Ultrasound Imaging-guided Intracardiac Injection to Develop a Mouse Model of Breast Cancer Brain Metastases Followed by Longitudinal MRI

Summary

A breast cancer brain metastasis mouse model is established with ultrasound imaging-guided intracardiac injection of MDA-MB231/Br-GFP cells. Development of multifocal intracranial metastases has been monitored longitudinally using high-resolution 9.4 T MRI.

Abstract

Breast cancer brain metastasis, occurring in 30% of breast cancer patients at stage IV, is associated with high mortality. The median survival is only 6 months. It is critical to have suitable animal models to mimic the hemodynamic spread of the metastatic cells in the clinical scenario. Here, we are introducing the use of small animal ultrasound imaging to guide an accurate injection of brain tropical breast cancer cells into the left ventricle of athymic nude mice. Longitudinal MRI is used to assessing intracranial initiation and growth of brain metastases. Ultrasound-guided intracardiac injection ensures not only an accurate injection and hereby a higher successful rate but also significantly decreased mortality rate, as compared to our previous manual procedure. In vivo high resolution MRI allows the visualization of hyperintense multifocal lesions, as small as 310 µm in diameter on T₂-weighted images at 3 weeks post injection. Follow-up MRI reveals intracranial tumor growth and increased number of metastases that distribute throughout the whole brain.

Introduction

Brain metastasis is the most common intracranial malignancy in adults. The prognosis is extremely poor, with a median survival of 4-6 months even with aggressive treatment. Breast cancer is one of the three major primary cancers with a high morbidity of brain metastasis^1-3. Several brain-tropic breast cancer lines are capable of developing brain metastases after intracardiac or intracarotid injection⁴. Direct injection of tumor cells into the left ventricle can bypass the lung capillary bed and thus increase the incidence of forming brain metastases while minimizing visceral metastases. The MDA-MB231Br line is one of the most widely used human breast cancer lines to develop brain metastasis in rodent models^5,6.

Like many other studies^4,7, we have performed a manual procedure of intracardiac injection in our previous studies. However, only 50% successful rate was obtained with the manual injection and a fraction of mice died from the repeated invasive procedures if prior trials failed. Here, we are introducing the use of an imaging-guided procedure to secure the injection of brain-seeking breast cancer cells into the left ventricle of athymic mice. Longitudinal high resolution MRI is applied to follow intracranial development of brain metastases.

Protocol

All animal procedures were approved by the Institutional Animal Care and Use Committee of University of Texas Southwestern Medical Center.

1. Preparation of the MDA-MB231/Br-GFP Cells

1. Retrieve and culture the MDA-MB231/Br-GFP cells (kindly provided by Drs. Palmieri and Steeg, NCI) in DMEM medium containing 10% FBS, 1% glutamine and 1% penicillin/streptomycin.
2. Observe the condition of the cells and color of medium, and replace medium every 2-3 days.
3. Trypsinize and collect the cells when 80% confluence is reached as outlined in steps 1.3.1-1.3.5:
   1. Remove the old medium completely and add 5 ml PBS (1x) to wash the cells gently. Remove the PBS from the dish.
   2. Add 1.5 ml Trypsin in the dish; tilt the dish gently to ensure all the cells are covered by Trypsin. Put the dish back to the cell incubator and keep it at 37 °C for 1 min.
   3. Take the dish out of incubator and observe the cells under optical microscope to ensure the cells detach from the dish.
   4. Add 3 ml medium to stop the effect of trypsin. Collect the cell mixture in a centrifuge tube. Centrifuge the mixture at 2,000 rpm for 5 min.
   5. Remove the medium carefully and resuspend the cells in 5 ml serum free medium until homogenous.
4. Count appropriate number of cells and resuspend them in serum free DMEM medium with a final concentration of 1.75 x 10⁵ cells in 100 µl volume.
   1. Take 50 µl cell mixture and add 50 µl Trypan Blue. After mixing, take 10 µl mixture and carefully add to the cell counting slide. Use multiple samples to ensure accurate cell number estimation.
   2. Stick in the cell counting slide, one end at a time and the cell counter starts counting automatically. Take average of all the counting results and calculate the total cell number.
   3. Centrifuge the cells again and resuspend them in the appropriate volume of serum free medium to result in the final concentration of 1.75 x 10⁵ cells/100 µl volume.
5. Place cells on ice prior to intracardiac injection.

2. Ultrasound Imaging-guided Intracardiac Injection

1. Use female nude mice (BALB/c nu/nu) between 6-8 weeks old.
2. Log in the imaging system. Initialize the transducer 704 (40 MHz).
3. Start a new study and fill in the information.
4. Anesthetize (3% isoflurane/100% O₂ in an induction chamber) and maintain the animals with isoflurane (2%) in 100% O₂ (1 dm³/min) during the whole procedure via a nose cone. Anesthesia is confirmed when no withdrawal reflex is observed with toe pinch.
5. Set the temperature of the imaging table to 37 °C. Tape the anesthetized mouse to the heated imaging table in supine position.
6. Keep the ultrasound gel at 37 °C prior to imaging. Apply the gel to the chest of the mouse.
7. Mount the transducer in the holder. Lower the transducer till the desired imaging depth is reached. Move the stage until the left ventricle is identified with the ascending aorta as the landmark (Figure 1A). Lock the stage when a clear view of left ventricle is visualized.
8. Draw 100 µl of cell mixture into a 1 ml syringe with a 22 G needle. Place and fix the syringe on the syringe mount.
9. Move the syringe forward towards the mouse chest and carefully move it side to side until the needle tip is in the imaging field of view (before entering the mouse).
10. Adjust the needle height and angle to aim down the left ventricle.
11. Penetrate the syringe needle into intercoastal space  promptly through skin and muscle layers into the left ventricle under the guidance of ultrasound imaging.
    An indication of successful insertion of the needle into the left ventricle is the reflux of fresh arterial blood (pink color in contrast to dark red venous blood) into the syringe
12. Inject the cell mixture slowly (Figure 1B).
13. Upon completion, withdraw the needle, lift up the transducer, clean the ultrasound gel with dampened gauze and remove tape.
14. Prepare a clean cage with a preheated pad.
15. Place the animal on the pad and observe the animal till full recovery.
16. Monitor the behavior of the animal every 24 hr for two days.
17. General conditions and neurologic signs of complications in experimental mice are routinely monitored.

3. MRI Monitoring of Intracranial Tumor Development

1. Use a 9.4 Tesla magnet to monitor intracranial development of brain metastases.
2. Initiate MRI two weeks after tumor implantation and repeat once a week for up to three weeks.
3. Sedate the animals with 3% isoflurane and maintain them under general anesthesia (1.5% isoflurane).
4. Monitor and maintain the animal body temperature and respiration constant throughout the experiment.
5. High resolution multislice (14 slices with 1 mm thick, no gap) T₁- and T₂-weighted coronal images, covering the region from the frontal lobe to the posterior fossa, are acquired with the following parameters: T₁-weighted images: spin echo multiple slice (SEMS), TR/TE = 400 msec/20 msec, matrix: 256 x 256, FOV 20 x 20 mm, in plane resolution: 78 x 78 µm². T₂-weighted images: fast spin echo multiple slice (FSEMS) sequences, TR/TE = 2500 msec/48 msec, 8 echo trains, matrix: 256 x 256, FOV 20 x 20 mm, in plane resolution: 78 x 78 µm ^28,9.
   Tumor lesions appear brighter than normal brain tissues on T₂-weighted images.
6. Tumor size is determined on T₂-weighted images by manually outlining the enhancing portion of the mass on each image by using MATLAB programs written by us⁸.
   Given most of the tumor diameters are smaller than the slice thickness (1 mm), the tumor size is presented as in plane area rather than the volume.

4. H&E Staining Confirming the Metastases

1. Sacrifice the mice immediately after the last MR scan, dissect the tumor-bearing brains and embed it in O.C.T medium and frozen in -80 °C.
2. Section a series of 10 µm-thick coronal brain specimens with cryostat.
3. Perform H&E staining on the brain sections.

Results

With the high spatial resolution of MRI (78 µm in plane resolution), hyperintense lesions can be identified as small as 310 µm in diameter (Figure 2). Since the metastases in this study are very small and development of necrosis and edema is minimal, the hyperintense lesion on T₂-weighted images truly represented the tumor mass.

Longitudinal MRI studies allow in vivo noninvasive evaluation of tumor growth. As shown in Figure 3

Discussion

In the present study, we have demonstrated that ultrasound imaging-guided left ventricular injection ensures the accuracy so that every animal in this study developed brain metastases and no animal death was observed. The beauty of image-guided injection is that the path of needle penetration of skin and finally into the left ventricle can be monitored and adjusted under image, which is distinct from the manual procedure requiring strict anatomic landmarks to follow.

Current understanding...

Materials

Name	Company	Catalog Number	Comments
DMEM	HyClone	SH30022.01
Trypsin	Mediatech	25-051-C1
Automatic cell counter	BioRad	TC10
Isoflurane	Baxter International Inc.	1001936060
VisualSonics Vevo 770 High-Resolution Imaging System	Visual Sonics Inc.
9.4 T horizontal bore magnet with a Varian INOVA Unity system	Agilent
O.C.T Compound	Sakura Finetek USA	4583