Bioluminescent Monitoring of Graft Survival in an Adoptive Transfer Model of Autoimmune Diabetes in Mice

Summary

This protocol describes a straightforward and minimally invasive method for transplanting and imaging NIT-1 cells in non-obese diabetic (NOD)-severe combined immunodeficient mice challenged with splenocytes purified from spontaneously diabetic NOD mice.

Abstract

Type 1 diabetes is characterized by the autoimmune destruction of the insulin-producing beta cells of the pancreas. A promising treatment for this disease is the transplantation of stem cell-derived beta cells. Genetic modifications, however, may be necessary to protect the transplanted cells from persistent autoimmunity. Diabetic mouse models are a useful tool for the preliminary evaluation of strategies to protect transplanted cells from autoimmune attack. Described here is a minimally invasive method for transplanting and imaging cell grafts in an adoptive transfer model of diabetes in mice. In this protocol, cells from the murine pancreatic beta cell line NIT-1 expressing the firefly luciferase transgene luc2 are transplanted subcutaneously into immunodeficient non-obese diabetic (NOD)-severe combined immunodeficient (scid) mice. These mice are simultaneously injected intravenously with splenocytes from spontaneously diabetic NOD mice to transfer autoimmunity. The grafts are imaged at regular intervals via non-invasive bioluminescent imaging to monitor the cell survival. The survival of mutant cells is compared to that of control cells transplanted into the same mouse.

Introduction

Type 1 diabetes (T1D) is caused by the autoimmune destruction of the insulin-producing beta cells of the pancreas. The loss of beta cell mass results in insulin deficiency and hyperglycemia. T1D patients rely on multiple daily injections of exogenous insulin and experience episodes of severe hyperglycemia and hypoglycemia throughout their lives. The complications related to these episodes include diabetic retinopathy, decreased kidney function, and neuropathy¹.

Insulin injections are a treatment but not a cure for T1D. Replacing the lost beta cell mass, however, has the potential to reverse the disease by enabling patients to produce their own insulin. However, the supply of cadaveric donor islets is limited². Stem cell-derived islets (SC-islets) may provide a virtually unlimited supply of beta cells for transplant. Several groups have demonstrated that human embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) can be differentiated to generate functional beta-like cells^3,4,5. Promising early clinical trial data indicate that these cells maintain their function following transplant and may enable patients to become insulin-independent⁶. Chronic immunosuppression is required, however, thus increasing their susceptibility to cancer and infection. In addition, immunosuppressive agents may be cytotoxic to grafts in the long term⁷. To eliminate the need for immunosuppression, SC-islets may be genetically modified to protect them from recurrent autoimmunity as well as alloimmunity after transplant.

Stem cell research is highly demanding in costs and labor. Mouse cell lines and animal models are useful tools for the initial identification and experimental validation of strategies to protect transplanted cells from autoimmunity. The NOD mouse develops spontaneous autoimmune diabetes with many similarities to human T1D⁸, and the NIT-1 insulinoma cell line shares a genetic background with this mouse strain⁹. Diabetes can be adoptively transferred to the related immunodeficient NOD-scid mouse strain via the injection of diabetic splenocytes from NOD mice in order to temporally synchronize the onset of diabetes in replicate experimental mice¹⁰. This model can be used to identify genetic targets relatively quickly and inexpensively for further validation in SC-islets. Recently, the method was applied to identify and validate RNLS, a target that was found to protect primary human islets from autoimmunity in vivo and iPSC-derived islets from beta cell stress in vitro¹¹. Described here is a straightforward protocol to transplant genetically engineered NIT-1 cells and non-invasively monitor their survival in an adoptive transfer model of autoimmune diabetes in mice.

Protocol

Figure 1: The workflow for transplanting and imaging grafts in an adoptive transfer model of diabetes in mice. NIT-1 cells expressing the firefly transgene luciferase (luc2) are transplanted subcutaneously into NOD-scid mice. The mice are simultaneously injected with autoreactive splenocytes isolated from a spontaneously diabetic NOD mouse. The grafts are imaged at regular intervals by non-invasive bioluminescent imaging. Figure created by BioRender.com. Abbreviations: NOD = non-obese diabetic; scid = severe combined immunodeficient. Please click here to view a larger version of this figure.

All animal care and study protocols were approved by and performed in accordance with the Institutional Animal Care and Use Committee (IACUC) at the Joslin Diabetes Center. NOD and NOD-scid mice may be readily obtained from commercial sources. All mice in this study are maintained in a sentinal-monitored facility. See the Table of Materials for details related to all the materials, animals, instruments, and software used in this protocol.

1. Engineering and maintenance of NIT-1 cell lines

1. Maintain NIT-1 cell lines, which share a genetic background with NOD mice, and 293FT cells in tissue culture-treated dishes in DMEM containing 4.5 g/L glucose supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin in a 37 °C incubator with 5% CO₂.
2. Grow the 293FT cells to 70%-80% confluence for transfection.
3. Per 10 cm dish of 293FT cells, combine 10 µg of pLenti-luciferase-blast (see Supplemental File 1), which expresses the firefly luciferase transgene (luc2) under the control of the constitutively active EF1α promotor, 2 µg each of the packaging plasmids pMD2.G, pMDLg/pRRE, and pRSV-Rev, 4 µg of the envelope protein plasmid pCMV-VSV-G, and 60 µg of linear polyethylenimine (PEI) in 1 mL of serum-free DMEM. Adjust the amounts based on the number of cells to be transfected.
4. Leave the DNA, PEI, and DMEM at room temperature (RT) for 20 min, and then add them to the 293FT cells.
5. Collect the medium containing the lentiviral particles 48 h post transfection.
6. Transduce the NIT-1 cells at ~80% confluency with 1 mL of medium containing lentiviral particles per 10⁶ cells for 48-72 h.
7. Select the luciferase-expressing cells with 5 µg/mL blasticidin for 48 h.
8. Further genetically modify the luciferase-expressing cells to suit the experimental question. Include a luciferase-expressing wild-type or non-targeting control cell line for comparison.
   NOTE: Examples of target gene modifications include CRISPR knockout, CRISPRa/i, shRNA knockdown, and overexpression.

2. Preparation of NIT-1 cells for transplant

1. Grow the luciferase-expressing cells until they are 80%-90% confluent.
2. Remove the growth medium and wash the cells with phosphate-buffered saline (PBS, 5 mL for a 10 cm dish).
3. Add 1 mL of 0.05% trypsin-EDTA to each dish for 2 min.
4. Neutralize the trypsin with 5 mL of growth medium.
5. Use a pipette to wash the cells off the dish and transfer them to a conical tube.
   NOTE: Cells from multiple dishes of the same cell line can be combined.
6. Count the cells using a stain such as trypan blue manually with a hemocytometer or automatically with an automatic cell counter.
7. Centrifuge at 250 × g for 5 min at RT and remove the supernatant with an aspirating pipette.
8. Resuspend the cell pellet in PBS at a concentration of 5 × 10⁷ cells/mL (10⁷ cells per cell line per mouse will be transplanted in a volume of 200 µL).
9. Keep the cells on ice (for up to 3 h) until transplantation.

3. Transplantation of NIT-1 cells into NOD-scid mice

1. Anesthetize the recipient mice (8-10-week-old NOD-scid mice of the same sex as the mice used to isolate the splenocytes) by isoflurane inhalation in a knockdown chamber. Deliver 2.5% isoflurane into the chamber at a flow rate of 1.5 L/min and an evacuation rate of 9 L/min. 
2. Lubricate the animal's eyes with ophthalmic ointment to prevent drying.
3. Using an electric shaver with a guard, remove the hair from the back (dorsal side) of the mice to expose the skin. The shaved transplant area will be approximately 1 in x 2 in. Return the shaved mice to the knockdown chamber until the transplant.
4. Transfer the mice one at a time to a clean surface with an isoflurane nose cone. Gently guide the mouse's head into the nose cone. Use an isoflurane flow rate of 0.25 L/min to maintain the anesthesia during the transplant.
5. Wipe the transplant area with an isopropyl alcohol prep pad to remove loose hair and disinfect the skin.
6. Ensure the cells are fully resuspended before loading the syringe. Draw an excess volume (>300 µL) of cells into a 1 mL sterile syringe with a 26 G needle. Remove any bubbles; then, return excess cells to the tube so that 300 µL of cell suspension remains in the syringe.
7. Using a pair of curved forceps held in the non-dominant hand, gently lift the skin on one side (left or right) of the mouse's back to allow for easier access to the subcutaneous space.
8. Using the dominant hand, position the syringe parallel to the coronal and sagittal planes of the mouse's body. With the needle pointed toward the head of the mouse, insert the needle into the skin near the hindquarters, and gently guide it into the subcutaneous space. Ensure that the entire needle remains under the skin and does not poke through.
9. Adjust the forceps to gently hold the skin around the base of the needle. Slowly dispense a small amount of cell suspension (<50 µL) and confirm that a small bulge forms under the skin at the site of the injection. Continue injecting the cell suspension until 200 µL has been delivered to the subcutaneous space.
10. Holding the forceps in place and keeping the needle parallel to the mouse's body, slowly withdraw the needle. After the needle has been removed, hold the skin closed with forceps for a few seconds to prevent the cells from leaking out of the puncture wound.
11. If a genetic modification is being evaluated, repeat the transplant on the opposite side of the mouse using a different syringe so that both mutant and control cells are injected into each mouse, with one cell line on the left and the other on the right. If only one cell line is being transplanted, inject the cells on one side only.
12. Following the transplant, transfer each mouse to a fresh cage. Allow each mouse to fully recover from the anesthesia before adding additional mice to the cage.
    NOTE: Mice are recovered when they resume normal activities and do not show signs of lethargy or impaired movement.
13. Evaluate the health status of the mice daily for the duration of the experiment following the transplant. If the grafts form a large bulge or the mice become weak and lethargic, measure their blood glucose and provide 10% (w/w) sucrose water ad libitum to all the hypoglycemic mice. Follow all veterinary recommendations and euthanize any mice with continued poor body condition as per institutional guidelines. In this study, mice were euthanized by CO₂ inhalation followed by cervical dislocation.

4. Isolation and purification of autoreactive splenocytes

1. Identify 10-16-week-old male or female NOD mice with recent-onset (less than 10 days) diabetes by using urine (or blood) glucose test strips. NOD mice are considered diabetic when they have urine/blood glucose ≥250 mg/dL on at least 2 consecutive days.
   NOTE: For each NOD-scid mouse, 10 million splenocytes are needed; one spleen typically yields 50 million to 150 million splenocytes. The splenocytes were isolated from pathogen-free mice housed in a sentinal-monitored facility.
2. Euthanize the appropriate number of diabetic NOD mice.
   NOTE: In this study, the mice were euthanized by CO₂ inhalation followed by cervical dislocation to ensure death.
3. With the mouse on its back, make a vertical incision approximately 2 in in length in the skin with surgical scissors. Open the right side of the mouse from the researcher's point of view and locate the bright red spleen. Gently cut the spleen away from the pink pancreas and transfer it to a sterile 10 cm Petri dish containing 5 mL of sterile PBS. Repeat the dissection with as many mice as needed.
   NOTE: Spleens from multiple mice can be combined in one dish. Conduct the following steps using sterile reagents and equipment in a sterile hood.
4. Mash the spleen(s) with the flat top of a sterile syringe plunger.
5. Place a 40 µm or 70 µm strainer in a 50 mL conical tube and wash the strainer with 5 mL of PBS to prime it. Transfer the spleen(s) suspension into the strainer and continue gentle mashing through the strainer. Wash the dish with 10 mL of PBS and transfer the wash to the strainer. Continue mashing until the red color is gone from the strainer.
6. Discard the strainer and spin the tube at 500 × g for 5 min at RT. Remove the supernatant with an aspirating pipette.
7. Resuspend the cell pellet in 5 mL (for up to three spleens) of ACK lysis buffer prewarmed to RT and lyse the red blood cells for 4 min. Increase the volume by 1-2 mL per spleen if additional spleens are needed.
8. Stop the reaction with 5 mL of NIT-1 cell media (described above) per 5 mL of lysis buffer. Pass the cell suspension through a fresh strainer to remove clumps. Discard the strainer, and spin at 500 × g for 5 min at RT.
9. Resuspend the cell pellet in 20 mL of PBS, and count the cells. Spin at 500 × g for 5 min at RT. Resuspend the cells in sterile PBS at a concentration of 1 × 10⁸ cells/mL (the injection volume is 0.1 mL/mouse) in a 1.5 mL safe-lock reaction tube.
10. Store the cells on ice (for not more than 1 h) or keep the cells at RT, and proceed to the tail vein injection immediately.

5. Intravenous injection of diabetic splenocytes via the lateral tail vein

1. Warm up the body of the adult recipient NOD-scid mice (e.g., by using a heat lamp for ~5-10 min) to vasodilate the veins (this helps for visualization and injection into the vein).
   NOTE: To avoid the overheating of the mice, do not exceed this time. Always monitor the health status. If the mice appear exhausted or immobile, shut off the heat lamp immediately.
2. Warm up the cell suspension. Prepare a sterile syringe (0.3-1.0 mL) with a sterile needle (27-30 G, 0.3 mm/0.5 in or smaller), or use a sterile 0.5 mL insulin syringe with a 0.3 mm (0.5 in) needle. Always keep the needle sterile and use a sterile tray if the syringe must be put down between injections.
3. Resuspend the splenocyte solution prior to each injection. For each mouse, draw 100 µL of the prewarmed and mixed splenocyte suspension into the syringe. Make sure that no air bubbles are present in the syringe or in the suspension.
   NOTE: Make sure to have all the equipment and supplies prepared (alcohol wipes for disinfection, a syringe loaded with the splenocytes to be injected, and a fresh cage for separating injected mice) before placing the mouse in the restraint device.
4. Place the mouse in the restraint device. Capture the tail with the non-dominant hand and locate one of the two lateral tail veins. Gently rotate the tail if needed. Wipe the tail with a disinfection wipe (70% isopropyl alcohol) to clean the skin and increase the visibility of the vein.
5. Insert the needle at an acute angle into the central region of the tail with the dominant hand. With the bevel of the needle facing up, slide the needle a few millimeters through the skin.
   NOTE: Make sure the needle is parallel to the vein and placed just slightly under the skin. Be prepared for sudden movements of the mouse/tail directly after penetrating the skin/vessel wall. A successful insertion of the needle should feel like a "smooth slide" into the vein. If another attempt is needed, move further up the tail toward the body.
6. Apply gentle pressure to the syringe to inject the splenocyte suspension. Do not allow the needle to move further in or out when injecting. Successful injections are smooth without feeling any back pressure during injection and are indicated by a transparent/white blood flow immediately following injection.
7. Gently release the needle out of the vein, and apply light pressure to the tail with a disinfection wipe until the bleeding stops. Release the mouse from the restraint device, and gently transfer it to a freshly prepared cage.
   NOTE: Inject two to three control mice that do not receive a NIT-1 cell transplant with splenocytes to confirm the potential of the autoreactive splenocytes to induce diabetes, which takes approximately 2-4 weeks post injection.

6. In vivo bioluminescent imaging of NIT-1 grafts

NOTE: Image the grafts one to two times per week. On the day of the transplant, wait at least 2 h after the transplant to allow the grafts to settle and ensure stable luciferase expression. If time is a limiting factor, the initial measurement may be taken on Day 1 instead. A recommended initial imaging schedule is Day 0 or Day 1 post injection, Day 5, Day 10, Day 14, Day 18, and Day 25. Adjust the schedule, however, based on the progress of autoimmunity as judged by the loss of bioluminescent signal.

1. Prepare a 15 mg/mL D-luciferin solution in Dulbecco's PBS. Agitate at RT to dissolve, and sterile-filter (0.22 µm). Store 1 mL aliquots at −20 °C, and thaw as needed.
   NOTE: The aliquots can be refrozen.
2. At least 5 min prior to imaging, inject the mice intraperitoneally using a 1 mL syringe and a 26 G needle with D-luciferin solution at a dose of 150 mg/kg. 
   NOTE: Use a fresh syringe and needle for each mouse. 
3. Anesthetize the mice by isoflurane inhalation according to institutional guidelines. The recommended conditions are 2.5% isoflurane with a flow rate of 1.5 L/min into the knockdown chamber and an evacuation rate of 9 L/min.
4. Lubricate the animal's eyes with ophthalmic ointment to prevent drying.
5. Open the software associated with the imaging instrument. Create a new user and/or login. On the control panel on the bottom right, select Initialize (Figure 2A). To auto-save the imaging data, create the appropriate folders on the computer, and then select Acquisition | Auto-save to… (Figure 2A). Once the instrument has finished initializing, set the exposure time to 1 min.
   NOTE: The complete imaging parameters are shown in Figure 2B.
6. Transfer the mice one at a time from the knockdown chamber to the imaging instrument. Place the mouse on its stomach with its limbs splayed, and gently guide its head into the nose cone. An isoflurane flow rate of 0.25 L/min delivered via a nose cone is appropriate to maintain anesthesia during imaging. Gently flatten the mouse by pressing the center of its back with both hands and then spreading the hands outward and apart.
7. Select Acquire (Figure 2B). Record any relevant details of the experiment in the pop-up window (Figure 2C).
   NOTE: See Figure 3A for representative images of three 8-week-old female NOD-scid mice transplanted with two grafts at various time points.

Figure 2: Screenshots of the software commands for imaging bioluminescent grafts. (A) Prior to imaging, select Initialize to prepare the instrument. The images may be auto-saved to a folder of choice by selecting Acquisition | Auto-save to… (B) Overview of the imaging parameters. Once the mouse has been positioned in the instrument, select Acquire. (C) Screenshot of the dialog box that pops up during imaging. Details such as the time point and mouse strain may be entered here. Please click here to view a larger version of this figure.

7. Data analysis

1. Quantify the bioluminescent signal at any time after imaging. Open the software associated with the imaging instrument. Select File | Open, and select the ClickInfo.txt file associated with the mouse to be analyzed.
2. In the Tool Palette, select ROI Tools (Figure 3B, Step 1). From the oval dropdown menu (Figure 3B, Step 1, red arrow), select the number of grafts that were transplanted into the mouse.
3. Move the ovals so that they contain the bioluminescent signal from each graft, and select Measure ROIs (Figure 3B, Step 2).
4. Record the Total Count for each graft (Figure 3B, Step 3).
5. For each graft, divide the bioluminescent signal measured at every time point by the signal measured at the first time point. Report the graft survival as the proportion or percentage of residual bioluminescent signal relative to the initial bioluminescent signal.
   NOTE: If the grafts expand post transplant, the ratio or percentage of graft survival will be greater than 1 or 100%, respectively. All the mice that receive transplants should be monitored for adverse health effects.

Representative Results

An overview of the protocol is outlined in Figure 1. The survival of two cell lines, such as a mutant and a non-targeting control, may be compared, or the survival of one cell line may be measured in multiple groups of mice, such as drug-treated mice versus vehicle-treated controls. Figure 3A shows three 8-week-old female NOD-scid mice transplanted with a non-targeting control (left) and a mutant (right) cell line. The mice were also injected intravenously with autoreactive splenocytes to transfer diabetes.

The mice were imaged on Day 0, Day 5, Day 10, Day 14, and Day 18 post injection. In two out of the three mice, the control graft was destroyed by Day 18, as evidenced by the loss of bioluminescent signal, while the mutant graft was protected. In one mouse, the mutant graft but not the control graft was destroyed, highlighting the biological variation between animals. The bioluminescent signal was quantified as described in Figure 3B. The graft survival is reported as the percentage of residual bioluminescent signal compared to the first time point (Figure 3C). It is also useful to calculate the ratio of mutant to control luminescent signals for each mouse to visualize the variation between animals (Figure 3D). At the end of the data collection period, the mice were euthanized by CO₂ inhalation followed by cervical dislocation.

Prior to disease transfer, the transplanted cells may replicate, resulting in expanded grafts that are visible through the skin (Figure 4A). These grafts will have saturated bioluminescent signals when imaged (Figure 4B), which may not be accurately quantified.

Figure 3: Representative images and quantification of the bioluminescent signal. (A) Three 8-week-old female NOD-scid mice were transplanted with non-targeting control (right) and mutant cells (left) and intravenously injected with autoreactive splenocytes to induce diabetes. The mice were non-invasively imaged on Day 0, Day 5, Day 10, Day 14, and Day 18 post injection. The bioluminescent signal is illustrated by a color spectrum ranging from low intensity (blue) to high intensity (red). (B) Instructions for quantifying the bioluminescent signal. (C) Average percentage of graft luminescence remaining over time. (D) Ratio of the percentages of graft luminescence over time for mutant versus non-targeting control grafts for each mouse. Ratio = 1 indicates time points at which the percentage of signal remaining is equal for both grafts. Abbreviations: NOD = non-obese diabetic; scid = severe combined immunodeficient; NTC = non-targeting control; Mut = mutant. Please click here to view a larger version of this figure.

Figure 4: Examples of grafts that are excessively expanded. (A) Expanded grafts may bulge through the skin of the mouse (indicated by the red arrow). (B) Expanded grafts may yield saturated bioluminescent signals. The bioluminescent signal is illustrated by a color spectrum ranging from low intensity (blue) to high intensity (red). Please click here to view a larger version of this figure.

Supplemental File 1: pLenti-luciferase-blast sequence. Please click here to download this File.

Discussion

T1D is a devastating disease for which no cure currently exists. Beta cell replacement therapy offers a promising treatment for patients with this disease, but the critical barrier to this strategy is the potential for recurrent autoimmune attack against the transplanted beta cells. The genetic engineering of SC-beta cells to reduce their immune visibility or susceptibility is one potential solution to this problem. Described here is a protocol for non-invasively imaging transplanted beta cells to measure their survival in an adoptive transfer model of autoimmune diabetes in mice.

A key advantage of this method is the adaptability of the protocol. The method is applied here to compare a mutant cell line to a non-targeting control (Figure 3), but the protocol can accommodate a variety of experimental questions. The protective effects of a wide range of genetic modifications, drugs, or other treatments against autoimmune attack could be explored. When evaluating the efficacy of a drug or other treatment in protecting against autoimmunity, only cells expressing luciferase with no additional genetic modifications are needed. While syngeneic transplants to test autoimmune protection are used in this paper, the method may be also be adapted to evaluate alloimmune rejection by using a combination of a cell line and a mouse strain that are not syngeneic, such as NIT-1 cells and C57BL/6J mice. The protocol may also be modified to explore immune infiltration into the grafts. Additional mice from which grafts are retrieved at various time points may be included, and the infiltrating immune cells may be profiled by immunohistochemistry or flow cytometry.

A major limitation of the application of this method is the failure of the results obtained in mice to translate to human cells and patients. Over 500 strategies for autoimmune protection have been implemented with success in diabetic mouse models, yet the majority have failed to demonstrate clinical benefit⁷. Primary human islets are a limited resource, however, and stem cell work has high financial and labor costs. The protocol described here is a tool for the preliminary identification of potential therapeutic targets utilizing a relatively inexpensive and simple mouse technique. Subsequent experiments should be performed with primary and/or SC-islets, which are typically transplanted under the kidney capsule in mice. The method described here can be adapted to evaluate the efficacy of therapeutic strategies in human cells. Both primary and SC-islets can be engineered to express luciferase, and their survival can be measured by bioluminescent imaging following transplant under the kidney capsule into humanized mouse models^12,13. Methods for non-invasively monitoring the survival of islet grafts transplanted onto the iris of the eye by confocal microscopy have been also been reported¹⁴.

An additional limitation associated with the method described in this paper is the variation in the autoreactive potential of isolated splenocytes. Although the rate of disease transfer is high¹⁰, the timeline of diabetes onset post splenocyte injection can vary from 2 weeks to 4 weeks. During this time, the transplanted cells can expand (Figure 4), resulting in hyperinsulinemia and severe hypoglycemia. Combining splenocytes from multiple diabetic donor mice can reduce the variation between experiments.

Despite these limitations, the method is a straightforward and informative tool for testing strategies for autoimmune protection. The protocol utilizes basic cloning and cell culture techniques, a simple and minimally invasive mouse surgery, and non-invasive imaging, allowing the user to maximize the data collection while minimizing the number of animals needed per experiment. As an alternative to in vivo bioluminescent imaging, grafts may be recovered at various time points, weighed, photographed, and further processed for immune cell characterization. This strategy requires larger numbers of mice, as graft recovery requires euthanasia, and it is desirable to have replicates at each time point. In addition, the graft retrieval method allows for only one size measurement to be taken per graft. As the timeline of beta cell killing by autoreactive splenocytes varies across individuals, it can be difficult to determine the optimal time point for graft recovery. The approach described in this paper allows the researcher to monitor the progress of autoimmunity in live mice and obtain a complete timeline of graft destruction. As long as mice maintain euglycemia, protected grafts can be left in the mice and imaged over long periods of time to elucidate the degree of protection.

Described here is a straightforward protocol for transplanting and non-invasively imaging beta cell grafts in an adoptive transfer mouse model of autoimmune diabetes. This method enables a minimal number of animals to be used and allows flexibility in the timing of graft analysis, which is critical given the variation in the progress of autoimmunity. The protocol can also be readily adapted to address a wide range of experimental questions. Mouse models are critical in the discovery and validation of new therapeutic strategies, and this method is a valuable tool for advancing the beta cell replacement therapy field.

Materials

Name	Company	Catalog Number	Comments
0.05% Trypsin, 0.53 mM EDTA	Corning	25-052-CI
293FT	Invitrogen	R70007	Fast-growing, highly transfectable clonal isolate derived from human embryonal kidney cells transformed with the SV40 large T antigen
ACK Lysing Buffer	Gibco	A10492-01
Alcohol prep pads, 70% Isopropyl alcohol	Amazon/Ever Ready First Aid	B08NWF31DX
BD 5ml Syringe Luer-Lok Tip	BD	309646
BD PrecisionGlide Needle 26G x 5/8 (0.45 mm x 16 mm) Sub-Q	BD	305115
BD 1 mL TB Syringe Slip Tip	BD	309659
Blasticidin S HCl	Corning	30-100-RB
Cell strainer premium SureStrain, 70 µm, sterile	Southern Labware	C4070	Or use similar sterile strainer with 40-70um pore size
CellDrop automated cell counter	Denovix	CellDrop BF-PAYG	Or use similar cell counter device
Corning 100 mL Penicillin-Streptomycin Solution, 100x	Corning	30-002-CI
Disposable Aspirating Pipets, Polystyrene, Sterile, Capacity=2 mL	VWR	414004-265	Or use similar aspirating pipette
D-Luciferin, Potassium Salt , Molecular Biology Grade, Powder, >99%	Goldbio	LUCK-100
DMEM, high glucose, pyruvate, no glutamine	Gibco	10313039
Falcon BD tubes, 50 mL	Fisher Scientific	14-959-49A
Fetal Bovine Serum	Gibco	10437-028
Forceps premium for tissues, 1 x 2 teeth 5 in, German Steel	Fisher Scientific	13-820-074
Glucose urine test strip	California Pet Pharmacy	u-tsg100	Or use similar test strip for glucose measurments in urine/blood
GlutaMAX–1 (100x)	Gibco	35050-061
Infrared heating lamp	Cole Parmer	03057-00	Or use similar infrared lamp
Insulin syringe 0.5 mL, U-100 29 G 0.5 in	Becton Dickinson	309306
Isoflurane, USP	Piramal Critical Care	6679401725
IVIS Spectrum in vivo imaging system	Perkin Elmer	124262	Instrument for non-invasively collecting bioluminescent images of transplanted cells
Living Image Analysis Software	Perkin Elmer	128113	Software for collecting and quantifying bioluminescent signal
Microcentrifuge tubes seal-rite, 1.5 mL	USA Scientific	1615-5510	Or use similar sterile microcentrifuge tubes
NIT-1	ATCC	CRL-2055	Pancreatic beta-celll line derived from NOD/Lt mice
NOD.Cg-Prkdcscid/J	The Jackson Laboratory	001303	Mice homozygous for the severe combined immune deficiency spontaneous mutation Prkdcscid, commonly referred to as scid, are characterized by an absence of functional T cells and B cells, lymphopenia, hypogammaglobulinemia, and a normal hematopoietic microenvironment.
NOD/ShiLtJ	The Jackson Laboratory	001976	The NOD/ShiLtJ strain of mice (commonly called NOD) is a polygenic model for autoimmune type 1 diabetes
PBS, pH 7.4	Thermo Fisher Scientific	10010031	No calcium, no magnesium, no phenol red
pCMV-VSV-G	Addgene	8454
pLenti-luciferase-blast	Made in-house	Plasmid available upon request	See Supplemental File 1
pMD2.G	Addgene	12259
pMDLg/pRRE	Addgene	12251
Polyethylenimine, Linear, MW 25,000, Transfection Grade (PEI 25K)	Fisher Scientific	NC1014320
pRSV-Rev	Addgene	12253
Restrainer for rodents, broome-style round 1 in	Fisher Scientific	01-288-32A
Scissors, sharp-pointed	Fisher Scientific	08-940	Or use other scissors made of surgical-grade stainless steel
Tissue-culture treated culture dishes	Millipore Sigma	CLS430167-20EA	Or use other sterile cell culture-treated Petri dishes
Tweezers/Forceps, fine precision medium tipped	Fisher Scientific	12-000-157