Performing Colonoscopic-Guided Pinch Biopsies in Mice and Evaluating Subsequent Tissue Changes

Summary

Here, we provide a detailed description of the procedure to induce colonoscopic-guided pinch biopsies in mice and track wound closure in real time. Additionally, methods for the preparation of tissues for histological, immunohistochemical and molecular analyses of the wound bed are provided.

Abstract

Understanding the tissue and cellular changes that occur in the acute injury response as well as during the wound healing process is of paramount importance when studying diseases of the gastrointestinal (GI) tract. The murine colonic pinch biopsy model is a useful tool to define these processes. Additionally, the interplay between gut luminal content (e.g., microbes) and the colon can be studied. However, wound induction and the ability to track wound closure over time in a reliable manner can be challenging. Moreover, tissue preparation and orientation must be carried out in a standardized way to optimally interrogate histologic and molecular changes. Here, we present a detailed method describing biopsy-induced injury and the monitoring of wound closure through repeat colonoscopies. An approach is described that ensures consistent and reproducible measurements of wound size, the ability to collect the wound bed for molecular analyses as well as visualize the wound bed upon sectioning of tissues. The ability to successfully carry out these techniques allows for studies of the acute injury response, wound healing and luminal-host interactions within the colon.

Introduction

The gastrointestinal (GI) tract is a complex organ system given its multiple functions, host cell types (e.g. epithelial, immune, stromal, etc.) as well as trillions of microbes. In light of this complexity, diseases of the GI tract often involve the interplay of all of these factors. For example, inflammatory bowel diseases (IBD) are associated with cycles of inflammation and remission in the GI tract, involving the activation of inflammatory cells, dysbiosis, and epithelial repair^{1,2,3,4,5,6,7}. Having appropriate model systems to study IBD and other inflammatory conditions of the GI tract is critical for elucidating the pathogenesis of disease. Several models exist to study IBD pathogenesis including genetically engineered mice and the use of chemicals such as dextran sodium sulfate (DSS) in rodents^8,9,10. Limitations of these models include an inability to precisely control the induction of inflammation as well as difficulties in evaluating wound healing. Alternative methods to mimic aspects of IBD pathogenesis could prove useful for developing therapies.

Colonoscopic-guided pinch biopsies in mice offer a useful model system to study the pathogenesis of the inflammatory response, wound healing, as well as host-microbe interactions in the colon. This approach was first used as an experimental tool in 2009, which demonstrated its utility for studying the acute inflammatory response and wound healing in the gut¹¹. Subsequent studies utilized this technique to evaluate the roles of different signaling pathways as well as the gut microbiota, in colonic wound healing^{11,12,13,14,15,16,17,18}. More recently, our group used this model to investigate the importance of sphingosine-1-phosphate signaling and bacteria in the acute response to colonic injury¹⁹. Although useful, carrying out colonoscopic-guided pinch biopsies in mice and evaluating subsequent tissue changes can be technically challenging. For instance, perforation of the bowel can occur upon induction of injury and ensuring consistent measurements of the wound bed through serial colonoscopies can be difficult. Additionally, orienting the colonic tissue properly to visualize the wound bed for histological or immunohistochemical analyses can be challenging. Although some information does exist regarding these methods^18,20, a precise step-wise description of these techniques along will visual aids promises to enhance the reliability and broader utility of this model. Here, we present a detailed method to carry out colonoscopic-guided pinch biopsies in mice, track wound closure over time and prepare the tissue to enable histologic and molecular analyses of the wound bed. Creating a standard method to carry out these techniques can expand the use of this model to study previously uninvestigated mediators that are potentially important for GI inflammation and wound repair.

Protocol

All procedures described here were approved by the Institutional Animal Care and Use Committee of Weill Cornell Medicine.” To: “All procedures described here were approved by the Institutional Animal Care and Use Committees of Weill Cornell Medicine and Stony Brook University.

1. Colonoscopy and wound induction

1. Pre-assemble the components of the endoscope by first inserting the 1.9 mm rigid bore endoscope into the sheath (Figure 1A-B). Attach the air pump (to provide colonic insufflation) using the tubing provided, to the gas valve on the left side of the sheath next to the working channel (Figure 1C).
   NOTE: Although the lens described here is 0°, a 30° lens can also be used for this purpose.
2. Ensure that the working channel is in the open position and insert 3 Fr biopsy forceps through the working channel and advance it until the end of the sheath (while ensuring that it does not protrude out of the sheath) (Figure 1C). Attach the assembled endoscope to the light source and video imaging device per manufacturer’s instructions.
3.  Anesthetize the mouse with 5% isoflurane with oxygen in an induction chamber. Then move the mouse to an endoscopic staging platform containing a heating system (to prevent hypothermia) on its ventral side and maintain under anesthesia using a nose cone with 2% isoflurane with oxygen. Add vet ointment to the eyes to prevent dryness while under anesthesia. Ensure that the mouse is fully anesthetized by gently pinching the rear foot to test for a reflex.
   NOTE: Any strain or either sex of mice can be used with this technique; however, it is preferable that mice are at least 8 weeks of age so they are large enough for the procedure.
   1. Add vet ointment to the eyes to prevent dryness while under anesthesia.
   2. Ensure that the mouse is fully anesthetized by gently pinching the rear foot to test for a reflex.
4. Fill a 3 mL syringe with an attached rat gavage needle with room temperature phosphate-buffered saline (PBS). Insert needle approximately 1 cm into the mouse’s anus and gently infuse PBS to clear fecal material. Several fecal pellets should exit the mouse along with the PBS that was infused.
   NOTE: Instillation of an excessive volume of PBS can result in foam formation in the lumen which could obscure viewing of the lumen.
5. Insert the assembled endoscope 0.5 cm into the anus of the mouse. Advance the biopsy forceps into the lumen of the rectum until the full ‘jaws’ (including hinge) of the forceps are beyond the end of the sheath (as observed on the video monitor) (Supplemental Video 1). Turn the forceps 90° so that the jaws open in an east-west orientation (Supplemental Video 1).
6. To biopsy, open the forceps and advance approximately 1 cm, close the forceps and in one smooth motion quickly pull back on the forceps while leaving them closed (Supplemental Video 1).
   1. Avoid fully insufflating the colon when performing the biopsy. Therefore, leave the right side of the gas valve open during this step; although it should be noted that upon opening the forceps there is a risk of damaging the mucosa when the colon is in this position.

2. Visualizing and measuring the wound bed

1. Initiate video recording immediately after biopsy by pressing the foot pedal attached to the colonoscope recording device. Fully insufflate the colon by firmly pressing an index finger against the right side of the gas valve to completely cover the opening in order to force the air into the endoscope and thus into the colon.
   NOTE: Although this protocol describes the use of an air pump in which the air flow is manually controlled, a peristaltic pump with a controlled air supply can also be used.
2. Advance the forceps back out of the sheath, and into the rectal lumen while in the closed position (Supplemental Video 1). Place the forceps against the rectal wall immediately above the wound until the base of the jaws is aligned with the top edge of the viewing field (Figure 2 & Supplemental Video 1). Continue fully insufflating the colon until a clear view of the wound can be observed.
   NOTE: Care should be taken to extend the forceps far enough to reveal only the jaws of the forceps up to the base  for every mouse being examined in order to ensure a consistent distance between the lens of the endoscope and the lesion (Figure 2, white arrow).
3. If carrying out biopsies on multiple mice on the same day, remove the biopsied tissue of the previous mouse from the forceps (using the cleaning brush provided) and wipe down the lens sheath with 70% ethanol to clean it before inducing a wound in the next mouse.
   NOTE: Although this protocol describes carrying out a single biopsy per mouse, multiple biopsies can be performed on a single mouse provided the tissue taken from the prior biopsy is removed from the forceps in order to ensure a full biopsy can be taken on subsequent biopsies.
4. Place the mouse into a cage void of other mice and on top of a towel to keep the airway clear until it recovers from the anesthesia after completing the procedure. Monitor mouse to ensure that it recovers from the anesthesia as indicated by regaining activity.
   NOTE: Two people are required to induce the wound and visualize the wound bed on day 0 (one operating the endoscope and the other operating the biopsy forceps) but only one individual is needed for visualizing wounds on subsequent days (as described below).
5. Follow the same procedure for preparation of the mouse and colonoscopy for subsequent wound measurements (typically days 2, 4 and 6 following biopsy), as described above in sections 1.1-1.4, except for the induction of the wound.
6. Locate the wound bed on the video monitor at these time points after inserting the endoscope, and advance the biopsy forceps (in the closed position) to immediately above the wound bed, insufflate the colon and initiate video recording, as described in sections 2.1 and 2.2 (Figure 2).
   NOTE: It can be difficult to locate the wound bed more than 6 days following biopsy.
7. Advance the forceps into the lumen on these subsequent days to the same distance as on day 0 to ensure a consistent distance between the lens of the endoscope and the lesion across days. Ensuring a consistent distance between the lens and lesion will enhance the accuracy of measurements over time.
   NOTE: One individual can carry out measurements on these days (endoscope is operated with the right hand and the biopsy forceps are advanced with the left hand).
8. Once all measurements are completed, open the video recordings of the serial colonoscopies in video editing software that enables the creation of still shots from video.
9. Advance the video to a frame showing a point in time when the wound bed can be easily visualized, the closed forceps are above the wound bed and against the rectal wall and the wall is taut. Take a snapshot of this frame and code the file name to ensure that measurements of the wound beds are carried out in a blinded manner.
10. Open the images with coded file names in NIH ImageJ to quantify the size of the wound bed. Under the Analyze tab, select Set Measurements and check the Area box.
    1. Select the Freehand selections tool from the main menu bar and draw a perimeter around the wound (see Figure 2). Under the Analyze tab select Measure and the value of that measurement will automatically populate in the Results window.
11. Export the results into a spreadsheet after completing measurements for all images, by selecting Save As under the File tab within the Results window and changing the extension to become a spreadsheet file.
12. Calculate the size of the wound on days subsequent to the induction of the wound (i.e. days 2, 4 and 6) relative to the size on day 0 (immediately after wounding) in a spreadsheet. Accomplish this by dividing the size of the wound on each day by the size of the wound on day 0 and converting that value to a percentage.
    NOTE: Under normal conditions using this method of colonoscopic viewing, the greatest closure of the wound is observed after the first 2 days (~75% reduction in size) with more gradual closure on days 4 and 6 (~80% and ~95% reduction in size, respectively).

3. Collection of the wound bed for molecular analysis

1. Euthanize mouse using CO₂ asphyxiation followed by cervical dislocation (or equivalent technique) on the selected day following biopsy.
2. Harvest the distal region of the colon by opening the skin and abdominal muscle to expose the body cavity. Place closed scissors under the colon and gently lift to release it from the underlying mesentery and then cut the colon at its midpoint and at the anus to remove it from the mouse.
3. Flush fecal content using a rat gavage needle attached to a 20 mL syringe filled with ice-cold 1x PBS then lay down the colon onto filter paper.
4. Cut open the colon longitudinally on filter paper ensuring that the mesenteric side is face down against the filter paper. Apply 0.2% methylene blue to the mucosa using a squeeze pipet while tissue is still on the filter paper and then drain off excess methylene blue. View the colon under a dissecting microscope and locate the wound bed (Figure 3A).
5. Using 4 inch micro iris scissors, cut around the edge of the wound bed (Figure 3A, dashed circle) being careful not to cut into the muscle layer (unless the muscle is desired) and transfer the dissected wound bed to a tube using fine point tweezers for snap-freezing or desired storage method.
   NOTE: The amount of tissue collected in this manner is enough for extracting RNA for RNA-seq or equivalent analysis.

4. Preparation of tissue for histological analysis

1. Euthanize the mouse and harvest the colon as described in step 3.1-3.2.
2. Cut open the colon longitudinally on filter paper ensuring that the mesenteric side is face down against the filter paper. Gently apply 4% paraformaldehyde (or fixative of choice) using a squeeze pipet and cover the tissue with parafilm. Leave flat in a sealed container for 4-6 hours.
3. Transfer tissues to 70% ethanol for storage. When ready to process the tissues, remove parafilm and apply 0.2% methylene blue to the mucosa using a squeeze pipet while tissue is still on filter paper. Then drain off excess methylene blue.
4. View the colon under a dissecting microscope and locate the wound bed (Figure 3A). Using a scalpel with a #10 blade, cut directly through the center of the wound bed and continue cutting through the remainder of the colon in a straight line, such that the colon has been cut in half, length-wise (Figure 3A, black line).
5. Process the colon and then paraffin embed (either one or both sides that remain after cutting) such that the side that was cut by the scalpel (the side that was the center of wound bed before bisection) is face down in the paraffin. Proceed to cutting sections and staining for desired stain(s) or maker(s).
6. If cryosections are required for a given staining, harvest the colon as described in step 3.1 and open longitudinally on filter paper, ensuring that the mesenteric side is face down against the filter paper.
7. Bisect the wound bed within the freshly harvested colon as described in step 4.5 and embed the colon (either one or both sides that remain after cutting) such that the side that was cut by the scalpel is face down in a base mold half-filled with tissue freezing medium.
8. Secure the tissue in place with fine tweezers and place the base mold onto a metal plate on top of dry ice to harden the freezing medium. Once the bottom portion of the medium is frozen (and the tissue is held in place), release the tissue and fill the remaining volume of the base mold with freezing medium and place back onto dry ice.
   1. After the entire volume of freezing medium is frozen, transfer to a -80 °C freezer until sectioning.
9. For paraffin or frozen sections, cut and stain additional sections by H&E to ensure that the wound bed has been captured on the section before proceeding to study-specific staining. Figure 3B shows an example of a section in which the wound bed can be clearly observed.

Results

The small items (lens, sheath, biopsy forceps) needed to carry out biopsies are shown in Figure 1 along with indicators of proper assembly of these components. Figure 2 shows representative images of acceptable views of the wound bed in order to accurately quantify the size of the wound bed and closure rate of the wound. An example of an ex vivo view of the wound bed is shown in Figure 3A inclusive of indicators of the perimeter of ...

Discussion

Ensuring consistent and accurate biopsies as well as measurements of wound size are of paramount importance when attempting to effectively evaluate the rate of wound closure in this model. Therefore, several measures should be taken to be confident that the procedures are being correctly carried out. First, the depth of the biopsy must not be too shallow or deep. If too shallow, there will not be a sufficient window to evaluate wound closure. Figure 2 demonstrates an optimal biopsy depth and...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Biopsy forceps, 3 Fr	Karl Storz	61071ZJ
Coloview Tower system	Karl Storz	contact company
Examination sheath, 9 Fr, Kit	Karl Storz	61029DK
Hopkins telescope, 0', 1.9 mm x 10 cm	Karl Storz	64301AA
isofluorane	Covetrus	2905
methylene blue	Sigma-Aldrich	M9140
micro iris scissors	Integra	18-1619
NIH ImageJ	NIH	N/A	software available for free download from: https://imagej.nih.gov/ij/
Pawfly MA-60 aquarium pump	Amazon	N/A
scalpal with #10 blade	Hill-Rom	372610