A Novel Use of Three-dimensional High-frequency Ultrasonography for Early Pregnancy Characterization in the Mouse

Summary

Mice are widely used to study gestational biology. However, pregnancy termination is required for such studies which precludes longitudinal investigations and necessitates the use of large numbers of animals. Therefore, we describe a non-invasive technique of high-frequency ultrasonography for early detection and monitoring of post-implantation events in the pregnant mouse.

Abstract

High-frequency ultrasonography (HFUS) is a common method to non-invasively monitor the real-time development of the human fetus in utero. The mouse is routinely used as an in vivo model to study embryo implantation and pregnancy progression. Unfortunately, such murine studies require pregnancy interruption to enable follow-up phenotypic analysis. To address this issue, we used three-dimensional (3-D) reconstruction of HFUS imaging data for early detection and characterization of murine embryo implantation sites and their individual developmental progression in utero. Combining HFUS imaging with 3-D reconstruction and modeling, we were able to accurately quantify embryo implantation site number as well as monitor developmental progression in pregnant C57BL6J/129S mice from 5.5 days post coitus (d.p.c.) through to 9.5 d.p.c. with the use of a transducer. Measurements included: number, location, and volume of implantation sites as well as inter-implantation site spacing; embryo viability was assessed by cardiac activity monitoring. In the immediate post-implantation period (5.5 to 8.5 d.p.c.), 3-D reconstruction of the gravid uterus in both mesh and solid overlay format enabled visual representation of the developing pregnancies within each uterine horn. As genetically engineered mice continue to be used to characterize female reproductive phenotypes derived from uterine dysfunction, this method offers a new approach to detect, quantify, and characterize early implantation events in vivo. This novel use of 3-D HFUS imaging demonstrates the ability to successfully detect, visualize, and characterize embryo-implantation sites during early murine pregnancy in a non-invasive manner. The technology offers a significant improvement over current methods, which rely on the interruption of pregnancies for gross tissue and histopathologic characterization. Here we use a video and text format to describe how to successfully perform ultrasounds of early murine pregnancy to generate reliable and reproducible data with reconstruction of the uterine form in mesh and solid 3-D images.

Introduction

Recurrent early pregnancy loss is one of the most common complications after conception and affects approximately 1% of couples trying to conceive^1,2. The underlying mechanisms of early pregnancy loss are varied: from intrinsic embryonic abnormalities and maternal comorbidities to defects in endometrial receptivity^1,3,4. Because of their genetic tractability, mouse models have been widely utilized for investigations of early embryo implantation and pregnancy. Furthermore, the short gestational time of the mouse and the ability to perform large-scale studies have ensured the growing utility of the mouse in addressing key clinical questions in human reproductive medicine⁵. That said, the vast majority of murine experimental designs still require numerous dams to be euthanized on sequential gestational days to quantify and analyze implantation site location, number, size, and spacing patterns during pregnancy^6,7,8, thereby precluding longitudinal studies on the same animal.

In the clinic, ultrasound is a reliable and invaluable tool to monitor human fetal viability and development in a non-invasive manner^9,10,11. More recently, high-frequency ultrasound (HFUS) has begun to find limited applications in the mouse as a method for monitoring fetal viability and growth during pregnancy^12,13,14. The recent technological advances in ultrasound imaging have permitted the application of three-dimensional (3-D) data for visual reconstruction of animal organs and subsequent monitoring of pathologies^15,16,17. Use of this advanced imaging technology has markedly improved the power to detect smaller volume fluctuations, to reduce inter-animal variability, and to monitor the progression of a pathology or the efficacy of a therapeutic intervention¹⁷. While the primary utility of this technology has been to monitor malignancy progression in oncomouse models^15,16, 3-D HFUS imaging has only recently been used to quantitate and monitor the active growth of embryo implantation and fetal development in the mouse uterus¹⁸.

Here, we demonstrate how to perform HFUS imaging to produce 2-D and 3-D data to generate reconstructions of the early pregnant mouse uterus. We demonstrate the utility of this novel method to detect these early embryonic implantation events without the need for pregnancy termination, allowing researchers to collect data in a non-invasive manner.

Protocol

These studies were conducted in accordance with the Guide for the Care and Use of Laboratory Animals published by the National Institutes of Health and animal protocols approved by the Institutional Animal Care and Use Committee (IACUC) of Baylor College of Medicine under protocol number AN-4203.

1. Preparation of the Pregnant Mouse for Ultrasound

1. Timed mating
   1. Place the dam with a proven fertile male mouse overnight beginning after 1700. Separate dam and male by 0700 hours (h), regardless if vaginal plug is present, to ensure accurate dating of pregnancy.
      NOTE: The morning after mating is considered 0.5 day post coitum (d.p.c.).
2. Preparation for ultrasound
   1. Place the pregnant mouse in a sealed anesthesia induction container.
   2. Sedate with isoflurane (2%) inhaled anesthetic and oxygen (1 L/min) until the animal loses the righting reflex (approximately 1-2 min depending on the size of the mouse) and spontaneous movements are not observed (besides respiration).
   3. Place sedated mouse in supine position in nose cone with isoflurane (2%) inhaled anesthetic and oxygen (1 L/min). Apply ophthalmic ointment to the animal's eyes.
   4. With a cotton swab, apply depilatory cream to entire abdomen, sternum to vagina, and lateral to the flanks.
   5. Allow cream to remain for a maximum of 3 min, and then remove cream and hair with tissue. Ensure that all hair is removed, as any remaining hair will decrease image quality.

2. Preparation of the Ultrasound Stage

1. Turn on the transducer.
2. Attach 3-D motor stage motor stage to the transducer.
   1. Plug into 3D motor by connecting the 3D motor cable to the 3D motor connector on the rear panel. Attach the 3D motor system to the mounting system using the quick release post on the top to connect to the imaging station, and the quick release mount on the bottom to affix the transducer clamp.
3. Attach the probe to the transducer clamp.

3. Begin Imaging the Pregnant Mouse

1. Place mouse supine on the monitoring platform. The mouse continuously receives isoflurane anesthetic (between 1.5-2.5%) and oxygen (1 L/min) via the nose cone. Gently tape all paws to heart rate monitoring pads on the platform.
   1. Apply 1-2 mL of ultrasound transmission gel on abdomen.
2. Using the manual motor stage, position the ultrasound probe on the lower abdomen.
   1. Locate the bladder, which should appear as a fluid-filled dark circle just cephalad to the vaginal opening.
   2. Once the bladder is located, move the probe very slowly cephalad to visualize the pregnant uterus, which should appear as a cylindrical shape with round areas at pregnancy sites. This can be described as looking like pearls on a chain.
   3. Once the pregnant uterus has been identified, begin 2-D imaging.

4. The 2-D Ultrasound Imaging (Figure 1)

1. Once the pregnant uterus has been identified, begin at the pregnancy site closest to the bladder and slowly and sequentially move cephalad to determine number and location of pregnancy sites.
2. If the kidney, spleen, or liver are visualized, reposition the probe closer caudal (closer to the bladder) as the user has gone too far cephalad.
3. Image the contralateral uterine horn in the same manner.
4. Freeze the image when the ultrasound frame is in the center of the implantation/pregnancy site to save for later analysis and measurements.
   NOTE: It takes less than one second for the image to be frozen and saved for later analysis.
5. Measure implantation distance using the hyperechoic decidualization reaction as a marker by manually clicking on the "measure" tool first, and then clicking on the location of one implantation site. Next, drag the cursor to next implantation site and click to draw a line that the computer will automatically report its distance. The software will then report what the manual measurement is. This step is not computerized, but relies on the user to mark the distance between decidualized sites by drawing a line between the decidualized sites, which the program will provide a measurement for.
6. Measure implantation size, gestational sac size, and fetal pole size.

5. Fetal Heart Rate

NOTE: At 9.5 d.p.c., the fetal heart beat should be clearly visualized.

1. While keeping the probe very still, turn on the pulse wave Doppler and position this over the visible heartbeat.
2. Record the cardiac heart beat pulsations.
   NOTE: Apart from the heart, this procedure can also record pulsations in the umbilical cord.

6. 3-D Ultrasound Acquisition

1. After the pregnant uterus has been visualized on 2-D imaging, position the probe in an area that is in the approximate mid-point of the desired 3-D image. For example, if one were imaging an apple in 3-D, the probe should initially be placed where the apple core is predicted to be located (i.e. middle of object).
2. With the probe in a position in the middle of the desired image, obtain a 3-D acquisition. The 3-D motor stage will travel this distance across the uterus in a series of steps or frames, with the intention of capturing in entirety what the investigator desires.
3. Confirm that the intended structures are completely captured in the 3-D scanning before completing the real-time ultrasound portion. Save this 3-D information for post-processing at a later time. The total time for 2-D and 3-D ultrasound acquisition is approximately 10-20 minutes when performed by an experienced user.

7. 3-D Reconstitution Post-processing (Figure 2)

1. Load the desired data for 3-D image processing.
2. Choose "parallel and rotational methods", which will load all the 3D image frames into one 3-D "box" that the user will then trace the desired object in, frame-by-frame. Choose step size 0.08 mL. Begin at one end of the image block and scroll through to familiarize with the images that have been captured within space.
   1. Start at one end of the image and manually trace the outline of the object.
   2. Scroll to next 2-D image slice or "frame" and manually trace the outline of the object.
   3. Continue this process until all frames have been manually annotated/traced by the user.
   4. Click "finish" to obtain the 3-D image and total volume calculations.
3. Choose between mesh and solid overlay, which is an arrow in the top left corner.
4. Choose to keep or remove the surrounding ultrasound image information for clarity. Each 3-D reconstruction may take between 10 and 20 min.

8. Post-procedural Care

1. When the ultrasound is complete, turn off the anesthesia gas, remove the mouse from the platform and gently wipe and wash away any ultrasound gel from the animal.
2. Place the mouse back in the cage in a prone position in a padded area. Monitor until the animal is awake and moving spontaneously.

Results

As demonstrated in Figure 1, the high frequency ultrasound can detect implantation site development beginning as early as the 5.5 d.p.c time point. Using the lighter hyperechoic decidualized endometrium as a marker of implantation sites at 6.5 d.p.c allows the number of implantation sites and spacing of these sites to be quantified. As the pregnancy progresses to 7.5 d.p.c., a darker hypoechoic gestational sac and fetal pole are also easily identifiable.

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Discussion

This novel use of 3-D HFUS imaging demonstrates the ability to successfully detect, visualize, and characterize embryo-implantation sites during early murine pregnancy in a non-invasive manner. The technology offers a significant improvement over current methods, which rely on the interruption of pregnancies for gross tissue and histopathologic characterization. However it should be noted that histological methods would still be considered more optimal when characterization at a more magnified and more cellular level is ...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
VisualSonics Vevo 2100 Ultrasound Imaging Platform/Machine	VisualSonics, inc.	VS-11945
Vevo Imaging Station	VisualSonics, inc.	SA-11982
Aquasonic 100 Ultrasound Transmission Gel	Parker	#SKU PLI 01-08
Isoflurane (IsoThesia) 100mL bottle	Henry Shein	#29404
PuraLubenAnimal Ophthalmic Ointment	Dechra	#12920060