Mouse Kidney Transplantation: Models of Allograft Rejection

Summary

Here, we present a protocol to study the immunology of rejection. The surgical model presented reports a short operating time and a concise technique. Depending on the donor-recipient strain combination, the transplanted kidney may develop acute cellular rejection or chronic allograft damage, defined by interstitial fibrosis and tubular atrophy.

Abstract

Rejection of the transplanted kidney in humans is still a major cause of morbidity and mortality. The mouse model of renal transplantation closely replicates both the technical and pathological processes that occur in human renal transplantation. Although mouse models of allogeneic rejection in organs other than the kidney exist, and are more technically feasible, there is evidence that different organs elicit disparate rejection modes and dynamics, for instance the time course of rejection in cardiac and renal allograft differs significantly in certain strain combinations. This model is an attractive tool for many reasons despite its technical challenges. As inbred mouse strain haplotypes are well characterized it is possible to choose donor and recipient combinations to model acute allograft rejection by transplanting across MHC class I and II loci. Conversely by transplanting between strains with similar haplotypes a chronic process can be elicited were the allograft kidney develops interstitial fibrosis and tubular atrophy. We have modified the surgical technique to reduce operating time and improve ease of surgery, however a learning curve still needs to be overcome in order to faithfully replicate the model. This study will provide key points in the surgical procedure and aid the process of establishing this technique.

Introduction

Successful renal transplantation for the treatment of renal failure was first described in 1955 between monozygotic twins¹, since then it has become a revolutionary treatment for patients with end-stage renal failure throughout the world, offering both improvement in length and quality of life². However long term graft survival has been hampered by a multitude of pathological processes resulting in chronic allograft damage³.

Rejection of the transplanted kidney in humans remains a major cause of morbidity, despite significant improvements in immunosupporessive regimens. The aim of developing a mouse model of renal transplantation is to closely replicate the process and pathology found in human renal transplantation⁴. Skoskiewicz et al. first described the mouse model of renal transplantation in 1973⁵. Although advanced microsurgical skills are required, it is a valuable tool for several reasons: the mouse genome has been well characterized and there is a great variety of experimental methods and techniques available for mouse studies.

Many groups using the mouse model of renal transplantation have used the transplanted kidney as a life-supporting organ, however in other studies and in our described methodology one of the recipient mouse’s native kidneys is left in situ for the duration of the experiment⁴. The benefit is that the mouse undergoes a single anesthesia and operation thereby reducing the morbidity to the mouse and the risk of death from a second procedure. Additionally the mouse does not suffer from the adverse effects of gradual renal failure.

Although models of allogeneic rejection exist in other organs such as the heart and skin, these are not always directly relevant to renal transplantation. There is evidence that these models elicit different modes and dynamics of rejection, for instance the time course of rejection in cardiac allograft and renal allograft differs significantly in certain strain combinations⁶. We have described acute renal allograft rejection patterns in BALB/c donors into non-transgenic FVB/nj mice, this model showed cellular mediated injury with accumulation of T cells and macrophages⁷. Alternatively we have also described a model of chronic allograft damage that exhibits interstitial fibrosis and tubular atrophy, this results from transplanting a kidney from C57BL/6^BM12 donors into C57BL/6 recipients, as these mice are characterized by a single MHC class II loci mis-match⁸.

Multiple aspects of transplantation have been studied using the mouse model of renal transplantation including acute rejection, cellular and humoral rejection, ischemia reperfusion injury, and trialing novel therapeutic agents. We have modified the surgical technique to reduce operating time and improve the ease of surgery. Particularly we have described simultaneous donor and recipient preparation and a simplified vascular anastomosis technique by utilizing a continuous aortic patch anastomosis. This video and manuscript will provide key points to aid in the establishment of this technique.

Protocol

Appropriate national and local institutional ethics should be in place before performing animal experiments. Specifically in the United Kingdom the following experiments were undertaken under the Animals (Scientific Procedures) Act 1986. Where two microsurgeons are available to operate simultaneously the donor surgeon should perform steps 1.1 to 1.16 then 3.1 to 3.5, whilst the recipient surgeon performs 2.1 to 2.8. For a single operator the steps can be followed sequentially.

1. Donor Preparation

Note: The procedure presented here is for a donor C57BL/6^BM12 and recipient C57BL/6 male mice aged between 8 to 16 weeks old with a body weight greater than 20 g. However this procedure can be reproducibly performed on a variety of mouse strains. The data presented in the representative results section was obtained from C57BL/6, C57BL/6^BM12 and BALB/c mice.

1. Conduct procedures using sterile surgical instruments and consumables (autoclaved), with endeavors to keep the operating area as sterile as possible. Perform the donor preparation simultaneously with the recipient preparation if two surgeons are available.
2. Anesthetize the mouse with an intraperitoneal injection (31G needle) of medetomidine (0.5 mg/kg) and ketamine hydrochloride (200 mg/kg). This results in an anesthetic plane that is maintained for 4 hr providing enough time for the whole procedure to be performed. Supplemental anesthesia is not necessary.
3. Confirm that the mouse is anaesthetized (no response to toe pinch).
4. Shave the mouse’s abdomen and remove any loose hair with sticky tape.
5. Place the mouse on its back on a sterilely draped heated mat and loosely immobilize the limbs with sterile masking tape.
6. Monitor the mouse throughout the procedure for thermal burns. If possible use a non-electric heat source.
7. Apply an eye lubricant and sanitize the abdominal wall with a dilute iodine solution.
8. Make a midline incision in the abdomen to enter the peritoneal cavity and insert a 3 cm Calibri abdominal retractor.
9. Apply warmed saline to keep the intestines and surgical area moist and avoid unnecessary drying of the viscera.
10. Cover the mouse with sterile drapes and move the intestines to the operator’s left (mouse’s right) to expose the aorta, vena cava and left kidney.
11. Apply a ratcheted forcep to the stomach and pull superiorly to expose the major vessels and left kidney fully. Pack damp sterile swabs (2 mm x 2 mm) into the abdomen to retract tissues away from the surgical area, such as the liver lobes, seminal vesicles, and bowel.
12. Isolate the left kidney from surrounding adventia, fat and the left adrenal gland in the peritoneal cavity by bluntly dissecting the connective tissue using fine tip forceps. Place the closed tips of the forceps between the areas that need to be separated and slowly allow the forcep tips to open to dissect the space.
13. Isolate the left renal vein by ligating and then dividing the left adrenal vein and left gonadal vein with 9/O nylon. Place the suture close to the renal vein.
14. Ligate and divide the ureter with 7/O silk suture close to the bladder leaving the suture ends long. These long suture ends will be used when the kidney is harvested and are necessary for the ureteric anastomosis.
15. To mobilize and fully dissect the aorta and vena cava superiorly and inferior to the renal artery and vein use fine tip forceps to bluntly dissect lymphatic vessels and fat from the front and sides of the vessels.
16. Find the tissue plane between the aorta and vena cava and slowly spread the forceps. Slowly open the tips of the fine tipped forceps to spread the tissue with minimal trauma.
17. Tie a loose 7/O silk around the aorta superior and inferior to the renal artery by passing an angled fine tip forceps around the back of the vessels and drawing a suture through. These sutures will be tightened prior to kidney retrieval to allow retrograde perfusion of University of Wisconsin solution.

2. Recipient Preparation

As per the donor preparation follow steps 1.2 to 1.8.

1. Move the intestines to the operator’s right (mouse’s left) to expose the aorta, vena cava. Cover the intestines with a sterile saline soaked swab.
2. Perform a right nephrectomy by ligating the right renal artery and vein together with 7/0 silk suture and then divide.
3. Ligate the right ureter with 7/O silk suture and divide.
4. Mobilize and fully dissect the aorta and vena cava inferior to the renal artery and vein as described in step 1.14 and 1.15. Ensure complete dissection between the aorta and vena cava. Take care to preserve the internal spermatic artery which runs anterior to the vena cava and aorta along with the lymphatic bundle.
5. Identify lumbar vessels running in the retroperitoneum from the vena cava and vein to the spine, ligate with 9/O silk in continuity, there is no need to divide the vessels.
6. Identify sufficient space to place microvascular clamps with space between for vascular anastomoses.
7. Administer intravenous heparin (5 units) via dorsal penile vein.

3. Donor Kidney Retrieval

Tighten the 7/O silk ties that have been placed around the inferior and superior aorta to isolate the kidney from the arterial circulation.

1. Infuse retrograde cold 0.2 – 0.5 ml of University of Wisconsin solution with a needle (31G) into the aorta.
2. Divide the aorta within the sutures and divide the renal vein at its junction with the vena cava to remove the kidney and the renal artery with a length of aorta. Divide lumbar vessels arising from the aorta, if they are present, without ligation.
3. Place the kidney in cold saline on a sterile swab in a culture dish.
4. Euthanize the donor mouse by cervical dislocation.

4. Kidney Transplantation – Kidney Preparation

1. Create an aortic patch by dividing the aorta wall longitudinally directly opposite the renal artery. Identify any vessel lumens in the patch that need to be ligated or avoided when performing the arterial anastomosis.
2. Place a 10/O suture from outside to inside the renal vein lumen superiorly and a second separate suture inferiorly. The sutures used to divide the adrenal vein and gonadal vein can be used to orientate the vessel.
3. Place the kidney in the right flank of the recipient (Figure 1.1) and ensure the sutures are well placed to ensure vascular anastomoses can be completed without the sutures becoming entwined in swabs or other instruments.

5. Kidney Transplantation – Vascular Anastomosis

Apply microvascular clamps first inferiorly then superiorly encompassing the vena cava and aorta.

1. Make a ventomy with a needle (31G) by puncturing the anterior wall of the vena cava. Flush blood from the vena cava by injecting approximately 50 μl of 0.9% NaCl.
2. Widen the venotomy using fine tip forceps by opening them within the venotomy so that the length is equivalent to the diameter of the donor renal vein.
3. Place the 10/O superior suture (which is already in the lumen of the renal vein) first at the apex of the venotomy (Figure 1.2) and join the back wall of the anastomosis in a running suture until the inferior apex is reached (Figure 1.3).
4. Place the 10/O inferior suture and tie first with a single knot (Figure 1.4) then tie to the running suture from the back wall.
5. Using the inferior suture create the front wall of the anastomosis (Figure 1.5) with a running suture and tie to the superior suture end at the superior apex (Figure 1.6).
6. Create an aortotomy by picking up the aorta wall with forceps and cutting an elliptical patch with scissors (approximately the aortotomy should be a fifth of the circumference of the aorta and three times the renal artery lumen in length).
7. Place a 10/O suture at the superior point of the aortic patch from outside to inside (Figure 1.7) and pass through the aorta to tie outside the vessels at the superior apex of the aortotomy.
8. Create the arterial anastomosis with a running suture starting superiorly (Figure 1.8) anastomosing the donor patch to the recipient aorta, take care not to constrict the anastomosis by tying the suture too tight (Figure 1.9).
9. Remove the inferior vascular clamps first then the superior clamp to reperfuse the kidney (Figure 1.10 and 1.11). Visible peristalsis of the ureter maybe seen if adequate blood supply to the ureter is achieved.

6. Kidney Transplantation – Ureteric Anastomosis

1. Divide any attachments of the bladder from the abdominal wall.
2. Pass a needle (21G) from the left to right of the bladder through both walls.
3. Place straight forcep tips in the needle lumen and pass both back through the bladder such that the forceps are now passing from right to left out of the left side of the bladder.
4. Draw the suture on the donor ureter through the bladder such that the ureter passes in the left bladder defect then out of the right side.
5. Suture the adventitia of the ureter to the adventitia of the bladder with three single interrupted sutures around the entry point with 9/O nylon suture on a round-bodied needle.
6. Cut the ureter proximal to the ligature, thus opening the ureter to allow urine to flow and allow the ureter end to retract into the body of the bladder. Visible production of urine may be observed along with bleeding from peri-ureteric vessels.
7. Close the right side bladder defect with a single interrupted 9/O silk suture.

7. Recovery and Post-operative Care

Replace the gastrointestinal viscera into the abdomen in their original orientation and close the abdominal wall by approximating the rectus muscles with 6/O absorbable suture.

1. Approximate the skin with metal skin clips.
2. Partially reverse the anesthesia with a subcutaneous injection of atipamazole hydrochloride (10 μl/g).
3. Administer analgesia by subcutaneous buprenorphine hydrochloride (0.05 mg/kg) and for fluid support injection 1 ml of subcutaneous 0.9% NaCl.
4. Recover the mouse in a warming cabinet at 28 °C for 24 to 48 hr. Observe the mouse for illness up to the completion of the experiment.
5. Remove metal skin clips 7 – 10 days post operatively.
6. Once the experiment is complete euthanize the mouse by cervical dislocation.
7. Remove and collect the contralateral kidney and allograft for histological analysis.

Results

Renal allograft rejection can be assessed by histological analysis of methacarn-fixed paraffin-embedded tissue sections of the transplanted kidney (Figure 2). Isograft transplantation of kidneys between syngeneic mice results in renal ischemic reperfusion injury, however by 4 weeks the tubules have recovered and are histologically comparable to native kidneys. Acute rejection can be modeled by C57BL/6 kidney transplantation into BALB/c recipients, within 1 week there is diffuse mononuclear cell infiltrat...

Discussion

The most well described manner to perform the arterial anastomosis is to use the distal aorta of the donor, with the renal artery in continuation, in an end-to-side manner to the recipient aorta. We describe the use of an aortic patch, similar to the ‘Carrell patch’ mirroring that performed in human kidney transplantation which we believe to be more convenient. Though reports in the literature of donor and recipient operative time are sparse we believe that utilizing an aortic patch to recipient aorta instead...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Surgical Instruments
Blunt Dissecting Scissors	Fine Science Tools	14072-10	For skin cutting
Curved Castoviejo scissors	Fine Science Tools	15017-10	For tissue cutting
Spring Scissors – straight	Fine Science Tools	15000-08	For suture cutting
Toothed forceps 1x2 teeth	Fine Science Tools	11021-12
2 x Fine Tip forceps (Dumont No.5)	Fine Science Tools	11251-20
Angled Fine Tip forceps (Dumont No. 5/45)	Fine Science Tools	11253-25	For blunt dissecting
Curved Fine Tip forcep (Dumont No.7)	Fine Science Tools	11273-22	Useful to pass around vessels
Curved Crile Haemostat	Fine Science Tools	1300-04
Micro clip applicator with lock	Fine Science Tools	18056-14
2 x Micro serrefines spring width 2mm, jaw length 4mm	Fine Science Tools	18055-04	Microvascular clamps
2 x Colibri 3cm wire retractor	Fine Science Tools	17000-03
Castroviejo needle holder with lock	Fine Science Tools	120660-01
Wound clip applicator	Fine Science Tools	12031-07
7mm wound clips	Fine Science Tools	12032-07	Remove 7 to 10 days after surgery
Equipment
OPMI pico microscope	Carl Zeiss	S100
Thermal cautery unit with fine tip	Geiger	150A
Heat electronic pad	Cozee Cumfort	n/a
Euroklav 23-S	Melag	n/a	Autoclave
Disposable equipment
7/O Silk braided suture	Pearsall	30514
10/O Dafilon (polyamide) suture	B-Braun	G1118099
6/O Vicryl (plygalectin)	Ethicon	W9537
Regular bevel needle, 1 inch, 21G	Bection, Dickinson and Company	305175	For ureteric anastamosis
Regular bevel needle, 5/8 inch, 25G	Bection, Dickinson and Company	305122
Regular bevel needle, 1/2 inch, 30G	Bection, Dickinson and Company	304000
Insulin needle 1ml, 29G	Bection, Dickinson and Company	324827
Insulin needle 0.3ml, 30G	Bection, Dickinson and Company	324826
1 ml syringe slip tip	Bection, Dickinson and Company	300184
5 ml syringe slip tip	Bection, Dickinson and Company	302187
Wypall paper swabs	Kimberley-Clark	L40	sterilised by autoclave
Cotton wool buds	Johnson and Johnson	n/a	sterilised by autoclave
Plain drapes	Guardian	CB03	sterilised by autoclave
Cell culture dish 60mm x 15mm	Corning Incorporated	430166
Dispensing Pin	B-Braun	DP3500L / 413501	Used with NaCl 0.9%
Re-agents and Drugs
(Lacri-Lube) White soft paraffin 57.3%, mineral oil 42.5% and lanolin alcohols 0.2%	Allergan Ltd	21956GB10X
(Videne) Povidone-iodine 10%	Ecolab Ltd	PL 04509/0041
(Vetalar V) Ketamine hydrochloride	Pfizer Animal Health	Vm 42058/4165	100mg/ml solution (dose 200mg/kg)
(Domitor) Medetomidine hydrochloride	Orion Pharma	Vm 06043/4003	1mg/ml (dose 0.5mg/kg)
(Vetergesic) Bupernorphine hydrochloride	Alsto Animal Health	Vm 00063/4002	0.3mg/ml (dose 0.05mg/kg)
(Antisedan) Atipamezole hydrochoride	Orion Pharma	Vm 06043/4004	5mg/ml (dose 2mg/kg)
University of Wisconsin Solution	Belzer Bridge to Life	n/a	dose approximately 500 microlitres/mouse
NaCl 0.9%	Baxter	FKE1323
Heparin Sulphate	non-proprietary	n/a	5000units/ml (dose 5units/mouse)