Adoptive Cell Transfer: Introducing Donor Mouse Splenocytes to a Host Mouse and Assessing Success via FACS

Immunology

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Concepts

Source: Meunier Sylvain1,2,3, Perchet Thibaut1,2,3, 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

Adoptive cell transfer is a method for introducing cells into a patient or study organism in order to treat a disease or study a biological process, such as haematopoiesis. Aims of adoptive transfer are various; it can be used in fundamental biology as well as in medical sciences (1, 2). In mouse models, migration and distribution of transferred cells can be studied and followed by a tracking system (cell surface marker, staining by CFSE, etc.). In cancer studies on mouse models, transfer of specific cell populations can be used as experimental treatment against tumors. Another example for this technique is creation of chimeric mice by transfer of bone marrow cells to irradiated mice or mice with a severe immunodeficiency phenotype. This mouse model can be used to assess the impact of gene deletion on a specific cell population for instance. Transfer of bone borrow cells is also used in human medical treatment. When patients are irradiated in case of cancer therapy, adoptive transfer of bone marrow allows immune system reconstitution.

The first step in this technique is to obtain the cell population of interest. The technique chosen to isolate this population depends on the level of specificity of the targeted population. The largest level of selection is the whole organ, in which all cell populations present in the organ are taken. A more precise method is selection of a target cell population, often selected by one cell surface marker. The ideal method to sort cells in this case is by magnetic sorting. Finally, the most stringent level is the selection of cells by several cell surface markers to sort very specific cell populations. Flow cytometry sorting is the most popular method for this level of selection. Once population of interest is obtained, it can be transferred to the host. Before adoptive transfer it is essential to ensure compatibility between host and donor. Indeed, regardless of transfer goal, compatibility is crucial to assure cells adoption by the host without cells rejection.

In this lab exercise, we demonstrate the adoptive cell transfer technique by transferring splenocytes from a CD45.2 mouse into a CD45.1 Ragγc mouse (lacking lymphocytes) and four days later confirm the splenocytes transfer using flow cytometry (see Figure 1).

Figure 1
Figure 1: Schematic representation of adoptive transfer. (1) Splenocytes are isolated from CD45.2 mice and (2) transferred in CD45.1 Ragγc mouse, control mouse is injected with PBS only. (3) 4 days after adoptive transfer, splenocytes are recovered from mice and (4) analyzed by flow cytometry. Please click here to view a larger version of this figure.

Cite this Video

JoVE Science Education Database. Immunology. Adoptive Cell Transfer: Introducing Donor Mouse Splenocytes to a Host Mouse and Assessing Success via FACS. JoVE, Cambridge, MA, (2020).

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 50 mL 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 on the Petri dish containing 5 mL of HBSS 2% FCS.

3. Immune Cell Isolation

  1. Place the spleen on a 40 µm cell strainer over the Petri dish. Crush the spleen with a plunger to dissociate it.
  2. Recover the adhered cells by rinsing the plunger and the strainer with 1 mL of HBSS 2% FCS.
  3. Transfer the dissociated spleen and the fluid into a 15 mL centrifuge tube.
  4. Wash the Petri dish with 5 milliliters of HBSS 2% FCS and transfer the fluid to the 15 mL tube.
  5. Centrifuge the tube at 370 x g for 7 min at 10°C and discard the supernatant avoiding the pellet.
  6. Resuspend the pellet in 2 mL of potassium ammonium chloride pipet up and down to resuspend the pellet and lyse the erythrocytes.
  7. Wait for 2 min and add HBSS 2% FCS to the resuspended pellet to obtain the volume up to 14 mL.
  8. Centrifuge the tube again at 370 x g for 7 min at 10°C. Discard the supernatant and resuspend the pellet in 5 mL of HBSS 2% FCS by pipetting up and down.
  9. Count the cells using trypan blue staining assay and adjust the final cell concentration to 107 cells/mL using appropriate volume of HBSS 2% FCS.

4. Adoptive Transfer

  1. Transfer 2 mL of cell suspension obtained in a 5 mL collection tube.
  2. Centrifuge the tube at 370 x g for 7 min at 10°C and then discard the supernatant.
  3. Resuspend the pellet in 2 mL of PBS and centrifuge the tube at 370 x g for 7 min at 10°C.
  4. Discard supernatant and resuspend pellet in 200 µL of PBS.
  5. Using a 0.5 mL syringe with a 29G needle inject 200 µL of cell suspension into the experimental mouse intravenously into the retro-orbital blood sinus.
  6. As a control, inject a second mouse in the same blood sinus with 200 µL of phosphate buffered saline.

5. Cells Harvest and Staining

  1. Four days after the adoptive transfer, euthanize mice and remove the spleen.
  2. Harvest the splenocytes as described in section 3.
  3. Transfer 100 µL of cell suspensions from each mouse into two FACS tubes, labeled "control" and "transferred".
  4. Centrifuge the tube at 370 x g for 7 min at 10°C and then discard the supernatants.
  5. Prepare a mix containing the four antibodies at the dilutions listed in Table 1.
Antibodies Fluorochrome Dilution
CD45.1 BV711 1/200
CD45.2 APCCy7 1/400
CD4 BV786 1/1600
CD3 BV421 1/200

Table 1: Antibodies mix composition. Four antibodies cocktails preparation using concentrated antibody-fluorescent conjugates and HBSS.

  1. Add 100 µL of the mix to each tube, and then incubate for 20 min on ice in the dark.
  2. Add 1 mL of HBSS 2%FCS and then centrifuge the tubes at 370 x g for 3 min at 10°C.
  3. Discard the supernatants and resuspend the pellets in 200 µL of HBSS 2% FCS.
  4. Transfer the resuspended cells to new, labelled FACS tubes.
  5. Using flow cytometry, as shown in FACS protocol, evaluate the presence of CD45.2 positive lymphocytes.

6. Data Analysis

  1. Open the "FlowJo" software and drag the files for each tube in "All sample" window.
  2. Double click on the "transferred" file to display the cells recorded from that sample on a dot plot that displays forward scatter "SSC-A" on the Y axis and side scatter "FSC-A" on the X axis.
  3. Click on "polygon" and create a gating strategy to select lymphocytes, then distinguish donor and host cells using cell surface markers (CD45.1, CD45.2), and then characterize CD45.2+ cell population (CD3, CD4).
  4. Repeat the analysis steps with "control mouse" file.
  5. To visualize a cell population, click on "Layout editor".
  6. Drag the "transferred cells" and the "transferred CD4 cells" population from "transferred" and "control" files into the "Layout Editor tab".
  7. A dot plot representing CD45.2+ cells and CD4 lymphocytes will appear.
  8. CD45.2 transferred cells should only appear in the "transferred mouse" dot plot.

Adoptive cell transfer is a method for introducing cells of interest into an organism. It is a powerful technique to study various biological mechanisms, including the action of specific classes of immune cells. In addition, adoptive transfer is a promising novel treatment for numerous conditions, such as those requiring bone marrow transplants or cancer treatments where a patient's own T-cells can be extracted, altered to recognize and destroy the cancerous cells, and then returned to the body to fight tumors.

In the laboratory, animal models are often used to study adoptive transfer. For example, CD45.1 Rag gamma-c knockout mice lack fundamental receptors for many cytokines, which are essential for normal differentiation of hematopoietic stem cells into lymphocytes. As a result, the knockout mice have a compromised lymphocyte development and do not have natural killer, or NK, cells, T-cells, or B-cells.

Adoptive transfer can be used to introduce the missing immune cells into these compromised mice, by first harvesting donor mouse tissue containing high concentrations of immune cells, such as the spleen. The tissue is then dissociated and a variety of spleen cells, including the immune cells, are isolated. Next, unwanted erythrocytes, or red blood cells, can be lysed via the addition of ammonium chloride potassium lysing buffer and the remaining white blood cells, or splenocytes, are then separated from the cell debris using centrifugation.

Finally, the purified splenocytes are injected into the immunocompromised mice, facilitating detailed studies of these cells' functions. Several days later, the success of the adoptive immune cell transfer can be confirmed by first isolating and preparing the host splenoncytes in the same manner as the donor tissue. Then, these cells are stained using labeled antibodies against the donor immune cell markers so that they can be verified and sorted using FACS.

To begin, put on laboratory gloves and the appropriate protective equipment. Next, wash a pair of forceps and dissecting scissors first with a detergent and then with 70% ethanol and then dry them with a clean paper towel. Prepare 50 milliliters of Hank's Balanced Salt Solution, or HBSS, with 2% Fetal Calf Serum, or FCS, by combining one milliliter of FCS with 49 milliliters of HBSS in a 50 milliliter tube. Mix by gently pipetting the solution up and down approximately 10 times.

Dissect the euthanized mouse and remove its spleen as demonstrated in the JoVE video protocol FACS technology for splenic B lymphocytes separation. To isolate immune cells, first place the spleen on a 40 micrometer cell strainer in a petri dish. Crush the spleen with a plunger to dissociate it into the dish. Recover the adhered cells by rinsing the plunger and the strainer with 1 milliliter of HBSS 2% FCS. Then, pipette the dissociated spleen and fluid from the petri dish into a 50 milliliter centrifuge tube. Wash the petri dish with 5 milliliters of HBSS 2% FCS and transfer the fluid to the 15 milliliter 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 without disturbing the pellet and discard the liquid in an appropriate waste container. Then, add two milliliters of ammonium chloride potassium lysing buffer to the centrifuge tube and pipette up and down to resuspend the pellet and lyse the erythrocytes. Wait for two minutes and then add HBSS 2% FCS to the resuspended pellet to obtain a total value of 14 milliliters. Repeat the centrifugation. Retrieve the tube carefully and discard the supernatant. Then, resuspend the pellet in 5 milliliters HBSS 2% FCS by pipetting up and down. Next, count the cells in suspension. Add five microliters of trypan blue to five microliters of cell suspension and mix well by pipetting. Then, gently deposit a five microliter drop of diluted cell suspension between the cover glass and the Malassez slide. With the microscope set to 40X magnification, count the number of cells. Adjust the cell concentration to 10 to the seven cells per milliliter by adding the appropriate volume of HBSS 2% FCS.

To begin the adoptive transfer, transfer two milliliters of the cell suspension to a five milliliter collection tube. Centrifuge the tube at 370 times g for seven minutes at 10 degrees Celsius and then discard the supernatant. Next, resuspend the pellet in two milliliters of phosphate buffered saline and centrifuge the tube at 370 times g for seven minutes at 10 degrees Celsius. Discard the supernatant. Then, resuspend the pellet in 200 microliters of phosphate buffered saline. Using a 0.5 milliliter syringe with a 29-gauge needle, inject 200 microliters of cell suspension into the experimental mouse intravenously into the retro-orbital blood sinus.

Four days after the adoptive transfer, euthanize the mice and remove the spleens. Then, harvest the immune cells as described in section three. Next, transfer 100 microliters of cell suspension from each mouse into two FACS tubes labeled control and transferred. Centrifuge the tubes at 370 times g for seven minutes at 10 degrees Celsius and then discard the supernatants. Now, prepare a mix containing the four antibodies at the dilution listed in table one. Add 100 microliters of the mix to each tube and then incubate for 20 minutes on ice in the dark. Next, add one milliliter of HBSS 2% FCS to each tube and then centrifuge the tubes at 370 times g for three minutes at 10 degrees Celsius. Discard the supernatants and then resuspend the pellets in 200 microliters of HBSS 2% FCS. Transfer the resuspended cells to new labeled FACS tubes. Now, use flow cytometry as shown in the FACS protocol to evaluate the presence of CD45. 2 positive lymphocytes.

Now, we will determine the presence CD45.2 lymphocytes that were isolated from the CD45. 1 host spleen. To start, double click on the FlowJo icon and drag the files for each tube in the all sample window. Then, double click on the transferred file to display the cells recorded from that sample on a dot plot that displays forward scatter FSCA on the x-axis and side scatter SSCA on the y-axis. Click on polygon to circle the lymphocyte populations. A new subpopulation identification window appears. Click on OK. Now, set the y-axis to FSC-W and the x-axis to FSC-A. Select the single cell population with the polygon tool as previously demonstrated.

Next, double click on the circled population to create a new window for the selected cells. In the new window, select CD45.2 on the Y and CD45.1 on the X. Click on the T icon and customize the axis to enlarge the plot. Next, click on polygon to circle the CD45.2 positive cells. In the subpopulation identification window, name your cell population transferred cells and click OK. In the same window, click on rectangle to select the CD45.2 negative cells. In the subpopulation identification window, name your cell population host cells and click OK. Next, double click on the CD45.2 circled population, transferred population, to create a new window for the selected cells. In the new window, select CD3 on the Y and CD4 on the X.

Next, click on polygon to circle the CD4 CD3 positive cells. In this subpopulation identification window, name your cell population transferred CD4 cells. Then, repeat the previous analysis steps with the control mouse file. Finally, to visualize your cell populations, click on Layout Editor. Drag the transferred cells and the transferred CD4 cells population from transferred and control files into the Layout Editor tab. A dot plot representing CD45.2 positive cells and CD4 lymphocytes will appear. CD45. 2 transferred cells should only appear in the transferred mouse dot plot.

Results

Ragγc mice have an altered immune system composition, mainly lacking lymphocytes. Adoptive transfer of splenocytes allows introduction of lacking population such as T and B cells. Our staining included cell surface markers CD45.1 and CD45.2 to distinguish host and donor cells respectively (Figure 2A). It also included other cell surface marker to highlight cell populations absent in Ragγc mice, such as CD4 T cells (Figure 2B). As expected, control mouse did not have CD45.2-positive cells (Figure 2B, top panels) and transferred mouse did (Figure 2B, bottom panels, 71.2% of total cells). We could also specifically detect CD4 T cells within transferred cells (22.1% of CD45.2 cells).

Figure 2
Figure 2: Representative results of adoptive transfer. (A) Histograms of CD45.2 cells from mice injected with PBS (control group) (dashed) and mice injected with CD45.2 splenocytes (test group) (solid line). (B) Gating strategy of CD45.2-positive cells in control mice injected with PBS (top panels) and mice injected with CD45.2 splenocytes (bottom panels). Donor and host cells are distinguished using cell surface markers (CD45.1, CD45.2), then CD45.2-positive cell population are characterized (CD3, CD4). Please click here to view a larger version of this figure.

Applications and Summary

Adoptive transfer is a translational technique in different fields of science, with applications in medicine. This technique can be used to study cell migration and tropism or incidence of protein deficiency in specific cell populations. In the last case, different technologies can be used, especially GMO mice where specific cell populations are intrinsically deficient. However, genetic construction to obtain GMO mice can be a very complex and long process. In this case, adoptive transfer of deficient cell population is easier and faster.

Adoptive transfers have direct applications in medicine. For instance, bone marrow grafts in irradiated patients during cancer therapy are used to reconstitute the immune system. Recently, other applications of adoptive transfer have been used in the medical field. Artificial T cells (called CAR T cell) are designed to recognize and eliminate some cancers. In addition, these engineered cells are built to dampen rejection risk by the host. Transfer of CAR T cells is currently tested in clinical trials.

References

  1. Restifo, N. P., Dudley, M. E. and Rosenberg., S. A. Adoptive immunotherapy for cancer: harnessing the T cell response. Nature reviews. Immunology, 12 (4): 269-281, (2012).
  2. Bonini, C., and Mondino, A. Adoptive T-cell therapy for cancer: The era of engineered T cells. European journal of immunology, 45 (9): 2457-69, (2015).

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 50 mL 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 on the Petri dish containing 5 mL of HBSS 2% FCS.

3. Immune Cell Isolation

  1. Place the spleen on a 40 µm cell strainer over the Petri dish. Crush the spleen with a plunger to dissociate it.
  2. Recover the adhered cells by rinsing the plunger and the strainer with 1 mL of HBSS 2% FCS.
  3. Transfer the dissociated spleen and the fluid into a 15 mL centrifuge tube.
  4. Wash the Petri dish with 5 milliliters of HBSS 2% FCS and transfer the fluid to the 15 mL tube.
  5. Centrifuge the tube at 370 x g for 7 min at 10°C and discard the supernatant avoiding the pellet.
  6. Resuspend the pellet in 2 mL of potassium ammonium chloride pipet up and down to resuspend the pellet and lyse the erythrocytes.
  7. Wait for 2 min and add HBSS 2% FCS to the resuspended pellet to obtain the volume up to 14 mL.
  8. Centrifuge the tube again at 370 x g for 7 min at 10°C. Discard the supernatant and resuspend the pellet in 5 mL of HBSS 2% FCS by pipetting up and down.
  9. Count the cells using trypan blue staining assay and adjust the final cell concentration to 107 cells/mL using appropriate volume of HBSS 2% FCS.

4. Adoptive Transfer

  1. Transfer 2 mL of cell suspension obtained in a 5 mL collection tube.
  2. Centrifuge the tube at 370 x g for 7 min at 10°C and then discard the supernatant.
  3. Resuspend the pellet in 2 mL of PBS and centrifuge the tube at 370 x g for 7 min at 10°C.
  4. Discard supernatant and resuspend pellet in 200 µL of PBS.
  5. Using a 0.5 mL syringe with a 29G needle inject 200 µL of cell suspension into the experimental mouse intravenously into the retro-orbital blood sinus.
  6. As a control, inject a second mouse in the same blood sinus with 200 µL of phosphate buffered saline.

5. Cells Harvest and Staining

  1. Four days after the adoptive transfer, euthanize mice and remove the spleen.
  2. Harvest the splenocytes as described in section 3.
  3. Transfer 100 µL of cell suspensions from each mouse into two FACS tubes, labeled "control" and "transferred".
  4. Centrifuge the tube at 370 x g for 7 min at 10°C and then discard the supernatants.
  5. Prepare a mix containing the four antibodies at the dilutions listed in Table 1.
Antibodies Fluorochrome Dilution
CD45.1 BV711 1/200
CD45.2 APCCy7 1/400
CD4 BV786 1/1600
CD3 BV421 1/200

Table 1: Antibodies mix composition. Four antibodies cocktails preparation using concentrated antibody-fluorescent conjugates and HBSS.

  1. Add 100 µL of the mix to each tube, and then incubate for 20 min on ice in the dark.
  2. Add 1 mL of HBSS 2%FCS and then centrifuge the tubes at 370 x g for 3 min at 10°C.
  3. Discard the supernatants and resuspend the pellets in 200 µL of HBSS 2% FCS.
  4. Transfer the resuspended cells to new, labelled FACS tubes.
  5. Using flow cytometry, as shown in FACS protocol, evaluate the presence of CD45.2 positive lymphocytes.

6. Data Analysis

  1. Open the "FlowJo" software and drag the files for each tube in "All sample" window.
  2. Double click on the "transferred" file to display the cells recorded from that sample on a dot plot that displays forward scatter "SSC-A" on the Y axis and side scatter "FSC-A" on the X axis.
  3. Click on "polygon" and create a gating strategy to select lymphocytes, then distinguish donor and host cells using cell surface markers (CD45.1, CD45.2), and then characterize CD45.2+ cell population (CD3, CD4).
  4. Repeat the analysis steps with "control mouse" file.
  5. To visualize a cell population, click on "Layout editor".
  6. Drag the "transferred cells" and the "transferred CD4 cells" population from "transferred" and "control" files into the "Layout Editor tab".
  7. A dot plot representing CD45.2+ cells and CD4 lymphocytes will appear.
  8. CD45.2 transferred cells should only appear in the "transferred mouse" dot plot.

Adoptive cell transfer is a method for introducing cells of interest into an organism. It is a powerful technique to study various biological mechanisms, including the action of specific classes of immune cells. In addition, adoptive transfer is a promising novel treatment for numerous conditions, such as those requiring bone marrow transplants or cancer treatments where a patient's own T-cells can be extracted, altered to recognize and destroy the cancerous cells, and then returned to the body to fight tumors.

In the laboratory, animal models are often used to study adoptive transfer. For example, CD45.1 Rag gamma-c knockout mice lack fundamental receptors for many cytokines, which are essential for normal differentiation of hematopoietic stem cells into lymphocytes. As a result, the knockout mice have a compromised lymphocyte development and do not have natural killer, or NK, cells, T-cells, or B-cells.

Adoptive transfer can be used to introduce the missing immune cells into these compromised mice, by first harvesting donor mouse tissue containing high concentrations of immune cells, such as the spleen. The tissue is then dissociated and a variety of spleen cells, including the immune cells, are isolated. Next, unwanted erythrocytes, or red blood cells, can be lysed via the addition of ammonium chloride potassium lysing buffer and the remaining white blood cells, or splenocytes, are then separated from the cell debris using centrifugation.

Finally, the purified splenocytes are injected into the immunocompromised mice, facilitating detailed studies of these cells' functions. Several days later, the success of the adoptive immune cell transfer can be confirmed by first isolating and preparing the host splenoncytes in the same manner as the donor tissue. Then, these cells are stained using labeled antibodies against the donor immune cell markers so that they can be verified and sorted using FACS.

To begin, put on laboratory gloves and the appropriate protective equipment. Next, wash a pair of forceps and dissecting scissors first with a detergent and then with 70% ethanol and then dry them with a clean paper towel. Prepare 50 milliliters of Hank's Balanced Salt Solution, or HBSS, with 2% Fetal Calf Serum, or FCS, by combining one milliliter of FCS with 49 milliliters of HBSS in a 50 milliliter tube. Mix by gently pipetting the solution up and down approximately 10 times.

Dissect the euthanized mouse and remove its spleen as demonstrated in the JoVE video protocol FACS technology for splenic B lymphocytes separation. To isolate immune cells, first place the spleen on a 40 micrometer cell strainer in a petri dish. Crush the spleen with a plunger to dissociate it into the dish. Recover the adhered cells by rinsing the plunger and the strainer with 1 milliliter of HBSS 2% FCS. Then, pipette the dissociated spleen and fluid from the petri dish into a 50 milliliter centrifuge tube. Wash the petri dish with 5 milliliters of HBSS 2% FCS and transfer the fluid to the 15 milliliter 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 without disturbing the pellet and discard the liquid in an appropriate waste container. Then, add two milliliters of ammonium chloride potassium lysing buffer to the centrifuge tube and pipette up and down to resuspend the pellet and lyse the erythrocytes. Wait for two minutes and then add HBSS 2% FCS to the resuspended pellet to obtain a total value of 14 milliliters. Repeat the centrifugation. Retrieve the tube carefully and discard the supernatant. Then, resuspend the pellet in 5 milliliters HBSS 2% FCS by pipetting up and down. Next, count the cells in suspension. Add five microliters of trypan blue to five microliters of cell suspension and mix well by pipetting. Then, gently deposit a five microliter drop of diluted cell suspension between the cover glass and the Malassez slide. With the microscope set to 40X magnification, count the number of cells. Adjust the cell concentration to 10 to the seven cells per milliliter by adding the appropriate volume of HBSS 2% FCS.

To begin the adoptive transfer, transfer two milliliters of the cell suspension to a five milliliter collection tube. Centrifuge the tube at 370 times g for seven minutes at 10 degrees Celsius and then discard the supernatant. Next, resuspend the pellet in two milliliters of phosphate buffered saline and centrifuge the tube at 370 times g for seven minutes at 10 degrees Celsius. Discard the supernatant. Then, resuspend the pellet in 200 microliters of phosphate buffered saline. Using a 0.5 milliliter syringe with a 29-gauge needle, inject 200 microliters of cell suspension into the experimental mouse intravenously into the retro-orbital blood sinus.

Four days after the adoptive transfer, euthanize the mice and remove the spleens. Then, harvest the immune cells as described in section three. Next, transfer 100 microliters of cell suspension from each mouse into two FACS tubes labeled control and transferred. Centrifuge the tubes at 370 times g for seven minutes at 10 degrees Celsius and then discard the supernatants. Now, prepare a mix containing the four antibodies at the dilution listed in table one. Add 100 microliters of the mix to each tube and then incubate for 20 minutes on ice in the dark. Next, add one milliliter of HBSS 2% FCS to each tube and then centrifuge the tubes at 370 times g for three minutes at 10 degrees Celsius. Discard the supernatants and then resuspend the pellets in 200 microliters of HBSS 2% FCS. Transfer the resuspended cells to new labeled FACS tubes. Now, use flow cytometry as shown in the FACS protocol to evaluate the presence of CD45. 2 positive lymphocytes.

Now, we will determine the presence CD45.2 lymphocytes that were isolated from the CD45. 1 host spleen. To start, double click on the FlowJo icon and drag the files for each tube in the all sample window. Then, double click on the transferred file to display the cells recorded from that sample on a dot plot that displays forward scatter FSCA on the x-axis and side scatter SSCA on the y-axis. Click on polygon to circle the lymphocyte populations. A new subpopulation identification window appears. Click on OK. Now, set the y-axis to FSC-W and the x-axis to FSC-A. Select the single cell population with the polygon tool as previously demonstrated.

Next, double click on the circled population to create a new window for the selected cells. In the new window, select CD45.2 on the Y and CD45.1 on the X. Click on the T icon and customize the axis to enlarge the plot. Next, click on polygon to circle the CD45.2 positive cells. In the subpopulation identification window, name your cell population transferred cells and click OK. In the same window, click on rectangle to select the CD45.2 negative cells. In the subpopulation identification window, name your cell population host cells and click OK. Next, double click on the CD45.2 circled population, transferred population, to create a new window for the selected cells. In the new window, select CD3 on the Y and CD4 on the X.

Next, click on polygon to circle the CD4 CD3 positive cells. In this subpopulation identification window, name your cell population transferred CD4 cells. Then, repeat the previous analysis steps with the control mouse file. Finally, to visualize your cell populations, click on Layout Editor. Drag the transferred cells and the transferred CD4 cells population from transferred and control files into the Layout Editor tab. A dot plot representing CD45.2 positive cells and CD4 lymphocytes will appear. CD45. 2 transferred cells should only appear in the transferred mouse dot plot.

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