An In Vivo Murine Sciatic Nerve Model of Perineural Invasion

Podsumowanie

We describe an in vivo murine model of perineural invasion by injecting syngeneic pancreatic cancer cells into the sciatic nerve. The model allows for quantification of the extent of nerve invasion, and supports investigation of the cellular and molecular mechanisms of perineural invasion.

Streszczenie

Cancer cells invade nerves through a process termed perineural invasion (PNI), in which cancer cells proliferate and migrate in the nerve microenvironment. This type of invasion is exhibited by a variety of cancer types, and very frequently is found in pancreatic cancer. The microscopic size of nerve fibers within mouse pancreas renders the study of PNI difficult in orthotopic murine models. Here, we describe a heterotopic in vivo model of PNI, where we inject syngeneic pancreatic cancer cell line Panc02-H7 into the murine sciatic nerve. In this model, sciatic nerves of anesthetized mice are exposed and injected with cancer cells. The cancer cells invade in the nerves proximally toward the spinal cord from the point of injection. The invaded sciatic nerves are then extracted and processed with OCT for frozen sectioning. H&E and immunofluorescence staining of these sections allow quantification of both the degree of invasion and changes in protein expression. This model can be applied to a variety of studies on PNI given its versatility. Using mice with different genetic modifications and/or different types of cancer cells allows for investigation of the cellular and molecular mechanisms of PNI and for different cancer types. Furthermore, the effects of therapeutic agents on nerve invasion can be studied by applying treatment to these mice.

Wprowadzenie

Nerves form a specific tumor microenvironment that stimulates cancer growth and migration^1,2,3. Perineural invasion (PNI) is the process through which cancer cells invade in and around the nerves. It may be considered as a unique route of metastasis since cancer invasion extends away from the sites of origin along nerves. PNI is found in several cancer types including pancreatic, prostate, head & neck, salivary, cervical, and colorectal cancers with an incidence ranging from 22% to 100%^1,2. PNI is associated with pain and correlates with poor prognosis and worse survival rates^1,2.

Developing models of perineural invasion is essential to elucidate the cellular and molecular mechanisms of this process, and to test candidate therapeutic agents to decrease PNI. In vitro methods of studying interactions between cancers and nerves include the co-culture of cancer cells with nerve explants⁴, with dorsal root ganglions^5,6,7, or with specific cells from the nerve microenvironment such as Schwann cells⁷. In vivo approaches, however, are more physiologically relevant, include the use of cancer mouse models in which cancer has been induced or transplanted and have the advantage of accounting for the entire nerve microenvironment. In orthotopic models of pancreatic or prostate cancer, PNI has been reported^8,9,10 and the incidence of PNI may be recorded, but because of the small size of the nerves in those organs, it is difficult to see the entire nerve and therefore to quantify the extent of PNI. The model we describe here is an in vivo model of PNI in which cancer cells are injected into the sciatic nerve of mice through a simple surgical procedure¹¹. The heterotopic transplant invades within the nerve toward the spinal cord. The length of the nerve invasion from the site of injection to the spinal cord may be measured, as well as the volume of the cancer within the nerve. Importantly, the invaded nerve can also be collected for a variety of assays including microscopic, and molecular analyses. A variety of cancer cells can be tested, and the host mice that have been genetically modified or treated with specific compounds may be used as well. This powerful assay allows for the cancer cells and the host microenvironment to be modified for investigation into the mechanisms of PNI.

Protokół

All of the procedures with animal subjects were approved by the Institutional Animal Care and Use Committee at Memorial Sloan Kettering Cancer Center.

1. Preparation of the Cancer Cells

1. Harvest sub-confluent Panc02-H7 cells with 0.25% trypsin for 5 min at 37 °C. Collect the cells in a 15 mL centrifuge tube.
   NOTE: The cells are grown in T-225 flask, which contains about 12 x 10⁶ cells per flask at 80% confluency and 4 mL trypsin/ flask is used.
2. Centrifuge the cells at x 900 g at 4°C for 5 min. Wash the cells by resuspending the cell pellet in 1 mL of PBS (by pipetting up and down twice), and transfer the suspension to a 1.5 mL microcentrifuge tube on ice.
3. Centrifuge the cells again at x 900 g at 4°C for 5 min, and discard the supernatant without disturbing the pellet. Keep the pelleted cells on ice until injection.

2. Preparation of the Mice and Surgery

Note: 8-week-old, male and female C57BL/6J mice are used in this study. The surgery conditions follows the IACUC rules of our institution. The instruments are sterilized, the surgical working surface is disinfected, the animal is disinfected and the surgeon wears sterile gloves.

1. On the day before the surgery, anesthetize the mouse using 2% isoflurane and then remove the fur along the length of femur on the dorsal side with either a thin razor or a chemical hair removal agent.
2. On the day of the surgery, anesthetize the mice using 2% isofluorane in an induction chamber. Confirm the anesthetization by a toe pinch stimulus and a lack of response.
3. Apply vet ointment on eyes to prevent dryness under anesthesia.
4. Place the anesthetized mouse on its ventral side, and gently secure each limb with hypoallergenic tape to create mild tension in the limb to be injected. Anesthesia is maintained using isoflurane delivered via a precision vaporizer and nose cone.
5. Clean the injection site with Betadine, then again with 70% alcohol. Repeat this process two more times. Make sure that no loose hair remains on the surgical field.
6. Make a 1 cm incision with small scissors about 2 mm below and parallel to the femur. Retract the skin with forceps laterally to expose the muscles underneath.
7. The sciatic nerve runs deep to the gluteus maximus and biceps femoris muscles. Separate these two muscles along a fascial plane with small scissors and expose the sciatic nerve underneath. Free the nerve from the surrounding muscles using blunt dissection.
8. Draw 3 μL of cancer cells (about 50,000 cells) from the pellet into a 10 μL syringe.
   NOTE: Alternatively, draw 3 μL of PBS as a control.
9. Place a small metal spatula underneath the nerve at the point of injection for support. Under visualization with a dissecting microscope, insert the needle into the nerve against the metal base, keeping the needle as parallel to the nerve as possible upon insertion. Be careful as not to puncture through the back of the nerve. Minimize the handling of nerve as much as possible throughout this process.
10. Slowly inject into the nerve over 5 s. A formation of a bulb in the injection area indicates a good injection. Then leave the needle in place for 3 s before removing the needle gently. Keeping the needle in place for 3 s minimizes backflow of the cells out of the nerve.
    NOTE: Injection can be performed toward the distal nerve or the spinal cord. It is important to remain consistent within a set of experiments. If the cells spill outside, the animal should not be included in the analysis of the experiment. With experience, these events are very rare.
11. Return the nerve to its original position. Cover the nerve with the overlying muscles. Treat the mice with proper analgesia, and then close the skin with 5-0 Nylon sutures.
12. Place the mouse alone in a clean cage for observation during recovery, until it fully awakens from anesthesia.
    NOTE: It takes 5-15 min for the animal to regain full consciousness. The animal is not left unattended until it has regained sufficient consciousness to maintain sternal recumbency. The animal is not returned to the company of other animals until fully recovered. Thereafter, evaluate recovery at least once every 24 h for 72 h.

3. Sciatic Nerve Extraction

1. On postop day #7, euthanize the mice with CO₂. Place the mouse on its ventral side, and stabilize the distal limbs using pins.
2. Remove the skin on the dorsal side of the injected limb and torso.
3. Using blunt dissection, expose the sciatic nerve deep to the muscles.
4. The nerve courses between the ilium and the sacrum. To have access to the nerve at the spinal cord region, separate the two bones. First insert closed scissors in the narrow area where the sciatic nerve is located and then open the scissors while holding the mouse. Be delicate and maintain the integrity of the sciatic nerve during the dissection.
5. Carefully dissect the sciatic nerve distally to the end of the femur, and proximally to the spinal cord.
6. NOTE: Invaded nerves are extremely fragile and prone to breaking under tension or forceful handling.
7. Harvest the nerve by first cutting its distal end. Carefully lift the nerve while freeing it from adjacent tissue. Cut the nerve at the proximal end, as close as possible to its exit from the spinal column.
8. Record then gross length of invasion using a Vernier caliper. This macroscopic estimation is only indicative.

4. Nerve Processing and Quantification

1. Embed the dissected nerve in OCT compound. Make sure to place nerves longitudinally and as flat on the bottom of the mold as possible.
2. Indicate on the cassette the proximal and distal side of the nerve by marking the letter P and D.
3. Place embedded nerves on top of dry ice, if they are not sectioned immediately. Sample could be preserved at -80 °C for several weeks.
4. Section samples using a Cryostat microtome at 5 μm thickness and place sections on glass slides. If possible, fit 2 nerve sections per slide. Indicate proximal side of the nerve.
5. Stain slides using H&E staining¹².
6. Digitally scan stained nerve sections with a slide-scanner that provides high-resolution digital data.
7. Using imaging software, quantify the length of invasion by clicking the measure distance button, area of invasion, or other desired parameters. For a good estimation of the length of invasion, use multiple sections (2 to 4) of the same nerve.

Wyniki

This method describes the surgical implantation of pancreatic cancer cells into the murine sciatic nerve to create an in vivo model of quantifiable nerve invasion. Figure 1 illustrates the anatomical location of the sciatic nerve and the site of injection. Figure 2 shows the two sciatic nerves of a nude mouse. A PBS injected nerve (left) may be compared to a nerve injected with MiaPaCa-2 cancer cells (right). The ne...

Dyskusje

In this protocol we describe an in vivo murine model of perineural invasion that allows for the quantification of sciatic nerve invasion by pancreatic cancer cells. This model enables the study of molecular mechanisms of nerve invasion. Successful experiments using this technique require a careful approach to three critical steps in the process: 1) the injection of cancer cells (steps 2.7, 2.8), 2) the extraction of invaded nerves (step 3.4), and 3) processing of harvested nerves (step 4.1).

Materiały

Name	Company	Catalog Number	Comments
Mouse			Number and age variable depending on experimental needs
Cell culture media (PBS, Trypsin, and DMEM+10% FBS)	Any		Steps 1.1, 1.2, 1.3.
Conical centrifuge tube, 50 mL	Falcon	352098	Step 1.1
Microcentrifuge tube 1.5 mL	Axygen	MCT-150-C-S	Step 1.2
Electric razor	WAHL	9962	Step 2.1. Can be substituted with commercial hair removal agent
Isoflurane, 250 mL	Baxter	1001936060	Step 2.2
Hypoallergenic surgical tape	3M Blenderm	70200419342	Step 2.3
Betadine Swapsticks	PDI	SKU 41350	Step 2.4
Webcol Alcohol Preps	Covidien	5110	Step 2.4
Sterile surgical tools (scissors and forceps)			Steps 2.4, 2.5, 3.3, 3.4, 3.5
10 μL Hamilton syringe	Hamilton	80308	Steps 2.7, 2.8
Steel Micro spatula	Fisher Scientific	S50823	Step 2.7
Dissecting microscope			Step 2.7
Bupivacine, 1 g	Enzo Life Sciences	BML-NA139-0001	Step 2.9. Reconstitute to 0.5%
5-0 Nylon suture	Ethicon	698H	Step 2.9
Tissue-Tek O.C.T. Compound	VWR	25608-930	Step 4.1
Tissue-Tek Cryomold Molds	VWR	25608-916	Step 4.1