution into each of the six tubes. Centrifuge these tubes at 370 times g for seven minutes at 10 degrees Celsius and remove the supernatant.

Then, label six new FACS tubes as one through six and pipette 200 microliters of HBSS 2% FCS into each. Prepare the six novel antibody mixes by adding the appropriate amount of antibody to each tube according to table one. Mix one is for unstained cells with no addition of antibody. Mixes two through five each contain a different single antibody for compensation settings. Mix six contains all four antibodies for multi-stained cells to be used for sorting.

Next, transfer these antibody mixes to the corresponding numbered FACS tubes. Incubate these solutions for 20 minutes at four degrees Celsius or on ice in the dark. Next, add one milliliter of HBSS 2% FCS to each tube and then centrifuge again. Discard the supernatant and then resuspend the pellets in 200 microliters of HBSS 2% FCS. Finally, transfer the resuspended pellets to new labeled FACS tubes.

To perform FACS, first turn on the sorter. Then, select the cytometer menu and click fluidics startup. Follow the instructions on the screen.

On the stream tab, click on the red cross to turn on the stream and then wait 15 minutes for the stream to stabilize. Adjust the amplitude of the stream until you see a clear detached drop appear on the stream tab. Then, click sweet spot to complete the amplitude adjustment. Insert the Neutral Density, or ND, filter 1.0 in front of the laser.

Open the cytometer menu at the top of the screen and select CST, which stands for Cytometer Setup and Tracking. To perform daily quality control, first dilute CST beads with FACS medium in a FACS tube following the manufacturer's instructions. Then, load the tube into the machine and perform the CST control by clicking run on the CST tab.

When the CST control is complete, replace the ND 1.0 filter with the ND 2.0 filter on the cytometer. Next, dilute drop delay beads in FACS medium following the manufacturer's instructions and then load the tube into the FACS. To ensure proper sorting, perform drop delay by first clicking voltage and then optical filter. The right quadrant of the optical filter should be equal to 100%, indicating that 100% of the drops are registered by the machine. If necessary, adjust the red laser screw on the cytometer left or right to obtain 100% in the right quadrant. It is important to ensure that the stream falls into the collection tube. To do so, perform a test sort by clicking on waste drawer and then test sort. Check that the side streams fall into the collection tubes. If they do not, adjust the voltage under the sorting tab until they do.

Navigate to the experimental template by selecting the browser tab and clicking shared view. Then, open the Accudrop_DROP DELAY experiment and click the sorting layout button. Now, change the threshold rate on the acquisition dashboard by manipulating the flow rate until it reaches 3,000 events per second. Click voltage and then click optical filter. The left quadrant should be equal to zero and right quadrant equal to 100.

Finally, in the sort layout window, click sort and then click cancel. The left quadrant should be equal to 100 and the right quadrant equal to zero. If the left quadrant is less than 95, click auto delay to instruct the software to automatically increase the voltage to obtain 100% of the drops in the left quadrant.

To begin flow cytometry, we will first use unstained cells to define the cell morphology and the negative peaks of the fluorochromes. To do so, place tube one containing unstained cells in the machine and under the acquisition dashboard tab click load. In the cytometer tab, adjust the forward and side scatter voltages until you see your cell population as a dense concentration of dots on the screen. Lymphocytes are small cells, so they will have a low forward scatter and low side scatter.

Next, remove background fluorescence by adjusting the voltage for the fluorochromes in the cytometer tab until the cell populations at a negative level are in the first decade in the global worksheet tab. In the cytometer menu, click on view configuration and verify that all of the fluorochromes are present. Next, place tube two in the cytometer and click load. Adjust the spectral overlap in the cytometer tab until the negative and positive population medians are aligned in the global worksheet tab. On the acquisition tab, set the events to record parameter to 10,000 and click record. Repeat these steps with tubes three, four, and five.

Next, load tube six which contains the multi-stained cells. To isolate B lymphocytes, first set up the parameters to sort the cells based on their morphology. In the first window, plot FSC-A forward scatter area on the y-axis and SSC-A side scatter area on the x-axis. In the scatter plot, each dot represents a cell. Click on polygon gate on the global worksheet and then select the population with a low forward scatter and an intermediate side scatter. On a new dot plot window, right-click on the window and select show populations from the menu and click P1.

Then, in the new window, gate the viable CD45 positive cells by plotting viability on the y-axis and CD45 on the x-axis. Use polygon gate to circle the cells with a low viability and high CD45 signal and select P2 to display the selected cells in a new window. In the next window, gate for CD45 positive leukocytes, excluding T lymphocytes. With CD45 on the x-axis and CD3 on the y-axis, circle the population with a high CD45 signal and low negative CD3 signal and select P3. Finally, gate for CD19 positive cells which identify the B lymphocytes. With CD19 on the y-axis and CD3 on the x-axis, circle the population with a high CD19 signal and a low negative CD3 signal and select P4.

All the sorting parameters are now set. Next, in the sorting layout window, select your cell population of interest- P4, which is the fourth population that was gated, and tells the machine to only sort B lymphocytes. Set target events to 10,000 cells and set precision to purity. We are only sorting one population. However, up to four different populations can be sorted at the same time. Once ready, click sort and OK. Then, wait for cell sorting.

Once cell sorting is complete, perform a purity control by pipetting 10 microliters of the sorted cells into a new FACS tube with 90 microliters of HBSS 2% FCS. Place the tube in the cytometer, click load and then click record to analyze the phenotypes of the cells to verify that the gating strategy worked as intended.

Now, we will analyze the sorted cells to determine the percentage of B lymphocytes among the leukocytes that were isolated from the mouse spleen. To start, double click on the FlowJo icon and drag the files for each tube into the all sample window.

Click on polygon and recreate the gating strategies that were used in the previous section. Next, click layout editor and drag the B lymphocyte populations of interest from tube six and the purity control into the layout editor tab. Dot plots representing B lymphocytes will appear. In this example, the plot on the top right represents the sorted B lymphocytes from the total spleen cell suspension and the plot on the bottom right is the purity control. Cells should only appear in the population of interest in the purity control.

To check the purity of B lymphocytes in the sorted cells, click on table editor. Drag the B lymphocyte population from tube six and purity control in the table. On the statistic menu, select frequency of CD45 positive cells to test the purity of this cell population. Then, click on create table. Parameter values appear in a new table. In the purity control window, check the frequency of B lymphocytes within the CD45 positive cells, which should be higher than 98%.

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