Advanced Animal Model of Colorectal Metastasis in Liver: Imaging Techniques and Properties of Metastatic Clones

Podsumowanie

The ability of metastatic clones to colonize distant sites depends on their proliferation capacity and/or their ability to survive in the host microenvironment without significant proliferation. Here, we present an animal model that allows quantitative visualization of both types of liver colonization by metastatic clones.

Streszczenie

Patients with a limited number of hepatic metastases and slow rates of progression can be successfully treated with local treatment approaches^1,2. However, little is known about the heterogeneity of liver metastases, and animal models capable of evaluating the development of individual metastatic colonies are needed. Here, we present an advanced model of hepatic metastases that provides the ability to quantitatively visualize the development of individual tumor clones in the liver and estimate their growth kinetics and colonization efficiency. We generated a panel of monoclonal derivatives of HCT116 human colorectal cancer cells stably labeled with luciferase and tdTomato and possessing different growth properties. With a splenic injection followed by a splenectomy, the majority of these clones are able to generate hepatic metastases, but with different frequencies of colonization and varying growth rates. Using the In Vivo Imaging System (IVIS), it is possible to visualize and quantify metastasis development with in vivo luminescent and ex vivo fluorescent imaging. In addition, Diffuse Luminescent Imaging Tomography (DLIT) provides a 3D distribution of liver metastases in vivo. Ex vivo fluorescent imaging of harvested livers provides quantitative measurements of individual hepatic metastatic colonies, allowing for the evaluation of the frequency of liver colonization and the growth kinetics of metastases. Since the model is similar to clinically observed liver metastases, it can serve as a modality for detecting genes associated with liver metastasis and for testing potential ablative or adjuvant treatments for liver metastatic disease.

Wprowadzenie

Patients with liver metastases from primary colorectal cancers (CRC) are characterized by a poor prognosis. The 5-year survival rate for primary nonmetastatic CRC (stages I - III) is estimated as 75 - 88%^3,4, while patients with liver metastases (stage IV) have a 5-year survival rate of only 8 - 12%^5,6. However, metastatic patients represent a heterogeneous group, presenting with different numbers of metastases and different recurrence times. Clinical observations indicate that the number of metastases (which may be proportional to colonizing ability or frequency of colonization) and the size of any single metastasis (proportional to the local growth rate) are independent prognostic factors^1,7. In other words, the success of metastatic clones colonizing the liver depends on two major properties: their ability to grow and their ability to disseminate and survive in the liver microenvironment.

The design of successful clinical models with the capability of capturing and quantifying the properties of metastatic clones can drastically improve our understanding of liver metastasis biology and provide an effective tool for the design of potential therapeutic approaches. Models of experimental liver metastasis have been previously reported^8,9, but neither of them provided the ability to quantitatively capture and describe properties of individual metastatic clones both in vivo and ex vivo.

Here, we present a new, advanced model of liver metastasis that includes the generation of tumor clones with different liver colonization efficiencies and growth properties. We employed a combination of dual-labeling of cancer cells with luciferase and tdTomato fluorescent protein with the generation of monoclonal cell lines that have intrinsic differences in metastatic capacity. In this experimental model, the data indicate that the development of liver metastases can be described in terms of colonization frequency and doubling time (Td), which is consistent with clinical observations. The quantitative nature of this model makes it easily adoptable for drug discovery and diagnostic purposes.

Protokół

All animal procedures were approved by the Institutional Animal Care and Use Committee at the University of Chicago (Protocol # 72213-09) and performed under sterile conditions.

1. Preparations

1. Make 500 mL of medium for the culture of HCT116 tumor cells: Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% Fetal Bovine Serum (FBS), 100 U/mL penicillin, and 100 mg/mL streptomycin.
2. Autoclave the instruments to be used for the spleen injection model, including 3 - 4 surgical towels, gauze, two small Adson pickups, a needle driver, two pairs of scissors, a small clamp, and 3 microclips, at 251 °F for 20 min.
3. Prepare postoperative anesthesia for the mice, to be administered subcutaneously following the spleen injection. Dilute 2 - 4 µg of buprenorphine in 500 µL of 0.9 normal saline per mouse.
4. Prepare aliquots of 150 µg/150 µL of firefly luciferin for intraperitoneal injections during the bioluminescence assays. Store at -20 °C and protect from light.

2. Generation of Luciferase/tdTomato-labeled Monoclonal Cell Lines ^10,11

1. Thaw and maintain HCT116 human colorectal cancer cells and 293FT human embryonic kidney cells in DMEM with 10% FBS, 100 U/mL penicillin, and 100 mg/mL streptomycin. Maintain in culture at 5% CO₂ and 37 °C.
2. Produce a high-titer lentivirus.
   1. On D 1, plate 10 - 12 x 10⁶ 293FT cells between passage 3 and 10 in 15 cm cell culture dishes in 18 mL of complete DMEM (cDMEM) with 10% FBS, 1% penicillin/streptomycin, and 1% nonessential amino acids. Incubate at 37 °C and 5% CO₂.
   2. On D 2, transfect the cells using the following transfection solution:
      1. For each dish, use the following: a DNA mixture of 37.5 µg of pFUG lentiviral vector inserted with the luciferase (Luc2) and tdTomato constructs¹¹ (a gift from Dr. Geoffrey Greene at the University of Chicago), 25 µg of pCMVΔ8.74, and 12.5 µg of pMD2.G resuspended in a total of 1,062 µL of sterile H₂O. Add 188 µL of 2 M CaCl₂.
      2. Add 1,250 µL of 2x Hepes-buffered Saline (HBS, 50 mM Hepes, 1.5 mM Na₂HPO₄, and 180 mM NaCl, pH 7.12) to the DNA/CaCl₂ solution, a drop at a time, while blowing bubbles through the solution with a pipette.
      3. Incubate at RT for 20 min, and then add 15.5 mL of RT cDMEM and chloroquine to make a final concentration of 25 µM.
   3. Aspirate the media in each dish of 293FT cells and replace with the transfection solution. Add 16 mL of the transfection solution slowly, as the plated cells easily dislodge.
   4. On D 3, after 8 - 16 h, remove the transfection solution and wash the cells once with Dulbecco's Phosphate-buffered Saline (DPBS), again taking care not to dislodge the cells. Replace the media with 18 mL of fresh cDMEM with 10 mM Hepes.
      NOTE: Slowly move dishes, aspirate the transfection solution, and add the media through the sidewall of plates so as not to dislodge the cells.
   5. On D 4, at 48 h from the time of transfection, collect the media from the dishes by aspirating slowly with a pipette so as not to dislodge the cells. Centrifuge the collected media at 300 x g for 5 min to precipitate the large cell debris.
   6. Filter the viral supernatant using a 0.45 µm low-protein-binding filter flask and centrifuge using a SW-28 rotor for 2 h at 50,000 x g and 4 °C. Decant the supernatant immediately after the centrifugation finishes and dry the inside of the tube with wipers.
   7. Resuspend the viral pellet in 50 µL of Reduced Serum Medium (RSM) with 1% FBS. Aliquots can be stored at -80 °C for future use (viral stock).
3. Transduce the lentiviruses into the HCT116 cells and generate a panel of tdTomato-positive clones.
   1. Plate the HCT116 cells at a density of 1 x 10⁵ in 24 well plates 1 d before the viral infection.
   2. Dilute 40 µL of resuspended virus (from 2.2.7) in 4 mL of RSM (1:100 dilution) with 1% penicillin/streptomycin and 8 µg/mL polybrene (cRSM).
   3. On the day of infection, wash the cells once with DPBS, and then add 250 µL of diluted virus from step 2.3.2 to each well. Incubate for 4 h at 37 °C and 5% CO₂, and then add 1 mL of cDMEM to each well; incubate at 37 °C and 5% CO₂ for 48 - 72 h.
   4. Resuspend the cells with 1 mL of 0.05% trypsin and 0.53 mM EDTA, and then add 1 mL of cDMEM to neutralize the trypsin. Transfer the cells to a microcentrifuge tube and pellet at 300 x g for 4 min. Wash the pellet 3x in 1 mL of Hanks' Balanced Salt Solution (HBSS) plus 2% FBS.
   5. Resuspend the pellet from step 2.3.4 with FACS buffer (2% FBCS and 2 mM EDTA in PBS) into a single-cell suspension at 1 x 10⁶ cells/mL.
   6. Sort the tdTomato-positive HCT116 cells using a cell sorter, gating for PE-positive cells (excitation/emission: 556/585 nm). Grow the collected cells in a 10-cm dish at 5% CO₂ and 37 °C to generate parental tdTomato-positive HCT116 cells (Figure 1A).
   7. Resuspend the parental tdTomato-positive HCT116 cells from 2.3.6 with 8 mL of 0.05% trypsin and 0.53 mM EDTA for 3 - 5 min, and then add 8 mL of cDMEM to neutralize the trypsin.
      1. Transfer the cells to a 50 mL tube and pellet at 300 x g for 4 min. Remove the supernatant and dilute the parental tdTomato-positive HCT116 cells to 1 cell per 200 µL in cDMEM (Figure 1B).
   8. Plate a single cell (200 µL of the dilution) per well in a 96-well plate at 5% CO₂ and 37 °C (Figure 1C).
   9. Grow individual monoclones in flasks at 5% CO₂ and 37 °C. (Figure 1D).

3. Calibration of Fluorescent Signal Intensity as a Function of Cell Number

1. Plate the transfected HCT116 cells, now referred to as HCT116-L2T, at a density of 0, 10³, 2 x 10⁴, 3 x 10⁵, 5 x 10⁴, 7 x 10⁴, 9 x 10⁴, and 10⁵ cells/well in 96 well plates in triplicates for each density.
2. After 5 h of incubation, quantify the tdTomato fluorescent intensities using IVIS¹⁰.
   1. Click on the image software icon on the desktop to start the software. Click the "Initialize" button to initialize the imaging system. After initialization finishes (which takes about few min), select "Fluorescence", "4 second" exposure time, "Medium" binning, "2" F/stop, "535" excitation filter, and "580" emission filter.
   2. Place the 96 well plate on the imaging station and click on "Acquire" to start imaging. After the image is acquired, click "ROI Tools" in the tool palette and select 12 x 8 from the slit icon.
   3. Create 12 x 8 slits to cover the area of signal on the image of the 96 well plate and click the measurements tab. Observe a window with a table of ROI measurements with units of photons per s per steradian per square cm (photons/s/sr/cm²).
3. Construct a scatterplot with the argument (X axis) equal to the number of cells and the function (Y axis) representing signal intensity. Calculate regression curves using a data analysis software to calculate the amount of cells corresponding to the unit of fluorescent intensity (Figure 2)¹⁰.

4. Animal Model of Liver Metastases

1. Once the HCT116-L2T cells reach 70 - 80% confluency, prepare them approximately 1 h prior to the spleen injection. Dissociate the cells using 0.05% Trypsin in 0.53 mM EDTA for 3 - 5 min, and then neutralize them with an equal amount of cDMEM. Make sure to pipette thoroughly to avoid clumping.
2. Count the cells with an automatic cell counter.
3. Resuspend the cells in 1x DPBS to a concentration of 1.2 - 2 x 10⁶ cells/100 µL. Make sure to pipette and resuspend the cells thoroughly to avoid clumping.
4. Keep the cells on ice until injection, occasionally resuspending them in the tube.
5. Prior to anesthetizing the mice, provide a preoperative anesthetic and fluid bolus by subcutaneously injecting 500 µL of the buprenorphine mixture described in step 1.3. Administer the same dose of additional buprenorphine mixture twice a day until signs of pain(reduced mobility, hunched stature, failure to groom, vocalization when handled) have resolved.
6. Anesthetize 6- to 8-week-old female athymic nude mice with 2% isoflurane in oxygen in an anesthesia chamber. Confirm that the mice are completely under anesthesia by pinching the tail. Use vet ointment on the eyes to prevent dryness while under anesthesia. Transfer each anesthetized mouse to an individual nose cone for the spleen injection. Prior to incision, each mouse should be covered with a sterile surgical drape.
7. Identify the spleen as a purple area seen externally through the skin on the left flank of the nude mice. Using microdissection scissors, make an 8 mm left flank incision on the skin just above the spleen.
   1. Next, lift up on the abdominal wall and make a small incision. Allow air into the abdominal cavity so that the internal organs move away from the incision site. Enlarge the abdominal wall incision to approximately 5 mm.
   2. Expose the spleen by gently applying pressure around the incision with a cotton swab. If needed, the pancreatic fat can be gently manipulated to help with exposure so as not to injure the spleen.
8. Slowly inject 100 µL of cells using a 1 mL syringe with a 27 G needle into the tip of the exposed spleen. Inject slowly, over a period of at least 30 - 60 s, to avoid extra-liver tumors.
9. Place a microclip on the spleen prior to removing the needle at the end of the injection to prevent leakage of the injected cell suspension.
10. Leave the microclip in place for 5 min.
11. 5 min postinjection, perform a splenectomy using a hand-held cautery device for hemostasis. Dissect the splenic hilum, starting from the anterior side. When dissecting large vessels, pre-coagulate the proximal side of the vessels with adjacent fat tissue, using cautery to avoid excessive bleeding.
    NOTE: Methods for hemostasis: coagulate the bleeding point directly with cautery, apply pressure to the bleeding point for 3 - 5 min, or suture-ligate the bleeding point with a 5-0 silk tie.
12. Close the flank incision of each mouse in two layers. First, close the abdominal wall with a 5-0 absorbable braided suture (e.g., vicryl) in a single horizontal stitch. Next, close the skin using a 4-0 nonabsorbable monofilament suture (e.g., prolene), again with a single horizontal stitch.
13. Clean all instruments by spraying 70% isopropanol to maintain sterile conditions between every procedure.
    NOTE: Make sure the animals are warmed while they awake from anesthesia. Monitor all mice post-operatively until they become ambulatory and return to normal activity. Typically, the recovery time is approximately 3 - 5 min. Do not leave animals unattended until they have regained sufficient consciousness to maintain sternal recumbency. Do not return an animal that has undergone surgery to the company of other animals until it has fully recovered.

5. In Vivo Bioluminescent Imaging

1. Perform imaging on a weekly basis to measure and quantify changes in bioluminescence over time.
2. Place mice in an anesthesia chamber and anesthetize them with 2% isoflurane in oxygen. Confirm that the mice are completely under anesthesia by pinching the tails. Use vet ointment on the eyes to prevent dryness while under anesthesia.
3. Next, intraperitoneally inject each mouse with 150 µL of the preprepared firefly luciferin from step 1.4.
4. Place the mice in an IVIS with individual nose cones administering isoflurane. Place the mice in the supine position with spacers in between to minimize the signal to adjacent mice. A maximum of five mice may be imaged at one time.
5. Measure and analyze bioluminescent intensities 3 min after luciferin injection.
   1. After initializing the IVIS as described in step 3.2.1, select "Luminescent", "1 second" exposure time, and "Medium" binning.
   2. Click the "Acquire" button to start imaging. Make sure to perform each imaging at a consistent time (3 min) after the luciferin injection.
   3. After the image is acquired, an image window and tool palette will appear. Click "ROI Tools" and select "1", "2", "3", "4", or "5" from the circle icon, corresponding to the number of mice imaged.
   4. To define Regions of Interest (ROIs), circle the signal area of the luminescent signal in the abdominal cavity of the mouse, and then click "measurements" of the ROI as an arbitrary unit of radiant efficiency ((photons/s/cm²/steradian)/(µW/cm²)). Make sure to have an additional ROI circle of the background.
6. At four weeks post-injection and prior to animal sacrifice, perform Diffuse Luminescent Imaging Tomography (DLIT) using IVIS to evaluate the tumor burden and distribution using real-time 3D reconstruction of bioluminescent intensities of individual tumor colonies.
   1. Anesthetize the mice and inject luciferin, as described in step 5.2.4. DLIT is performed on one mouse at a time.
   2. After initializing the IVIS, as described in step 3.2.1, select "Imaging wizard", "Bioluminescence", and click "Next". Select "DLIT" and click "Next". Select "Firefly" probes and click "Next". Select "mouse" image subject, "Auto" exposure parameter, "C-13 cm" field of view, and "0.5 cm" subject height, and click "Next". Click the "Acquire" button to start imaging.
   3. After the image is acquired, select the "DLIT 3D Reconstruction" tab and the "Analyze" tab and click "Reconstruct" to generate the 3D reconstruction image.
   4. Click "Tools" and "3D Animation". Select "Spin CCW on Y-axis" in the 3D animation window. Click "Record" and "Save" into a .mov format file.

6. Ex Vivo Fluorescent Imaging

1. Sacrifice the mice by cervical dislocation while anesthetized, or according to institutional guidelines at 4 - 6 weeks following the spleen injections.
2. Harvest the liver. Make a horizontal incision from the left to right flank. Grabbing the xiphoid process with a pickup, dissect the falciform, the hepatic vein, and the inferior vena cava.
   1. Dissect the right hepatorenal ligament, the hepatoduodenal ligament, and the left hepatorenal ligament, taking care not to injure the caudate lobe while dissecting the hepatoduodenal ligament. After harvesting the liver, remove the gallbladder, as this will display autofluorescence. Make note of any additional extra-liver tumors present.
3. Take note of the numbers and sizes of liver tumors present macroscopically, and place the harvested livers in DPBS.
   NOTE: Tumors are macroscopically visible to the naked eye as white tumors (for a representative example, see Figure 4).
4. Prior to placement on the imaging sheet, take each liver and gently remove excess liquid by blotting on a paper towel.
5. Measure the fluorescent intensities from each tumor colony using the IVIS.
   1. Select "Fluorescence", "4 seconds" exposure time, "Medium" binning, "2" F/stop, "535" excitation filter, and "580" emission filter. Click the "Acquire" button to start imaging.
   2. After acquiring the image, locate the image window and tool palette. Click "ROI Tools" and select "1" from the circle icon. To define ROIs, circle the signal area of individual tumor colonies on the image, and then click "measurements" of the ROI as an arbitrary unit of radiant efficiency ((photons/s/cm²/steradian)/(µW/cm²)). Make sure to have an additional ROI circle of the background.
6. Calculate the total tumor volume by assuming it to be a sphere. Tumor volume = 4 x π x r³ / 3 (r = radius). Calculate the fraction of tumor colony forming cells (Fc) as the number of tumors in the liver divided by the number of cells splenically injected.
7. Calculate the total cell number per colony (=X) from the linear approximation from step 3.3. Calculate the number of cell divisions (=Y) as Y = log₂X and the Td as Td (day) = 28 / Y.

Wyniki

The goal of this experiment was to establish a consistent and easily reproducible animal model with the potential for the serial quantification of the in vivo metastatic tumor burden and for the estimation of the colonizing frequency and growth kinetics of developing liver metastases. Figures 2-6, with legends, are provided from our previous publication under a Creative Commons CC-BY license¹⁰.

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Dyskusje

The animal model presented in the current report is based on two major approaches. First, in order to ensure the ability to observe metastatic clones with different propensities to colonize and proliferate in the liver, a panel of highly heterogeneous monoclonal cell lines was established, rather than an established unfractionated cancer cell line^12,13. The monoclonal approach to metastasis development is justified by recent genomic data¹⁴ and was successfully used previously to model the metastatic...

Materiały

Name	Company	Catalog Number	Comments
IVIS Spectrum In Vivo Imaging System	Caliper Life Sciences	124262	In Vivo imaging system
LivingImage 4.0 Software	Caliper Life Sciences	128165	Imaging software
VAD-MGX Research Anesthetic Machine	Vetamac	VAD-MGX	Inhalation anesthesia machine
DMEM	Gibco	11965-118	Cell culture reagents
DPBS	Gibco	14190250	Cell culture reagents
Penicillin/Streptomycin, liquid (10,000 units penicillin;10,000 μg streptomycin)	Invitrogen	15140163	Cell culture reagents
HBSS	ThermoFisher	24020117	Cell culture reagents
Buprenex Injection (0.3 mg/mL)	Reckitt Benckiser Healthcare Ltd.	12496-0757-5	Buprenorphine hydrochloride
Gemini Cautery System	Braintree Scientific	GEM 5917	Hand-held cautery for splenectomy
Micro Clip; Straight; 70 Grams Pressure; 1.5 mm Clip Width; 10 mm Jaw Length	Roboz Surgical Instrument	RS-5426	Hemoclip: Hemostasis instruments after spleen injection
D-luciferin, potassium salt	Goldbio Technology	LUCK-1G	Luciferin potassium salt
Opti-MEM I Reduced Serum Medium	Gibco	31985062	Reduced Serum Medium
TC20 Automated Cell Counter	BIO-RAD	1450102	Automatic cell counter
JMP10 software	SAS Institute		Data analysis software
BD FACSAria II cell sorter	BD Biocsiences		Cell sorter