Murine Model of Metastatic Liver Tumors in the Setting of Ischemia Reperfusion Injury

Podsumowanie

We describe in detail a clinically relevant colorectal cancer liver metastases (CRLM) tumor model and the influence of liver ischemia reperfusion (I/R) in tumor growth and metastasis. This model can help to better understand the mechanisms underlying surgery-induced promotion of liver metastatic growth.

Streszczenie

Liver ischemia and reperfusion (I/R) injury, a common clinical challenge, remains an inevitable pathophysiological process that has been shown to induce multiple tissue and organ damage. Despite recent advances and therapeutic approaches, the overall morbidity has remained unsatisfactory especially in patients with underlying parenchymal abnormalities. In the context of aggressive cancer growth and metastasis, surgical I/R is suspected to be the promoter regulating tumor recurrence. This article aims to describe a clinically relevant murine model of liver I/R and colorectal liver metastasis. In doing so, we aim to assist other investigators in establishing and perfecting this model for their routine research practice to better understand the effects of liver I/R on promoting liver metastases.

Wprowadzenie

The liver is one of the most common sites for the development of metastatic disease¹. Mortality is almost invariably attributable to complications associated with tumor growth in the liver. In patients with metastatic solid tumors in the liver, surgery remains a crucial intervention for disease control and a possible curative approach. However, the vast majority of patients ultimately present with recurrent disease, predominantly in the liver^2,3. During hepatic surgery, intraoperative bleeding is common, often necessitating blood transfusion and different technical approaches for control of bleeding, including vascular clamping methods. However, such measures cause hepatic ischemia/reperfusion (I/R) to the liver tissue. The adverse effects of I/R on hepatocellular function have been well documented. The liver I/R insult ignites inflammatory cascades during the restoration of blood flow via inflammatory pathways⁴. Not only does liver I/R injury contribute to liver failure, but current evidence also shows that I/R injury stimulates tumor cell adhesion, and promotes the incidence of metastases formation and the growth of existing micrometastatic disease⁵. We have previously reported that surgical stress induces activation of immune cells which not only helps in the growth of the primary tumor, but also facilitates metastases by capturing cancer cells within the circulation⁶.

Here we describe in detail a technique to establish a liver metastasis mouse tumor model. In this model, we also present a method to induce hepatic ischemia reperfusion injury which acts as a surrogate to the surgical stress present clinically during hepatectomies. The combined methods of cancer injection and hepatic I/R can successfully interpret the development of CRLM in patients who have undergone primary tumor resection.

Protokół

All animal protocols are approved by the Institutional Animal Care and Use Committee and adhered to the National Institutes of Health (NIH) Guidelines. Instruments used for any surgical procedure were thoroughly sterilized.

1. Initial preparation

1. Before injecting cancer cells into the mouse spleen, autoclave and sterilize all instruments to be used during the procedure.
2. Sterilize and/or autoclave a heating pad, surgical gloves, gauze, pairs of scissors, small clamps, vessel dilator, surgical forceps, and a needle holder.
3. Prepare post-operative analgesic (0.1 mg/kg of buprenorphine) to be administered after splenectomy and every 12 h for 2 days.

2. Cell culture

1. Ensure that cancer cells are free from mycoplasma contamination by using a mycoplasma ELISA kit.
2. Prepare a 500 mL solution of Dulbecco's Modified Eagle medium (DMEM) culturing medium at 4 °C for the culture of murine colorectal cancer cells (MC38). The culturing media should be supplemented with 10% heat-inactivated fetal bovine serum (FBS), 100 U/mL of penicillin, 100 µg/mL of streptomycin, 15 mM of HEPES and 200 mM of L-glutamine.
3. Culture cancer cells in a DNAse- and RNAse-free flask (75 cm²). Incubate the cell culture in a cell/tissue humidified incubator containing 5% CO₂. Maintain temperature at 37 °C.
4. Once the proliferating cells reach 90–100% confluency, aspirate the old media, wash cells with 1x phosphate-buffered saline (PBS) and then treat them with 1x trypsin (0.25%) to detach cells from the flask.
5. Collect cells in a 15 mL conical tube and centrifuge for 5 min at 700 x g.
6. Aspirate the media and wash with 1x PBS twice by repeated centrifugation.
7. Proceed to confirm cell viability by staining cells with trypan blue stain (0.4%).
8. Resuspend cells to a concentration of 1 x 10⁶ cells/ 100 µL in 1x PBS. Pipet cells thoroughly to avoid any clumps. Keep cancer cells on ice prior to injection.

3. Injecting tumor cells

1. Anesthetize 8–12-week-old male (C57BL6) mice by administering ketamine (150 mg/kg) and xylazine (12 mg/kg) intraperitoneally using a 1 mL 25 G (0.5 mm x 16 mm) needle.
2. Shave the abdominal skin of the mice using clippers to avoid any postoperative infections.
3. Place mice on the magnetic fixator retraction system. Confirm that the mice are completely under the effect of anesthesia by pinching a toe or the tail.
4. Add saline drops into the eyes to avoid dryness during the procedure.
5. Scrub povidone-iodine solution (7.5%) to the shaved abdominal wall to disinfect the skin before making a surgical incision.
6. Initially lift the skin with the toothed forceps and make a midline incision with the help of surgical scissors. Then, lift the abdominal muscle and peritoneum to create a midline incision of approximately 3 cm length (midabdominal to xiphoid process to expose the abdominal contents. Take caution not to extend the incision beyond the xiphoid process to avoid extensive bleeding.
7. Place the hemostat at both sides of the incision and under the xiphoid process. Extend the abdomen by pulling the tail downward and taping it. Use the 6-inch sterile cotton tip applicator to separate and expose the spleen from the pancreatic fat tissue.
8. Before injection into the spleen, vortex the cancer cells to avoid any cell clumps.
9. Use a 0.5 mL 28 G (0.36 mm x 13 mm) insulin syringe for injection. Avoid air bubbles.
10. Slowly and carefully inject 100 µL of cells into the tip of the spleen. Place a cotton tip and add gentle pressure to avoid backflow into the abdominal region. A successful injection can be observed by identifying the change in the color of the liver during the injection.
11. Moisten a sterile gauze with 1x PBS and place it over the dissected area.
12. Transfer the mice onto a heating pad for 15 mins to allow cancer cells to circulate within the system.
13. To proceed with surgical ischemia and reperfusion injury, follow steps 5.3-5.10. 
    NOTE: This procedure is to study the effect of I/R induced establishment of metastatic foci.

4. Splenectomy

1. To perform a splenectomy, use a hand-held cautery device. Carefully lift the spleen with smooth forceps and cauterize the splenic blood vessels to avoid excessive bleeding. Remove spleen by transecting the vessels at the cauterized section.
2. Immediately following the procedure, close the incision in a double layer pattern by first suturing the muscle layer and then the skin. Use 4-0 polypropylene sutures for both the abdominal wall and the skin.
3. Before repeating the procedure on another animal, disinfect all instruments by either spraying them with 70% isopropanol or inserting them into a bead bath.
4. Place mice back into original cages and look for signs of distress and post-surgical pain.
5. Inject post-operative analgesic (Buprenorphine 0.1 mg/kg) every 12 h for 2 days to avoid post-surgical pain.

5. Ischemia reperfusion Injury

1. At 5 days after the first laparotomy, anesthetize mice by administering ketamine (150 mg/kg) and xylazine (12 mg/kg) intraperitoneally using a 1 mL 25 G (0.5 mm x 16 mm) needle. Follow steps 3.3–3.4.
2. Scrub povidone-iodine solution (7.5%) on the shaved abdomen of the mouse to disinfect the skin and perform a midline laparotomy as described above in step 3.6.
3. Using two moistened cotton tips, gently move the intestine from the cavity to expose the associated structures, including the portal vein. Dissect the liver hilum free of the surrounding tissue.
4. Lift up the median and left lateral lobes against the diaphragm. Separate the quadrate lobe from the left lateral lobe by dissecting the liver hilum with the spring scissors using an operating microscope to allow clear visibility towards the portal triad structure.
5. Place a small moist cotton swab between the median lobe and right lateral lobe to create sufficient space for clamping. Using the vessel dilator forceps, carefully pass the 10 cm thread (4.0 polypropylene suture) to lift the portal triad. Occlude all structures in the portal triad (hepatic artery, portal vein, and bile duct) to the left and median liver lobes by placing a microvascular clamp using a micro-serrefine clamp applicator with lock.
6. If the lobes do not show significant blanching, readjust the clamp by removing and reapplying.
   NOTE: If the immediate blanching of the liver does not occur even after readjusting the clamp, carefully consider whether or not to proceed with the I/R.
7. Remove the small cotton swab placed between the median and right lateral lobes. Gently replace the intestine into the abdominal cavity. Cover the abdominal wall with a moist gauze (soaked with 1x PBS) and cover with a plastic wrap to minimize evaporative loss.
8. Place the mouse on the heating pad and apply the clamp for a period of 60 min.
9. Throughout the ischemic interval, seek evidence of ischemia injury by visualizing the pale blanching of the right medial and left medial and lateral lobes.
10. Initiate reperfusion by removing the clamps after the 60 min period.
    NOTE: Evidence of reperfusion can be observed by an immediate color change of the median and left lateral lobes.
11. Immediately following reperfusion, close the incision with a double layer suture pattern by first suturing the muscle layer and then the skin. Use the 4-0 polypropylene suture with the help of a needle holder to close the abdominal wall and the skin.
12. Before repeating the procedure on another animal, disinfect all instruments by either spraying them with 70% isopropanol or inserting them into a heated bead bath.
13. Place mice back into original cages and look for signs of distress and post-surgical pain.
14. Inject post-operative analgesic (0.1 mg/kg of buprenorphine) every 12 h for 2 days to avoid post-surgical pain.
15. For liver I/R sham mice, perform laparotomy, hilum dissection and abdominal sutures.
    NOTE: The role of surgical stress influencing the establishment of liver metastases can be investigated through two different experimental designs. The above protocol (Model-1) is used to establish micrometastatic liver disease and study the effect of liver I/R on their growth (Figure 1A). Alternatively, liver I/R and tumor injection can be performed concurrently (Model-2) to study the effect of I/R injury in the establishment of new metastatic foci (Figure 1B). To do this, inject cancer cells into the spleen as described above and allow them to circulate for 15 min. Perform liver I/R or sham surgery after the circulating period for 60 min. Perform lateral splenectomy 60 min later, and then close the laparotomy incision.

6. Assessment of operated mice

1. During the surgical procedure ensure that the mice are under the influence of stage III anesthesia by performing palpebral and corneal reflex test. Additional anesthetic dose must be given upon the signs of reflexes.
2. Provide post-operative analgesic (Buprenorphine 0.1mg/kg) right after the surgery and every 12h for 2 days to avoid post surgical pain.
3. Allow mice 30–60 min of recovery time from anesthesia. Constantly monitor mice and do not leave them unattended until complete recovery.
4. Look for distress signs such as hunched back, closed eyes, slow movement, and failure to groom. Treat accordingly until mice return to their normal activity.
5. Supplimental care including fluids, heat, Yohimbine reversal agent for xylazine, soft paper towel bedding (to avoid aspiration) should be provided after the surgery to improve the recovery period.

7. Assessment of liver ischemia reperfusion injury

1. Immediately after applying the clamp, make sure the pale blanching of the median and left lateral lobes occurs compared to the caudate and quadrate lobes.
2. Assess liver ischemia injury by measuring serum alanine transaminase (sALT), serum aspartate transaminase (sAST) and serum lactate dehydrogenase (sLDH) levels. The blood can be drawn from the facial vein to extract serum 3–6 h after the initiation of reperfusion. Perform liver histology to analyze the percent tumor area within the ischemic lobe.

Wyniki

All wildtype (C57BL6) mice (n = 20) were subjected to the liver metastases model using the protocol described above. All injected mice with or without ischemia reperfusion injury survived until the date of sacrifice. The schematic diagram Figure 1A of a cancer-injected liver illustrates the clamping of the portal triad (hepatic artery, portal vein, and bile duct) which induces a partial liver ischemic (70%) insult towards the median and left lateral lobes. An increase in the number of liver ...

Dyskusje

The animal model described in this manuscript is based upon two major approaches. The first is to recognize the ability of cancer cells to localize and proliferate in the liver lobes. The second is to study the effect of hepatic ischemia reperfusion injury influencing the tumor growth and metastases. This model permits the relevant study of liver metastases in the absence of secondary metastases in an immunocompetent mouse. The model is useful in addressing the questions of metastatic efficiency, such as cell survival ex...

Materiały

Name	Company	Catalog Number	Comments
Dulbecco's Modified Eagle Medium	Lonza	12-614F
Fetal Bovine Serum	Lonza	900-108
L-Glutamin	Gibco	25030-081
Penicilin	Fisher scientific	15-140-122
Stretomysin	Fisher scientific	15-140-122
HEPES	Fisher Scientific	SH3023701
Trypsin	Hyclone	sh30042.02
Cell culture Flask 75cm	5 Cells Star	658170
15ml PP Conical Tubes	BioExcell	41021037
Trypan Blue Stain	Giibco	15250-061
Gauze	Fisherbrand	1376152
Cautry	Bovie	AA01
Microvascular clamp	Finescience tools	18055-03
Micro-Serrefine clamp applicator with lock	Fine science toosl	FST-18056-14
Spring scissor	Fine science toosl	FST-15021-15
Vessel Dilator	Fine science toosl	FST-00276-13
Magnetic fixator Retraction system	Fine science toosl	FST-18200020
Micro-Adson Forceps	Fine science toosl	FST-11019-12
Micro-Adson Forceps	Fine science toosl	FST-11018-12
4-0 polypropylene suture	Ethicon	K881H
Needle holder	Harvard Apparatus	72-8826
Heating Pad	Fisher scientific	1443915
Clipper	Oster	559A
Povidone-Iodine solution	Medline	MDS093945
Syringe 1ml 25G	BD safety Glide	305903
Insulin syringe 0.5 ml	BD insulin Syringes	32946
Cotton -Tipped Applicator	Fisher Scientific	23-400-101
Surgical Microscope	Leica	LR92240
Mycoplasma Elisa Kit	Roche	11663925910
Ketamine	Putney	#056344
Xylazine	NADA	#139-236
ALT strip	Heska	15809554
AST strip	Heska	15809542
LDH strip	Heska	15809607